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s-adenosylmethionine

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Description

S-adenosylmethionine (SAMe) is a naturally occurring compound found in the body. It plays a crucial role in various metabolic processes, including the synthesis of neurotransmitters like dopamine, serotonin, and norepinephrine, as well as the methylation of DNA, RNA, and proteins. SAMe is synthesized from methionine and ATP in a reaction catalyzed by the enzyme methionine adenosyltransferase. It has been investigated for its potential therapeutic benefits in conditions such as depression, osteoarthritis, and liver disease. Its effects are attributed to its ability to increase levels of neurotransmitters, reduce inflammation, and protect cells from damage. Studies exploring its potential for treating various conditions continue to be conducted.'

(R)-S-adenosyl-L-methionine : An S-adenosyl-L-methionine that has R-configuration. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

S-adenosyl-L-methionine zwitterion : A zwitterionic tautomer of S-adenosyl-L-methionine arising from shift of the proton from the carboxy group to the amino group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

(R)-S-adenosyl-L-methionine zwitterion : An S-adenosyl-L-methionine zwitterion that has R-configuration; major species at pH 7.3. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

(S)-S-adenosyl-L-methionine zwitterion : An S-adenosyl-L-methionine zwitterion that has S-configuration; major species at pH 7.3. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

S-adenosyl-L-methionine : A sulfonium compound that is the S-adenosyl derivative of L-methionine. It is an intermediate in the metabolic pathway of methionine. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

acylcarnitine: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

S-adenosyl-L-methioninate : A sulfonium betaine that is a conjugate base of S-adenosyl-L-methionine obtained by the deprotonation of the carboxy group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

5-deazafolic acid: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID24762165
CHEBI ID59789
CHEBI ID142094
CHEBI ID142093
MeSH IDM0019322
PubMed CID34755
CHEMBL ID1088977
CHEMBL ID1235831
CHEBI ID67040
SCHEMBL ID1300198
MeSH IDM0019322
PubMed CID135460994
SCHEMBL ID9838338
MeSH IDM0019322

Synonyms (118)

Synonym
(s,s)-adomet
(r)-s-adenosyl-l-methionine
(r,s)-adomet
adenosylmethionine
s-adenosyl-l-methionine
SAM ,
2-s-adenosyl-l-methionine
adomet
(s)-s-adenosyl-l-methionine
s-adenosyl-methionine
S-ADENOSYLMETHIONINE ,
CHEBI:59789
[(3s)-3-azaniumyl-3-carboxylatopropyl](5'-deoxyadenosin-5'-yl)(methyl)sulfonium
s-adenosyl-l-methionine zwitterion
(r)-s-adenosyl-l-methionine zwitterion
(r,s)-s-adenosyl-l-methionine zwitterion
(s,s)-adomet zwitterion
(s,s)-s-adenosyl-l-methionine zwitterion
(s)-s-adenosyl-l-methionine zwitterion
CHEBI:142094
(r,s)-adomet zwitterion
CHEBI:142093
139517-02-5
(2s)-4-[[(2s,3s,4r,5r)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl-methylsulfonio]-2-azaniumylbutanoate
16-denyprasteroneacetate
AC-19717
same
adenosine, 5'-(((3s)-3-amino-3-carboxypropyl)methylsulfonio)-5'-deoxy-, inner salt
einecs 249-946-8
methionine, s-adenosyl-
adenosine, 5'-((l-3-amino-3-carboxypropyl)methylsulfonio)-5'-deoxy-, hydroxide, inner salt
17176-17-9
active methionine
methionine, s-adenosyl- (6ci) active methionine
ccris 7130
s amet
(3s)-5'-[(3-amino-3-carboxylatopropyl)methylsulphonio]-5'-deoxyadenosine
adenosine, 5'-[(3-amino-3-carboxypropyl)methylsulfonio]-5'-deoxy-, hydroxide, inner salt, (3s)-
l-s-adenosylmethionine
ademetionine
(3s)-5'-[(3-amino-3-carboxylatopropyl)methylsulphonio]-5'-deoxyadenosine inner salt
s-(5'desoxyadenosin-5'yl)-l-methionine
adenosine, 5'-[(l-3-amino-3-carboxypropyl)methylsulfonio]-5'-deoxy-, hydroxide, inner salt (8ci)
l-methionine, s-adenosyl-
donamet
methioninyladenylate
adenosine, 5'-[[(3s)-3-amino-3-carboxypropyl)methylsulfonio]-5'-deoxy-, inner salt
[14cooh]adomet
s-adenosyl-l-[carboxy-14c]methionine
(2s)-2-amino-4-({[(2s,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}(methyl)sulfanylium)butanoate
bdbm28422
C00019
29908-03-0
adenosine, 5'-((3-amino-3-carboxypropyl)methylsulfonio)-5'-deoxy-, inner salt, (3s)-
[(3s)-3-amino-4-hydroxy-4-oxo-butyl]-[[(2s,3s,4r,5r)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl]-methyl-sulfonium
sam-e
DB00118
(3s)-5'-((3-amino-3-carboxylatopropyl)methylsulphonio)-5'-deoxyadenosine
s. amet
acylcarnitine
(2s)-2-amino-4-[[(2s,3s,4r,5r)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl-methylsulfonio]butanoate
msi-195
transmetil
chebi:67040 ,
CHEMBL1088977
CHEMBL1235831 ,
SCHEMBL1300198
AKOS015963176
unii-7lp2mpo46s
ademetionine [inn]
7lp2mpo46s ,
[(3s)-3-amino-3-carboxylatopropyl](5'-deoxyadenosin-5'-yl)(methyl)sulfonioacetate
s-adenosyl-l-methioninate
s-adenosylmethionine [vandf]
ademetionine [who-dd]
5'-((3s)-(3-amino-3-carboxypropyl)methylsulfonio)-5'-deoxyadenosine inner salt
ademetionine [mart.]
s-adenosylmethionine [mi]
s-(5'-desoxyadenosin-5'-yl)-l-methionine
HY-B0617
(r,s)-s-adenosyl-l-methionine
(s,s)-s-adenosyl-l-methionine
unii-k093c397ul
unii-6ez5466zux
6EZ5466ZUX ,
91279-78-6
78548-84-2
adenosine, 5'-((s)-((3s)-3-amino-3-carboxypropyl)methylsulfonio)-5'-deoxy-, inner salt
ademetionine, (r)-
s,s-adenosylmethionine
adenosine, 5'-((r)-((3s)-3-amino-3-carboxypropyl)methylsulfonio)-5'-deoxy-, inner salt
r,s-adenosylmethionine
K093C397UL ,
ademetionine, (s)-
DTXSID6032019
(2s)-2-amino-4-((((2s,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)(methyl)sulfonio)butanoate
AS-57895
(2s)-2-amino-4-({[(2s,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}(methyl)sulfaniumyl)butanoate
NCGC00485915-01
MEFKEPWMEQBLKI-AIRLBKTGSA-N
s-adenosyl-l-methionine;s-adenosyl methionine;same;adomet
(2s)-2-amino-4-[{[(2s,3s,4r,5r)-5-(6-amino-9h-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}(methyl)sulfonio]butanoate (non-preferred name)
s-adenosyl-l-methioninate (deprotonated carboxy group)
Q27135598
CCG-268635
Q27281766
(r)-ademetionine
Q27264758
(s)-ademetionine
s-adenosyl-l-methionine hcl
EN300-7431717
ademetionine (mart.)
AKOS040750137
bdbm50585598
5-deazafolic acid
SCHEMBL9838338
n-[(4-{[(2-amino-4-oxo-1,4-dihydropyrido[2,3-d]pyrimidin-6-yl)methyl]amino}phenyl)carbonyl]-l-glutamic acid
Q27459797

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" We first tested the hypothesis of a toxic effect of MeSAdo in the conditions of growth experiments: we could not demonstrate any toxic effect of MeSAdo on the synthesis of macromolecules, nor any toxicity mediated by polyamines or pyrimidine starvation, and we found that the growth of CCL39 cells was strictly dependent on the supply of exogenous methionine."( Methylthioadenosine toxicity and metabolism to methionine in mammalian cells.
Augé, J; Christa, L; Kersual, J; Pérignon, JL, 1988
)
0.27
" Treatment was considered to be without adverse effect upon any of the reproductive parameters examined on either F0 or on the untreated F1 generations."( Reproductive toxicity studies of ademetionine.
Barton, SJ; Clark, R; Cozens, DD; Gibson, WA; Hughes, EW; Masters, RE; Offer, JM; Perkin, CJ; Stramentinoli, G, 1988
)
0.27
"5 rat embryos L-homocysteine was not toxic at 1- and 2-mM concentrations."( Prevention of neural tube defects by and toxicity of L-homocysteine in cultured postimplantation rat embryos.
Blom, HJ; Copius Peereboom-Stegeman, JH; Deabreu, RA; Eskes, TK; Noordhoek, J; Trijbels, FJ; Vanaerts, LA, 1994
)
0.29
"Rats were fed toxic levels of methionine with or without simultaneous dietary supplements of glycine and serine."( Methionine toxicity in the rat in relation to hepatic accumulation of S-adenosylmethionine: prevention by dietary stimulation of the hepatic transsulfuration pathway.
Alakuijala, L; Eloranta, TO; Korhonen, VP; Regina, M; Smith, TK, 1993
)
0.29
"L-dopa may be toxic to dopamine neurons, possibly due to catechol-autoxidation."( COMT-dependent protection of dopaminergic neurons by methionine, dimethionine and S-adenosylmethionine (SAM) against L-dopa toxicity in vitro.
Bottiglieri, T; Bressman, S; Di Rocco, A; Prikhojan, A; Rempel, N; Werner, P; Yahr, MD, 2001
)
0.31
"The outcomes considered were pain, functional limitation, and adverse effects."( Safety and efficacy of S-adenosylmethionine (SAMe) for osteoarthritis.
Agelli, M; Bausell, RB; Berman, BM; Lee, WL; Soeken, KL, 2002
)
0.31
" However, those treated with SAMe were less likely to report adverse effects than those receiving NSAIDs."( Safety and efficacy of S-adenosylmethionine (SAMe) for osteoarthritis.
Agelli, M; Bausell, RB; Berman, BM; Lee, WL; Soeken, KL, 2002
)
0.31
"SAMe appears to be as effective as NSAIDs in reducing pain and improving functional limitation in patients with OA without the adverse effects often associated with NSAID therapies."( Safety and efficacy of S-adenosylmethionine (SAMe) for osteoarthritis.
Agelli, M; Bausell, RB; Berman, BM; Lee, WL; Soeken, KL, 2002
)
0.31
" Adverse events were significantly less in patients treated with SAMe compared to those treated with IMI."( A double-blind, randomized parallel-group, efficacy and safety study of intramuscular S-adenosyl-L-methionine 1,4-butanedisulphonate (SAMe) versus imipramine in patients with major depressive disorder.
Chiaie, RD; Pancheri, P; Scapicchio, P, 2002
)
0.31
"S-Adenosyl-l-methionine (SAM) has been shown to be hepatoprotective against many toxic agents."( S-adenosyl-L-methionine attenuates hepatotoxicity induced by agonistic Jo2 Fas antibody following CYP2E1 induction in mice.
Cederbaum, AI; Wang, X, 2006
)
0.33
"To review the complementary medicines routinely encountered in psychiatric practice, their effectiveness, potential adverse effects and interactions."( Complementary medicines in psychiatry: review of effectiveness and safety.
Priebe, S; Turner, T; Werneke, U, 2006
)
0.33
" Fumonisin B(1) (FB(1)) is the most toxic and prevalent fumonisin detected in corn and corn-based foods."( S-adenosylmethionine or 5'-methylthioadenosine are unable to prevent fumonisin B1 hepatotoxicity in mice despite increased oxidation in liver.
He, Q; Sharma, RP; Suzuki, H,
)
0.13
" Treatment of the toxic hepatitis with heptral increased the level of cytochrome P450, cytochrome b5, glutation activity of glutationetranspherase glutathione and reduced content of homocysteine."( [Efficacy and safety of heptral, vitamin B6 and folic acid during toxic hepatitis induced by CCL4].
Antelava, NA; Gogoluari, LI; Gogoluari, MI; Okudzhava, MV; Pirtskhalaĭshvili, NN, 2007
)
0.34
" Since S-adenosylmethionine (SAMe) is the primary source of the sulfur atom in glutathione, UPLC/MS and NMR were used to evaluate metabolites involved with the transulfuration pathway in urine samples collected during studies of eight liver toxic compounds in Sprague-Dawley rats."( Evaluations of the trans-sulfuration pathway in multiple liver toxicity studies.
Beger, RD; Chen, M; Dragan, Y; Holland, RD; Schnackenberg, LK; Sun, J; Tong, W; Welsh, W, 2009
)
0.35
" Our results show that exogenous SAM (10-50microM) rescues cells from the toxic effects of 6-MP (5microM) by delaying the onset of apoptosis."( S-adenosylmethionine regulates thiopurine methyltransferase activity and decreases 6-mercaptopurine cytotoxicity in MOLT lymphoblasts.
Karas Kuzelicki, N; Milek, M; Mlinaric-Rascan, I; Smid, A, 2009
)
0.35
" The incidence of pruritus and adverse effects as well as biochemical parameters in all the patients and compared between the 2 groups."( [Efficacy and safety of ademetionine for treatment of drug-induced liver disease in children].
Chen, DW; Dong, Y; Gan, Y; Jia, WZ; Tang, HM; Wang, LM; Xu, ZQ; Zhang, HF; Zhu, SS, 2010
)
0.36
"Intravenous administration of ademetionine is safe in children with DILD and it can effectively alleviate pruritus, promote the recovery of various biochemical parameters and fasten liver functional recovery in these children."( [Efficacy and safety of ademetionine for treatment of drug-induced liver disease in children].
Chen, DW; Dong, Y; Gan, Y; Jia, WZ; Tang, HM; Wang, LM; Xu, ZQ; Zhang, HF; Zhu, SS, 2010
)
0.36
" By comparing the sensitivity to selenomethionine of mutants impaired in the sulfur amino acid pathway, we excluded a toxic effect of Se-adenosylmethionine, Se-adenosylhomocysteine, or of any compound in the methionine salvage pathway."( Trans-sulfuration Pathway Seleno-amino Acids Are Mediators of Selenomethionine Toxicity in Saccharomyces cerevisiae.
Blanquet, S; Dauplais, M; Lazard, M; Plateau, P, 2015
)
0.42
" Oxidative stress also is a side effect of dideoxynucleoside antiretrovirals (NRTI) and is observed in NRTI-induced cardiomyopathy."( AZT-induced mitochondrial toxicity: an epigenetic paradigm for dysregulation of gene expression through mitochondrial oxidative stress.
Fields, E; Jiao, Z; Koczor, CA; Lewis, W; Ludaway, T; Russ, R, 2015
)
0.42
" Of the various high throughput technologies available to detect global methylation profile, development of LINE-1 methylation index shall provide a cost effect-screening tool to detect epimutagenic events in the wake of toxic exposure in a large number of individuals."( Arsenic toxicity and epimutagenecity: the new LINEage.
Bhattacharjee, P; Giri, AK; Paul, S, 2017
)
0.46
" However, it has considerable adverse effects that may cause public health burden."( Enhancement of safety and immunogenicity of the Chinese Hu191 measles virus vaccine by alteration of the S-adenosylmethionine (SAM) binding site in the large polymerase protein.
Hao, X; Huang, YW; Li, J; Liu, R; Lu, M; Wang, B; Wang, Y; Yang, Y; Zhao, Z; Zhou, D, 2018
)
0.48
"Drug-induced liver injury (DILI) is a rare but serious adverse event that can progress to acute liver failure (ALF)."( Therapeutic Management of Idiosyncratic Drug-Induced Liver Injury and Acetaminophen Hepatotoxicity in the Paediatric Population: A Systematic Review.
Aithal, GP; Alvarez-Alvarez, I; Andrade, RJ; Arikan, C; Atallah, E; Lucena, MI; Medina-Caliz, I; Niu, H, 2022
)
0.72
" We examined whether metabolic profiles can predict adverse events in patients undergoing coronary artery bypass grafting."( Metabolic profiles predict adverse events after coronary artery bypass grafting.
Craig, DM; Granger, CB; Hauser, ER; Haynes, C; Hughes, GC; Kraus, WE; Muehlbauer, MJ; Newby, LK; Newgard, CB; Sebek, JK; Shah, AA; Shah, SH; Stevens, RC, 2012
)
0.38
"4%) experienced an adverse event."( Metabolic profiles predict adverse events after coronary artery bypass grafting.
Craig, DM; Granger, CB; Hauser, ER; Haynes, C; Hughes, GC; Kraus, WE; Muehlbauer, MJ; Newby, LK; Newgard, CB; Sebek, JK; Shah, AA; Shah, SH; Stevens, RC, 2012
)
0.38
"Metabolic profiles are independently associated with adverse outcomes after coronary artery bypass grafting."( Metabolic profiles predict adverse events after coronary artery bypass grafting.
Craig, DM; Granger, CB; Hauser, ER; Haynes, C; Hughes, GC; Kraus, WE; Muehlbauer, MJ; Newby, LK; Newgard, CB; Sebek, JK; Shah, AA; Shah, SH; Stevens, RC, 2012
)
0.38
" The disturbance of cholesterol biosynthesis could have adverse impact on fatty acid metabolism, consequently induce the decrease of carnitine and increase of acylcarnitines in treated groups."( [Hepatotoxicity of perfluorooctanoic acid in human hepatocytes using metabonomics].
Peng, S; Shen, H; Yan, L; Zhang, J, 2012
)
0.38
" In the following study, the relationship of acylcarnitines with other known indicators of APAP toxicity was examined in children receiving low-dose (therapeutic) and high-dose ('overdose' or toxic ingestion) exposure to APAP."( Targeted liquid chromatography-mass spectrometry analysis of serum acylcarnitines in acetaminophen toxicity in children.
Beger, RD; Bhattacharyya, S; Gill, P; James, LP; Kearns, GL; Letzig, LG; Marshall, JD; Pence, L; Reed, MD; Simpson, PM; Sullivan, JE; Van Den Anker, JN; Yan, K, 2014
)
0.4
"Peripheral neuropathy (PN) is a dose-limiting, painful adverse reaction associated with the use of paclitaxel."( Cell metabolomics analyses revealed a role of altered fatty acid oxidation in neurotoxicity pattern difference between nab-paclitaxel and solvent-based paclitaxel.
Chang, LC; Huang, JW; Kuo, CH; Kuo, HC; Shih, JY; Tsai, TW, 2021
)
0.62

Pharmacokinetics

ExcerptReferenceRelevance
" Pharmacokinetic parameters were estimated according to an open two-compartment model."( Pharmacokinetics of S-adenosyl-L-methionine in healthy volunteers.
Cortellaro, M; Giulidori, P; Moreo, G; Stramentinoli, G, 1984
)
0.27
"A pharmacokinetic study based on the distribution of radioactivity from the double labelled S-adenosyl-L-methionine (SAM) has been carried out by oral administration of the liposoluble stable salt [methyl-(14)C, 8-(3)H]SAM N-ole-1-oyltaurate to rats."( S-adenosyl-L-methionine N-ole-1-oyltaurate: pharmacokinetic of the orally administered salt in rats.
Cartenì, M; De Rosa, A; De Rosa, M; Morana, A; Parlato, M, 2001
)
0.31
" Time-efficacy calculations showed that acute oral administration of SAMe in both the nutraceutical and the pharmaceutical dose induced the pharmacodynamic peak effect in the first hour with a subsequent decline."( Double-blind, placebo-controlled pharmacodynamic studies with a nutraceutical and a pharmaceutical dose of ademetionine (SAMe) in elderly subjects, utilizing EEG mapping and psychometry.
Anderer, P; Arnold, O; Assandri, A; Corrado, M; di Padova, C; Saletu, B; Saletu-Zyhlarz, GM, 2005
)
0.33
" Despite being widely used as a dietary supplement with claimed benefits for numerous conditions, there is little information about the pharmacokinetic properties of exogenous SAMe."( Pharmacokinetic properties of S-adenosylmethionine after oral and intravenous administration of its tosylate disulfate salt: a multiple-dose, open-label, parallel-group study in healthy Chinese volunteers.
Du, YX; Fawcett, JP; He, Y; Tang, LL; Wang, GJ; Yang, J, 2009
)
0.35
"One aim of this study was to characterize the pharmacokinetic properties of SAMe after administration of single and multiple doses of orally and intravenously administered SAMe tosylate disulfate (STD) in healthy male and female Chinese volunteers."( Pharmacokinetic properties of S-adenosylmethionine after oral and intravenous administration of its tosylate disulfate salt: a multiple-dose, open-label, parallel-group study in healthy Chinese volunteers.
Du, YX; Fawcett, JP; He, Y; Tang, LL; Wang, GJ; Yang, J, 2009
)
0.35
" The assay was used to study the pharmacokinetic properties of SAMe."( Pharmacokinetic properties of S-adenosylmethionine after oral and intravenous administration of its tosylate disulfate salt: a multiple-dose, open-label, parallel-group study in healthy Chinese volunteers.
Du, YX; Fawcett, JP; He, Y; Tang, LL; Wang, GJ; Yang, J, 2009
)
0.35
" None of the between-sex differences in SAMe pharmacokinetic properties were significant."( Pharmacokinetic properties of S-adenosylmethionine after oral and intravenous administration of its tosylate disulfate salt: a multiple-dose, open-label, parallel-group study in healthy Chinese volunteers.
Du, YX; Fawcett, JP; He, Y; Tang, LL; Wang, GJ; Yang, J, 2009
)
0.35
"In this small study in healthy Chinese volunteers, there were no significant differences in the pharmacokinetic parameters of SAMe between men and women or between single- and multiple-dose administration of STD 1000 mg administered orally or intravenously."( Pharmacokinetic properties of S-adenosylmethionine after oral and intravenous administration of its tosylate disulfate salt: a multiple-dose, open-label, parallel-group study in healthy Chinese volunteers.
Du, YX; Fawcett, JP; He, Y; Tang, LL; Wang, GJ; Yang, J, 2009
)
0.35
" The present research reports on a Phase 1 study to (i) determine the safety of single doses of MSI-195 (ii) to determine the dose proportionality of MSI-195 at doses of 400, 800 and 1600 mg (iii) determine the pharmacokinetics of MSI-195 compared with a commercial reference product (SAM-e Complete™) over 24 h and (iv) to determine the effect of food on the pharmacokinetic profile of MSI-195 in human subjects."( Pharmacokinetic study of a novel oral formulation of S-adenosylmethionine (MSI-195) in healthy subjects: dose escalation, food effect and comparison to a commercial nutritional supplement product.
Cameron, BR; Ferreira, L; MacDonald, ID, 2020
)
0.56
"This study was a pharmacokinetic and safety evaluation of MSI-195 and a commercial comparator broken into two stages."( Pharmacokinetic study of a novel oral formulation of S-adenosylmethionine (MSI-195) in healthy subjects: dose escalation, food effect and comparison to a commercial nutritional supplement product.
Cameron, BR; Ferreira, L; MacDonald, ID, 2020
)
0.56
" The product was administered orally to rats and pharmacokinetic parameters were evaluated by comparing the results with that obtained by administering the SAM tosylated form (SAM PTS)."( Pharmacokinetic properties of a novel formulation of S-adenosyl-L-methionine phytate.
Cavallaro, RA; d'Erme, M; Fanelli, S; Fontana, M; Francioso, A; Lendaro, E; Miraglia, N; Mosca, L, 2021
)
0.62
" The objective of this study was to evaluate the pharmacokinetic profile of SAMe enteric-coated tablets and to assess its food impact and safety in healthy Chinese subjects."( Pharmacokinetics and food impact assessment of ademetionine enteric-coated tablet as an endogenous substance drug in healthy Chinese volunteers.
Jin, M; Lin, H; Liu, H; Tang, L; Tong, Y; Wang, K; Yao, Y; Zhang, J, 2022
)
0.72
" Relevant pharmacokinetic data from subjects administered the reference formulation will be disclosed and utilized in this thesis."( Pharmacokinetics and food impact assessment of ademetionine enteric-coated tablet as an endogenous substance drug in healthy Chinese volunteers.
Jin, M; Lin, H; Liu, H; Tang, L; Tong, Y; Wang, K; Yao, Y; Zhang, J, 2022
)
0.72
"The pharmacokinetic profile of SAMe enteric-coated tablets in healthy Chinese subjects was partially complemented in this study."( Pharmacokinetics and food impact assessment of ademetionine enteric-coated tablet as an endogenous substance drug in healthy Chinese volunteers.
Jin, M; Lin, H; Liu, H; Tang, L; Tong, Y; Wang, K; Yao, Y; Zhang, J, 2022
)
0.72
" Betaine has been used for more than 30 years in pyridoxine non-responsive cystathionine beta-synthase (pnrCBS) and cobalamin C (cblC) deficiencies to lower the hyperhomocysteinemia, although little is known about the optimal therapeutic dosage and its pharmacokinetic in these patients."( Efficacy and pharmacokinetics of betaine in CBS and cblC deficiencies: a cross-over randomized controlled trial.
Alberti, C; Benoist, JF; de Baulny, HO; Feillet, F; Garcia-Segarra, N; Guilmin-Crépon, S; Haignere, J; Imbard, A; Kaguelidou, F; Kuster, A; Magréault, S; Perronneau, I; Schiff, M; Schlemmer, D; Toumazi, A, 2022
)
0.72

Compound-Compound Interactions

ExcerptReferenceRelevance
"Hepato- and endothelioprotective action of runihol and ademetionine in 66 male rats with liver disease induced by essential and second-line antituberculosis drugs in combination with alcohol were studied."( [Hepato- and endothelioprotective action of runihol and ademetionine in experimental liver injury induced by TB drugs in combination with alcohol].
Artyushkova, EB; Dudka, VT; Sukhanov, DS,
)
0.13
" Metabolic therapy may be recommended for patients with chronic hepatitis C in combination with type 2 diabetes in case of SAVT, and at its contraindications or intolerance."( [Correction of dyslipidemia in patients with chronic hepatitis C, combined with diabetes type 2].
Boldizhar, P; Derbak, M, 2014
)
0.4
" cerevisiae CGMCC 2842 (wild type), improvement of methionine and ATP availability through MET6 and SAM2 co-expression combined with sodium citrate feeding was investigated here."( Improving methionine and ATP availability by MET6 and SAM2 co-expression combined with sodium citrate feeding enhanced SAM accumulation in Saccharomyces cerevisiae.
Chen, H; Dou, J; Wang, Z; Zhou, C, 2016
)
0.43

Bioavailability

S-adenosylmethionine (MSI-195) has been developed for life science application. Homocysteine levels are regulated by folate bioavailability.

ExcerptReferenceRelevance
" Exogenous SAMe is stable in digestive juices and, although well absorbed orally, bioavailability is reduced because of a significant first pass effect in the liver."( Metabolism of exogenous S-adenosyl-L-methionine in patients with liver disease.
Blake, JC; Burroughs, AK; Kaye, GL, 1990
)
0.28
"A perfusion technique was utilized to assess the rate of absorption and metabolism of L-methionine by livers isolated from rats fed a diet deficient in zinc."( Effect of zinc deficiency on methionine metabolism, methylation reactions and protein synthesis in isolated perfused rat liver.
Duerre, JA; Wallwork, JC, 1985
)
0.27
" There were no statistically significant differences in the cumulative amount absorbed of drug and the absorption rate in the presence or absence of Madopar."( Lack of an effect of Madopar on the disposition of tolcapone and its 3-O-methylated metabolite in rats.
Fukazawa, H; Funaki, T; Kuruma, I; Onodera, H; Tagami, C; Tsukamoto, Y; Ushiyama, N, 1995
)
0.29
" The partial beneficial effects might also be explained by the age-related limited bioavailability of exogenous SAMe, a finding, to our knowledge, not yet reported elsewhere."( Biochemical analysis of myelin lipids and proteins in a model of methyl donor pathway deficit: effect of S-adenosylmethionine.
Bellasio, R; Bianchi, R; Calzi, F; Savaresi, S; Sciarretta-Birolo, R; Tacconi, MT; Tsankova, V, 1999
)
0.3
" Homocysteine levels are regulated by folate bioavailability and also by the methyl donor S-adenosylmethionine (SAM) and its metabolite S-adenosylhomocysteine (SAH)."( Endothelial dysfunction and elevation of S-adenosylhomocysteine in cystathionine beta-synthase-deficient mice.
Arning, E; Bottiglieri, T; Dayal, S; Faraci, FM; Heistad, DD; Lentz, SR; Maeda, N; Malinow, MR; Sigmund, CD, 2001
)
0.31
" Other effects of homocysteine include: impaired generation and decreased bioavailability of endothelium-derived relaxing factor/nitric oxide; interference with many transcription factors and signal transduction; oxidation of low-density lipoproteins; lowering of endothelium-dependent vasodilatation."( [Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data].
Favier, A; Galan, P; Guilland, JC; Hercberg, S; Potier de Courcy, G, 2003
)
0.32
" Polyenylphosphatidylcholine (PPC), an antioxidant phosphatidylcholine mixture extracted from soybeans, 50% of which consists of the highly bioavailable dilinoleoylphosphatidylcholine, restores phospholipids of the damaged membranes and reactivates their enzymes, including phosphatidylethanolamine methyltransferase, needed for phospholipid regeneration."( New concepts of the pathogenesis of alcoholic liver disease lead to novel treatments.
Lieber, CS, 2004
)
0.32
" Although oral SAMe appears to be absorbed across the intestinal mucosa, its systemic bioavailability is low."( S-adenosyl-L-methionine: transcellular transport and uptake by Caco-2 cells and hepatocytes.
McMillan, JM; Walle, T; Walle, UK, 2005
)
0.33
" It is apparent that SMM in foods and feeds has methylation bioactivity, and this has implications for proper assessment of dietary Met and choline requirements as well as their bioavailability in foods and feeds."( Dietary S-methylmethionine, a component of foods, has choline-sparing activity in chickens.
Augspurger, NR; Baker, DH; Garrow, TA; Scherer, CS, 2005
)
0.33
" Chronic ethanol consumption could affect the bioavailability of amino acids such as methionine."( Hepatic S-adenosylmethionine after maternal alcohol exposure on offspring rats.
Artillo, R; Carreras, O; Murillo, ML; Murillo-Fuentes, ML; Ubeda, N; Varela-Moreiras, G, 2005
)
0.33
" Because of the rather low bioavailability of most polyphenolic compounds, how much of an effect dietary polyphenols would have on DNA methylation in humans is not clear."( Dietary polyphenols may affect DNA methylation.
Chen, D; Fang, M; Yang, CS, 2007
)
0.34
" Compared with other forms of folates, 5-methyltetrahydrofolate (L-methylfolate or 5-MTHF) may represent a preferable treatment option for MDD given its greater bioavailability in patients with a genetic polymorphism, and the lower risk of specific side effects associated with folic acid."( Folates and S-adenosylmethionine for major depressive disorder.
Cassiello, CF; Iovieno, N; Papakostas, GI, 2012
)
0.38
"We investigated the effects of folate-enriched egg yolk powder on folate and homocysteine levels in plasma and liver of rats fed the folate- and choline-deficient diet to determine bioavailability in vivo."( The beneficial effect of folate-enriched egg on the folate and homocysteine levels in rats fed a folate- and choline-deficient diet.
Awaji, H; Horie, K; Kim, M; Nakata, R; Sugiyama, A, 2012
)
0.38
" GNMT expression in vivo improves folate retention and bioavailability in the liver."( Regulation of Folate-Mediated One-Carbon Metabolism by Glycine N-Methyltransferase (GNMT) and Methylenetetrahydrofolate Reductase (MTHFR).
Chiang, EP; Ko, HA; Lin, YJ; Tang, FY; Wang, YC; Wu, MT, 2015
)
0.42
" The impact of H(2)S on mitochondrial energy metabolism crucially depends on the bioavailability of this gaseous molecule and its interplay with the other two gasotransmitters."( Bioenergetic relevance of hydrogen sulfide and the interplay between gasotransmitters at human cystathionine β-synthase.
Arese, M; Forte, E; Giuffrè, A; Malagrinò, F; Sarti, P; Vicente, JB, 2016
)
0.43
" The findings will stimulate more studies on the biosynthesis of complex organoarsenicals, and lead to a better understanding of the bioavailability and function of the organoarsenicals in biological systems."( Arsenic Methyltransferase is Involved in Arsenosugar Biosynthesis by Providing DMA.
Francesconi, KA; Gao, H; Li, G; Raber, G; Rensing, C; Xue, XM; Yan, Y; Ye, J; Zhu, YG, 2017
)
0.46
"Pterostilbene, a structural analog of resveratrol, has higher oral bioavailability and bioactivity than that of the parent compound; but is far less abundant in natural sources."( De novo biosynthesis of pterostilbene in an Escherichia coli strain using a new resveratrol O-methyltransferase from Arabidopsis.
Heo, KT; Hong, YS; Kang, SY, 2017
)
0.46
"A novel, high bioavailability oral, enteric coated tablet formulation of S-adenosylmethionine (MSI-195) has been developed for life science application."( Pharmacokinetic study of a novel oral formulation of S-adenosylmethionine (MSI-195) in healthy subjects: dose escalation, food effect and comparison to a commercial nutritional supplement product.
Cameron, BR; Ferreira, L; MacDonald, ID, 2020
)
0.56
"The overall conclusion was that MSI-195 was well tolerated and has markedly higher bioavailability compared with both the SAM-e Complete™ commercial product tested and, on a per mg basis, products reported in other literature."( Pharmacokinetic study of a novel oral formulation of S-adenosylmethionine (MSI-195) in healthy subjects: dose escalation, food effect and comparison to a commercial nutritional supplement product.
Cameron, BR; Ferreira, L; MacDonald, ID, 2020
)
0.56
" In this study, solid lipid nanoparticles (SLN) were prepared in order to increase the limited oral bioavailability of SAMe, and SLN based nanocomposite particles (SAMe-SLN-NC) were further developed using an enteric polymer for passive targeting of intestinal lymphatic system."( A study to enhance the oral bioavailability of s-adenosyl-l-methionine (SAMe): SLN and SLN nanocomposite particles.
Amasya, G; Ergin, AD; Erkan Cakirci, O; Ozçelikay, AT; Sezgin Bayindir, Z; Yuksel, N, 2021
)
0.62
"40 are considered abnormal and mean that FC has a low bioavailability to the cells and so reflects a "carnitine insufficiency"."( Evaluation of carnitine nutritional status in full-term newborn infants.
Bayés, R; Campoy, C; López, C; Molina-Font, JA; Peinado, JM; Rivero, M, 1998
)
0.3
"We examined the effect of acylcarnitines on the in situ bioavailability of lucifer yellow (LY) from the loops of small and large intestines of rats."( Increases in bioavailability of poorly absorbed drug by acylcarnitine.
Doi, N; Hayashi, M; Kimura, A; Tomita, M, 2012
)
0.38
" Biotinidase has a key role in the reutilization of the biotin, catalyzing the hydrolysis of biocytin (ε-N-biotinyl-l-lysine) and biocytin-containing peptides derived from carboxylase turnover, thus contributing substantially to the bioavailability of this vitamin."( Biotinidase knockout mice show cellular energy deficit and altered carbon metabolism gene expression similar to that of nutritional biotin deprivation: clues for the pathogenesis in the human inherited disorder.
Heredia-Antúnez, A; Hernández-González, R; Hernández-Vázquez, A; Ibarra-González, I; Ortega-Cuellar, D; Pindolia, K; Velázquez-Arellano, A; Wolf, B, 2013
)
0.39
" Ketamine response resulted in more pronounced effects in the kynurenine pathway and the arginine pathway at 4 h post-infusion, where a larger decrease in circulating kynurenine levels and a larger increase in the bioavailability of arginine were observed in responders to ketamine treatment, suggesting possible mechanisms for response to ketamine treatment."( Plasma metabolomic profiling of a ketamine and placebo crossover trial of major depressive disorder and healthy control subjects.
Ferrucci, L; Gould, TD; Kadriu, B; Khadeer, M; Lovett, J; Moaddel, R; Morris, PJ; Ravichandran, S; Shardell, M; Thomas, CJ; Yuan, P; Zarate, CA, 2018
)
0.48
" Main results showed that, relative to controls, ATRA-treated mice had in plasma: increased levels of carnitine, acetylcarnitine, and longer acylcarnitine species; decreased levels of citrulline, and increased global arginine bioavailability ratio for nitric oxide synthesis; increased levels of creatine, taurine and docosahexaenoic acid; and a decreased n-6/n-3 polyunsaturated fatty acids ratio."( Novel Markers of the Metabolic Impact of Exogenous Retinoic Acid with A Focus on Acylcarnitines and Amino Acids.
Arreguín, A; Bonet, ML; Kopecky, J; Kuda, O; Palou, A; Ribot, J, 2019
)
0.51
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51
"Many studies have investigated the effects of soy isoflavones on weight control, but few have focused on the role of equol, a gut-derived metabolite of daidzein with greater bioavailability than other soy isoflavones."( Gut microbiota and acylcarnitine metabolites connect the beneficial association between equol and adiposity in adults: a prospective cohort study.
Chen, D; Chen, YM; Fu, Y; Gou, W; Jiang, Z; Liu, CY; Wu, YY; Xie, K; Yan, Y; Yang, Y; Zheng, JS; Zhu, HL, 2022
)
0.72

Dosage Studied

ExcerptRelevanceReference
"01) after 800 mg/day SAMe than after placebo while the lower dosage of SAMe did not affect UCB values."( Effect of different doses of S-adenosyl-L-methionine (SAMe) on nicotinic acid-induced hyperbilirubinaemia in Gilbert's syndrome.
Coltorti, M; Di Padova, C; Gentile, S; Le Grazie, C; Orlando, C; Persico, M, 1988
)
0.27
" In this article, data are reported on plasma kinetics, distribution, and metabolism of SAMe after oral administration since preference is given to oral dosage in the usual clinical practice."( Pharmacologic aspects of S-adenosylmethionine. Pharmacokinetics and pharmacodynamics.
Stramentinoli, G, 1987
)
0.27
"A non-controlled clinical phase IV trial was carried out involving 20,641 patients with osteoarthritis of the knee, the hip, and the spine and also with osteoarthritic polyarthritis of the fingers, who were treated with ademetionine tablets given in a fixed dosage schedule for eight weeks."( A new medical approach to the treatment of osteoarthritis. Report of an open phase IV study with ademetionine (Gumbaral).
Berger, R; Nowak, H, 1987
)
0.27
" No difference was found in comparing data in animals given SAMe at the two dosage levels."( Effect of S-adenosylmethionine on experimental osteoarthritis in rabbits.
Barceló, HA; Barreira, JC; Macias, M; Sagasta, CL; Wiemeyer, JC, 1987
)
0.27
" The extent of alkylation of liver histones was maximal at about 5h after dosing and declined between 5 and 24h."( Methylation of nuclear proteins by dimethylnitrosamine and by methionine in the rat in vivo.
Craddock, VM; Turberville, C, 1971
)
0.25
" At physiological concentrations, both hGH and oPRL have similar dose-response curves in a mouse mammary gland organ culture system."( Membrane modification differentially affects the binding of the lactogenic hormones human growth hormone and ovine prolactin.
Bhattacharya, A; Vonderhaar, BK, 1981
)
0.26
" The lowering of epinephrine concentration was greater with L-dopa than with D-dopa, was dose-related over a dosage range of 50 to 200 mg/kg of L-dopa and was not prevented by a dopamine receptor antagonist."( Effects of L-dopa on epinephrine concentration in rat brain: possible role of inhibition of norepinephrine N-methyltransferase by S-adenosylhomocysteine.
Fuller, RW; Hemrick-Luecke, SK; Perry, KW, 1982
)
0.26
" No dose-response relationship was found to exist, however."( Increased levels of S-adenosylmethionine in the livers of rats fed various forms of selenium.
Dausch, JG; Fullerton, FR, 1993
)
0.29
" To clarify the actions of SAM during different stages of ischemia/ reperfusion, we have compared its benefit in five dosage regimens, using perfused rat livers after sequential periods of 24 hr cold and 20 min rewarming ischemia."( Treatment of experimental ischemia/reperfusion injury with S-adenyosylmethionine: evidence that donor pretreatment complements other regimens.
Dunne, JB; Piratvisuth, T; Tredger, JM; Williams, R, 1997
)
0.3
" These present data clearly demonstrate that METH dosing leads to significant alterations in liver and blood SAM and that these changes in SAM levels correlate with changes in striatal dopamine levels."( Methamphetamine treatment affects blood and liver S-adenosylmethionine (SAM) in mice. Correlation with dopamine depletion in the striatum.
Ali, SF; Cooney, CA; Poirier, LA; Wise, CK, 1998
)
0.3
" Dosage suppressors of gcd10 mutations, encoding tRNAiMet (hcIMT1 to hcIMT4; hc indicates that the gene is carried on a high-copy-number plasmid) or a homologue of human La protein implicated in tRNA 3'-end formation (hcLHP1), also suppressed gcd14 mutations."( GCD14p, a repressor of GCN4 translation, cooperates with Gcd10p and Lhp1p in the maturation of initiator methionyl-tRNA in Saccharomyces cerevisiae.
Anderson, J; Calvo, O; Cuesta, R; García-Barrio, MT; Gutiérrez, N; Hinnebusch, AG; Tamame, M, 1999
)
0.3
" immediately after paracetamol overdose (T0) and 6 h after dosing (T6) and those administered S-adenosyl-L-methionine at doses of 20 mg/kg (0."( Effect of different doses of S-adenosyl-L-methionine on paracetamol hepatotoxicity in a mouse model.
Carrasco, R; Caturla, J; Esteban, A; Gutiérrez, A; Mayol, MJ; Ortiz, P; Pérez-Mateo, M, 2000
)
0.31
" B6C3F1 mice were dosed dermally with DEA (0, 10, 20, 40, 80, and 160 mg/kg) for 4 weeks (5 days/week)."( Diethanolamine induces hepatic choline deficiency in mice.
Gamsky, EA; Hicks, SM; Lehman-McKeeman, LD; Mar, MH; Vassallo, JD; Zeisel, SH, 2002
)
0.31
" One additional superimposed dosage mitigated these effects in the direction of an antidepressant profile, with the inter-drug differences waning in the 6(th) hour."( Pharmacodynamic studies on the central mode of action of S-adenosyl-L-methionine (SAMe) infusions in elderly subjects, utilizing EEG mapping and psychometry.
Anderer, P; Assandri, A; di Padova, C; Lindeck-Pozza, E; Linzmayer, L; Saletu, B; Saletu-Zyhlarz, GM; Semlitsch, HV, 2002
)
0.31
" Relevant mechanistic data provides a link between the molecular and cellular event(s) and adverse outcome, and insight into mechanism of action is critical for accurate evaluation of dose-response relationships and inter-species extrapolation."( Incorporating mechanistic data into risk assessment.
Lehman-McKeeman, LD, 2002
)
0.31
" In the 19 patients studied, there were negative correlations between dosage or absorption and extent of O-methylation and of sulfation of L-DOPA or its metabolites."( L-DOPA biotransformation: correlations of dosage, erythrocyte catechol O-methyltransferase and platelet SULT1A3 activities with metabolic pathways in Parkinsonian patients.
Decker, PA; Dousa, MK; Muenter, MD; Offord, KP; Tyce, GM; Weinshilboum, RM, 2003
)
0.32
"Subjects received oral SAMe for 4 weeks; the dosage was titrated over 5 days to 1600 mg/day."( Bioavailability and lack of toxicity of S-adenosyl-L-methionine (SAMe) in humans.
Cohen, BM; Damico, KE; Gören, JL; Sarmiento, IA; Stoll, AL, 2004
)
0.32
" A chronic longitudinal study (pre- and posttreatment parameters compared) was undertaken with 15 clinically healthy cats given a stable 1,4-butanedisulfonate (S'S isomer) SAMe salt (enteric coated tablets providing 180 mg SAMe), dosage 48 mg/kg PO q24h, on an empty stomach for 113 days."( The effects of S-adenosylmethionine on clinical pathology and redox potential in the red blood cell, liver, and bile of clinically normal cats.
Center, SA; Erb, HN; Foureman, P; Hoffmann, WE; McCabe-McClelland, J; Randolph, JF; Warner, KL,
)
0.13
" Subjects with normal MMA were randomly assigned to 1 of 3 dosage groups: 0, 25, or 100 microg cyanocobalamin/d."( Elevated serum S-adenosylhomocysteine in cobalamin-deficient elderly and response to treatment.
Allen, RH; Dolce, ET; Johnson, MA; Stabler, SP, 2006
)
0.33
" Insights to the intracellular action of sinefungin stem from the finding that increased gene dosage of yeast AdoMet synthase plus cap guanine-N7 methyltransferase afforded greater resistance to sinefungin than either enzyme alone."( Sinefungin resistance of Saccharomyces cerevisiae arising from Sam3 mutations that inactivate the AdoMet transporter or from increased expression of AdoMet synthase plus mRNA cap guanine-N7 methyltransferase.
Schwer, B; Shuman, S; Zheng, S, 2007
)
0.34
" glabrata, respectively), but showed little toxicity to mice liver cells at clinical dosage after 24 h of exposure, with the lowest lactate dehydrogenase and the highest ED(50) compared to four other azoles antifungal agents."( Antifungal activity of 25-azalanosterol against Candida species.
Wang, J; Wu, J, 2008
)
0.35
" SAM stimulated GST activity in a dose-response manner when added to homogenates derived from the above ApoE-/- mice."( S-adenosylmethionine mediates glutathione efficacy by increasing glutathione S-transferase activity: implications for S-adenosyl methionine as a neuroprotective dietary supplement.
Falcone, D; Graves, M; Shea, TB; Tchantchou, F, 2008
)
0.35
" Correcting the insufficiency by dosing folate along with the SSRI results in a significantly better antidepressant response."( The methylation, neurotransmitter, and antioxidant connections between folate and depression.
Miller, AL, 2008
)
0.35
"Randomised or quasi-randomised controlled trials that compared SAMe at any dosage and in any formulation with placebo or no intervention in patients with osteoarthritis of the knee or hip."( S-Adenosylmethionine for osteoarthritis of the knee or hip.
Jüni, P; Nüesch, E; Reichenbach, S; Rutjes, AW, 2009
)
0.35
"The objective of this study was to examine the dose-response relationship between As and global methylation of peripheral blood mononuclear cell (PBMC) DNA in apparently healthy Bangladeshi adults chronically exposed to a wide range of As concentrations in drinking water."( A dose-response study of arsenic exposure and global methylation of peripheral blood mononuclear cell DNA in Bangladeshi adults.
Alam, S; Gamble, MV; Graziano, JH; Hall, MN; Harper, KN; Ilievski, V; Levy, D; Liu, X; Mey, JL; Niedzwiecki, MM; Oka, J; Parvez, F; Siddique, AB; Slavkovich, V; van Geen, A,
)
0.13
" The assay was validated by pilot high-throughput screening (HTS), dose-response confirmation of hits, and elimination of artifacts through counterscreening against SAH detection in the absence of NSD1."( A sensitive luminescent assay for the histone methyltransferase NSD1 and other SAM-dependent enzymes.
Drake, KM; Glynn, R; Kisielewski, A; Napper, AD; Watson, VG, 2014
)
0.4
" Patients of the first group received Ademetionin in a dosage 400 mg 2 times a day within 7 days."( [Comparative results of use liver protecting drugs for prophylaxis of the liver failure after extensive resections of the liver].
Artemyev, AI; Bashkov, AN; Grigorieva, OO; Naidyonov, EV; Rudakov, VS; Voskanyan, SE; Zabezhinsky, DA; Zhurbin, AS,
)
0.13
"It was studied the influence of therapeutic and preventive administration of substances 18 and E-38 in the dosage of 12mg/kg during chronic mild stress "conflict of afferent activation" during 30 days and depression-like behavior chronic mild stress that modeled 8 weeks."( Anhedonia at experimental models of chronic stress and its correction.
Bobyriov, VM; Lutsenko, RV; Sydorenko, AH,
)
0.13
"Prolonged hyperthyroidism and hypothyroidism were modeled in experimental rats by dosing the animals with L-thyroxine and thiamazole, respectively, for 21 days."( The impact of B vitamins on the functioning of methylation cycle in the liver and the kidneys of hyper- and hypothyroid rats.
Bulko, I; Dmytrenko, I; Korda, M; Nechyporuk, V; Pentiuk, L, 2020
)
0.56
" We found that NELF-A dosage regulates Drosophila healthspan: Halving NELF-A level in the heterozygous mutants or via neuronal-specific RNAi depletion improves their locomotor activity, stress resistance, and lifespan significantly."( NELF-A controls Drosophila healthspan by regulating heat-shock protein-mediated cellular protection and heterochromatin maintenance.
Lin, WQ; Ngian, ZK; Ong, CT, 2021
)
0.62
" The current review highlights the therapeutic roles of SAMe and probiotics in depression, their mechanistic targets, and their possible synergistic effects and may help in the development of food supplements consisting of a combination of SAMe and probiotics with new dosage forms that may improve their bioavailability."( The Efficacy of S-Adenosyl Methionine and Probiotic Supplementation on Depression: A Synergistic Approach.
Daglia, M; Di Minno, A; Khan, A; Rengasamy, KRR; Sacchi, R; Ullah, H, 2022
)
0.72
" Betaine has been used for more than 30 years in pyridoxine non-responsive cystathionine beta-synthase (pnrCBS) and cobalamin C (cblC) deficiencies to lower the hyperhomocysteinemia, although little is known about the optimal therapeutic dosage and its pharmacokinetic in these patients."( Efficacy and pharmacokinetics of betaine in CBS and cblC deficiencies: a cross-over randomized controlled trial.
Alberti, C; Benoist, JF; de Baulny, HO; Feillet, F; Garcia-Segarra, N; Guilmin-Crépon, S; Haignere, J; Imbard, A; Kaguelidou, F; Kuster, A; Magréault, S; Perronneau, I; Schiff, M; Schlemmer, D; Toumazi, A, 2022
)
0.72
"Our analysis shows that there is no overt benefit to increasing betaine dosage higher than 100 mg/kg/day to lower tHcy concentrations in pnrCBS and cblC deficiencies."( Efficacy and pharmacokinetics of betaine in CBS and cblC deficiencies: a cross-over randomized controlled trial.
Alberti, C; Benoist, JF; de Baulny, HO; Feillet, F; Garcia-Segarra, N; Guilmin-Crépon, S; Haignere, J; Imbard, A; Kaguelidou, F; Kuster, A; Magréault, S; Perronneau, I; Schiff, M; Schlemmer, D; Toumazi, A, 2022
)
0.72
" Knowing the pleiotropic negative impact of Hcy on gametes, embryos and pregnancy in general, we strongly recommend a Hcy dosage in both members of couples seeking treatment for pregnancy."( The importance of preconception Hcy testing: identification of a folate trap syndrome in a woman attending an assisted reproduction program.
Clément, A; Clément, P; Menezo, YJR; Viot, G, 2023
)
0.91
" A dose-response study showed that the accumulation of long-chain acylcarnitines in serum contributes to the separation of wild-type mice undergoing APAP-induced hepatotoxicity from other mouse groups in a multivariate model."( Serum metabolomics reveals irreversible inhibition of fatty acid beta-oxidation through the suppression of PPARalpha activation as a contributing mechanism of acetaminophen-induced hepatotoxicity.
Chen, C; Gonzalez, FJ; Idle, JR; Krausz, KW; Shah, YM, 2009
)
0.35
" In a double blind 2 × 2 Latin square design at a dosage of 100 mg/kg body weight (BW)/day for 28 days the effects of oral supplementation of L-carnitine (as fumarate) were assessed."( The effect of long-term oral L-carnitine administration on insulin sensitivity, glucose disposal, plasma concentrations of leptin and acylcarnitines, and urinary acylcarnitine excretion in warmblood horses.
Buyse, J; de Graaf-Roelfsema, E; de Sain-van der Velden, MG; Janssens, GP; Kranenburg, LC; van den Broek, J; van der Kolk, JH; Westermann, CM, 2014
)
0.4
"The current study supports the treatment rationale of short-chain acyl-CoA dehydrogenase deficiency in humans with L-carnitine at an oral dosage of 100 mg/kg BW/day."( The effect of long-term oral L-carnitine administration on insulin sensitivity, glucose disposal, plasma concentrations of leptin and acylcarnitines, and urinary acylcarnitine excretion in warmblood horses.
Buyse, J; de Graaf-Roelfsema, E; de Sain-van der Velden, MG; Janssens, GP; Kranenburg, LC; van den Broek, J; van der Kolk, JH; Westermann, CM, 2014
)
0.4
" Time-related changes in the serum and muscle ACC profiles were demonstrated that were not affected by the CLA supplement at the dosage used in the present study."( Acylcarnitine profiles in serum and muscle of dairy cows receiving conjugated linoleic acids or a control fat supplement during early lactation.
Adamski, J; Dänicke, S; Prehn, C; Rehage, J; Sadri, H; Saremi, B; Sauerwein, H; Yang, Y, 2019
)
0.51
" In brief, a total of 148 Sprague-Dawley rats (offspring) were dosed with estradiol benzoate (EB) on postnatal days (PNDs) 1, 3 and 5, and subsequently dosed with testosterone (T)/estradiol (E) tubes via subcutaneous implants from PND 90 to 200."( Distinct lipid signatures are identified in the plasma of rats with chronic inflammation induced by estradiol benzoate and sex hormones.
Beger, RD; Cao, Z; Nakamura, N; Pence, LM, 2020
)
0.56
"Our goal was to determine the efficacy of the American Society for Parenteral and Enteral Nutrition's recommended carnitine dosage of 5 mg/kg/day in maintaining normal serum free carnitine and total acylcarnitine levels in preterm neonates receiving parenteral nutrition (PN)."( Carnitine supplementation increases serum concentrations of free carnitine and total acylcarnitine in preterm neonates: A retrospective cohort study.
Miller, M; Morrissey, M; Rastogi, D; Rastogi, S; Sasenick, J, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (7)

RoleDescription
cofactorAn organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
coenzymeA low-molecular-weight, non-protein organic compound participating in enzymatic reactions as dissociable acceptor or donor of chemical groups or electrons.
nutraceuticalA product in capsule, tablet or liquid form that provide essential nutrients, such as a vitamin, an essential mineral, a protein, an herb, or similar nutritional substance.
micronutrientAny nutrient required in small quantities by organisms throughout their life in order to orchestrate a range of physiological functions.
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
Mycoplasma genitalium metaboliteAny bacterial metabolite produced during a metabolic reaction in Mycoplasma genitalium.
cofactorAn organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (3)

ClassDescription
sulfonium compound
organic cationAny organic ion with a net positive charge.
sulfonium compound
sulfonium betaineNeutral molecules having charge-separated forms with an sulfonium atom which bears no hydrogen atoms and that is not adjacent to the anionic atom.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (1,748)

PathwayProteinsCompounds
Transport of small molecules39295
SLC-mediated transmembrane transport13567
Transport of inorganic cations/anions and amino acids/oligopeptides5427
Developmental Biology72730
Reproduction868
Meiosis594
Meiotic recombination292
Metabolism14961108
Metabolism of lipids500463
Phospholipid metabolism12242
Glycerophospholipid biosynthesis7439
Synthesis of PC2017
Metabolism of vitamins and cofactors146155
Metabolism of water-soluble vitamins and cofactors102114
Cobalamin (Cbl, vitamin B12) transport and metabolism1825
Nicotinate metabolism2243
Nicotinamide salvaging1030
Molybdenum cofactor biosynthesis817
Amino acid and derivative metabolism250260
Histidine catabolism822
Metabolism of polyamines5621
Creatine metabolism615
Metabolism of amine-derived hormones1440
Catecholamine biosynthesis418
Serotonin and melatonin biosynthesis315
Glyoxylate metabolism and glycine degradation2037
Sulfur amino acid metabolism2763
Selenoamino acid metabolism2450
Metabolism of ingested SeMet, Sec, MeSec into H2Se423
Methylation of MeSeH for excretion15
Formation of selenosugars for excretion011
Biological oxidations150276
Phase II - Conjugation of compounds73122
Methylation1338
DNA Repair25547
DNA Double-Strand Break Repair10313
DNA Double Strand Break Response379
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks337
Signaling Pathways1269117
Visual phototransduction6241
The phototransduction cascade2621
Inactivation, recovery and regulation of the phototransduction cascade2518
Signaling by WNT14820
TCF dependent signaling in response to WNT1049
Formation of the beta-catenin:TCF transactivating complex224
MAPK family signaling cascades11519
ERK1/ERK2 pathway9319
RAF/MAP kinase cascade9119
Cellular responses to stimuli48356
Cellular responses to stress46954
Cellular Senescence849
Oxidative Stress Induced Senescence257
Senescence-Associated Secretory Phenotype (SASP)374
Neuronal System16650
Transmission across Chemical Synapses12250
Neurotransmitter clearance725
Clearance of dopamine413
Enzymatic degradation of dopamine by COMT310
Enzymatic degradation of Dopamine by monoamine oxidase210
Cell Cycle53831
Cell Cycle, Mitotic41031
Mitotic G2-G2/M phases1738
G2/M Transition1728
Cyclin A/B1/B2 associated events during G2/M transition187
M Phase27921
Mitotic Prophase6214
Condensation of Prophase Chromosomes1310
Histidine Metabolism1735
Nicotinate and Nicotinamide Metabolism1434
Glycine and Serine Metabolism2452
Arginine and Proline Metabolism2047
Tryptophan Metabolism1855
Tyrosine Metabolism1657
Betaine Metabolism818
Carnitine Synthesis517
Catecholamine Biosynthesis314
Methionine Metabolism1637
Spermidine and Spermine Biosynthesis614
Ubiquinone Biosynthesis518
Prolidase Deficiency (PD)2047
Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)2047
Hyperprolinemia Type II2047
Hyperprolinemia Type I2047
Prolinemia Type II2047
Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)2047
Ornithine Aminotransferase Deficiency (OAT Deficiency)2047
Aromatic L-Aminoacid Decarboxylase Deficiency314
Cystathionine beta-Synthase Deficiency1637
Hypermethioninemia1637
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency1637
Glycine N-Methyltransferase Deficiency1637
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)1637
Methionine Adenosyltransferase Deficiency1637
Histidinemia1735
Alkaptonuria1657
Hawkinsinuria1657
Tyrosinemia Type I1657
Dimethylglycine Dehydrogenase Deficiency2452
Dihydropyrimidine Dehydrogenase Deficiency (DHPD)2452
Sarcosinemia2452
Non-Ketotic Hyperglycinemia2452
Azathioprine Action Pathway4782
Mercaptopurine Action Pathway4780
Phenytoin (Antiarrhythmic) Action Pathway6923
Thioguanine Action Pathway4781
Disulfiram Action Pathway2366
Hyperglycinemia, Non-Ketotic2452
Tyrosinemia, Transient, of the Newborn1657
Tyrosine Hydroxylase Deficiency314
Dopamine beta-Hydroxylase Deficiency1657
Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency2047
Hyperornithinemia with Gyrate Atrophy (HOGA)2047
Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]2047
L-Arginine:Glycine Amidinotransferase Deficiency2047
Monoamine Oxidase-A Deficiency (MAO-A)1657
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type1637
Mercaptopurine Metabolism Pathway1524
Methylhistidine Metabolism14
3-Phosphoglycerate Dehydrogenase Deficiency2452
Lipoic Acid Metabolism310
Tyrosine Biosynthesis519
Quorum Sensing1020
S-Adenosyl-L-Methionine Biosynthesis817
Secondary Metabolites: Ubiquinol Biosynthesis922
Metabolism of proteins1058144
Translation26733
PreQ0 Metabolism623
Menaquinol Biosythesis1224
Thiamin Diphosphate Biosynthesis1027
Secondary Metabolites: Ubiquinol Biosynthesis 2923
Spermidine Biosynthesis I611
Thiazole Biosynthesis I314
S-Adenosyl-L-Methionine Cycle414
Spermidine Biosynthesis and Metabolism39
Lipoate Biosynthesis and Incorporation I24
Cyclopropane Fatty Acid (CFA) Biosynthesis13
Operon: Methionine Biosynthesis Inactivation11
Methionine Metabolism and Salvage1534
Sarcosine Oncometabolite Pathway1321
Lysolipid Incorporation into Mitochondria514
Lysolipid Incorporation into ER1023
Cholesterol biosynthesis and metabolism CE(14:0)2250
Cholesterol biosynthesis and metabolism CE(10:0)2250
Cholesterol Biosynthesis and Metabolism CE(12:0)2250
Cholesterol Biosynthesis and Metabolism CE(16:0)2250
Cholesterol biosynthesis and metabolism CE(18:0)2250
Lysolipid incorporation into Mitochondria PC(16:0/16:0)515
Lysolipid Incorporation into ER PC(10:0/10:0)1016
Lysolipid Incorporation into ER PC(14:0/14:0)1023
Lysolipid Incorporation into ER PC(16:0/16:0)1024
Lysolipid Incorporation into ER PC(16:1(9Z)/16:1(9Z))1024
Lysolipid Incorporation into ER PC(16:1(11Z)/16:1(11Z))1017
Lysolipid Incorporation into ER PC(18:0/18:0)1024
Lysolipid Incorporation into ER PC(18:1(9Z)/18:1(9Z))1023
Lysolipid Incorporation into ER PC(18:2(9Z,11Z)/18:2(9Z,11Z))1019
Lysolipid Incorporation into ER PC(20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z))1023
Lysolipid incorporation into Mitochondria PC(10:0/10:0)58
Lysolipid incorporation into Mitochondria PC(14:0/14:0)514
Lysolipid incorporation into Mitochondria PC(16:1(9Z)/16:1(9Z))515
Lysolipid incorporation into Mitochondria PC(16:1(11Z)/16:1(11Z))59
Lysolipid incorporation into Mitochondria PC(18:0/18:0)515
Lysolipid incorporation into Mitochondria PC(18:1(9Z)/18:1(9Z))514
Lysolipid incorporation into Mitochondria PC(18:2(9Z,11Z)/18:2(9Z,11Z))510
Lysolipid incorporation into Mitochondria PC(20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z))514
Phosphatidylcholine biosynthesis PC(10:0/10:0)23
Phosphatidylcholine biosynthesis PC(10:0/12:0)23
Phosphatidylcholine biosynthesis PC(10:0/14:0)23
Phosphatidylcholine biosynthesis PC(10:0/15:0)23
Phosphatidylcholine biosynthesis PC(10:0/16:0)23
Phosphatidylcholine biosynthesis PC(12:0/12:0)23
Phosphatidylcholine biosynthesis PC(12:0/14:0)23
Phosphatidylcholine biosynthesis PC(12:0/15:0)23
Phosphatidylcholine biosynthesis PC(12:0/16:0)23
Phosphatidylcholine biosynthesis PC(14:0/15:0)27
Phosphatidylcholine biosynthesis PC(10:0/14:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/14:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/14:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/14:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:0/14:1(9Z))27
Phosphatidylcholine biosynthesis PC(14:0/14:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/15:0)27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/15:0)23
Phosphatidylcholine biosynthesis PC(15:0/15:0)27
Phosphatidylcholine biosynthesis PC(10:0/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(10:0/20:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/16:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/18:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/18:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:0/16:1(9Z))27
Phosphatidylcholine biosynthesis PC(14:0/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:0/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:0/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/16:0)27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/16:0)23
Phosphatidylcholine biosynthesis PC(15:0/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:0/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/16:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/14:1(9Z))27
Phosphatidylcholine biosynthesis PC(14:1(9Z)/14:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/14:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/14:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/16:1(9Z))27
Phosphatidylcholine biosynthesis PC(14:1(9Z)/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/16:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/15:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/15:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/16:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/16:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:0/16:0)27
Phosphatidylcholine biosynthesis PC(15:0/16:1(9Z))27
Phosphatidylcholine biosynthesis PC(15:0/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/16:0)23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/16:0)23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(14:1(9Z)/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/18:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/18:1(11Z))23
Phosphatidylcholine biosynthesis PC(16:1(9Z)/16:1(9Z))27
Phosphatidylcholine biosynthesis PC(16:1(9Z)/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(16:1(11Z)/16:1(9Z))23
Phosphatidylcholine biosynthesis PC(16:1(11Z)/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/18:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/18:1(11Z))23
Phosphatidylcholine biosynthesis PC(16:0/16:1(9Z))27
Phosphatidylcholine biosynthesis PC(16:0/16:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/22:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/22:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/18:0)23
Phosphatidylcholine biosynthesis PC(12:0/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(12:0/20:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:0/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(14:0/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(14:1(9Z)/18:0)27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/18:0)23
Phosphatidylcholine biosynthesis PC(16:0/16:0)27
Phosphatidylcholine biosynthesis PC(15:1(9Z)/18:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/18:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/18:1(9Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/18:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/23:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/23:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/18:0)23
Phosphatidylcholine biosynthesis PC(15:0/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(15:0/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(15:1(9Z)/18:0)23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/18:0)23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/20:1(11Z))27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/20:1(11Z))23
Phosphatidylcholine biosynthesis PC(16:1(9Z)/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(16:1(9Z)/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(16:1(11Z)/18:1(9Z))23
Phosphatidylcholine biosynthesis PC(16:1(11Z)/18:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/24:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/24:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/22:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/22:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:0/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(14:0/20:1(11Z))27
Phosphatidylcholine biosynthesis PC(14:0/18:0)27
Phosphatidylcholine biosynthesis PC(14:1(9Z)/20:0)27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/20:0)23
Phosphatidylcholine biosynthesis PC(16:0/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(16:0/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(16:1(9Z)/18:0)27
Phosphatidylcholine biosynthesis PC(16:1(11Z)/18:0)23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(15:1(9Z)/20:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/20:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/25:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/25:1(11Z))23
Phosphatidylcholine biosynthesis PC(10:0/20:0)23
Phosphatidylcholine biosynthesis PC(12:0/23:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/23:1(11Z))23
Phosphatidylcholine biosynthesis PC(15:0/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(15:0/20:1(11Z))27
Phosphatidylcholine biosynthesis PC(15:0/16:0)27
Phosphatidylcholine biosynthesis PC(15:1(9Z)/20:0)23
Phosphatidylcholine biosynthesis PC(15:1(11Z)/20:0)23
Phosphatidylcholine biosynthesis PC(16:0/18:0)27
Phosphatidylcholine biosynthesis PC(14:1(9Z)/22:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/22:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/22:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:1(11Z)/22:1(11Z))23
Phosphatidylcholine biosynthesis PC(16:1(9Z)/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(16:1(9Z)/20:1(11Z))27
Phosphatidylcholine biosynthesis PC(16:1(11Z)/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(16:1(11Z)/20:1(11Z))23
Phosphatidylcholine biosynthesis PC(18:1(9Z)/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(18:1(9Z)/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(18:1(11Z)/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(18:1(11Z)/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(18:0/18:1(9Z))27
Phosphatidylcholine biosynthesis PC(18:0/18:1(11Z))27
Phosphatidylcholine biosynthesis PC(10:0/26:1(9Z))23
Phosphatidylcholine biosynthesis PC(10:0/26:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/24:1(9Z))23
Phosphatidylcholine biosynthesis PC(12:0/24:1(11Z))23
Phosphatidylcholine biosynthesis PC(12:0/20:0)23
Phosphatidylcholine biosynthesis PC(14:0/22:1(9Z))23
Phosphatidylcholine biosynthesis PC(14:0/22:1(11Z))23
Phosphatidylcholine biosynthesis PC(14:1(9Z)/22:0)27
Phosphatidylcholine biosynthesis PC(14:1(11Z)/22:0)23
Phosphatidylcholine biosynthesis PC(16:0/20:1(13Z))23
Phosphatidylcholine biosynthesis PC(16:0/20:1(11Z))27
Phosphatidylcholine biosynthesis PC(16:1(9Z)/20:0)27
Phosphatidylcholine biosynthesis PC(16:1(11Z)/20:0)23
Phosphatidylcholine biosynthesis PC(18:0/18:0)27
Eukaryotic Translation Termination45
Post-translational protein modification666112
Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation4626
Synthesis of diphthamide-EEF287
Protein methylation174
Molybdenum Cofactor Biosynthesis615
Flavonoid Biosynthesis1150
Flavone and Flavonol Biosynthesis627
Choline Biosynthesis I415
Choline Biosynthesis II618
Phylloquinol Biosynthesis516
Plastoquinol-9 Biosynthesis616
Thio-Molybdenum Cofactor Biosynthesis717
Glycine Betaine Biosynthesis I621
Glycine Betaine Biosynthesis II824
Protein repair39
Phosphatidylcholine Biosynthesis615
Phosphatidylcholine Biosynthesis PC(14:0/14:0)620
Phosphatidylcholine Biosynthesis PC(14:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(14:0/15:0)620
Phosphatidylcholine Biosynthesis PC(14:0/16:0)620
Phosphatidylcholine Biosynthesis PC(14:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(14:0/18:0)620
Phosphatidylcholine Biosynthesis PC(14:0/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(14:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(14:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(14:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(14:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(14:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:0)620
Phosphatidylcholine Biosynthesis PC(14:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(14:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(14:0/22:0)620
Phosphatidylcholine Biosynthesis PC(14:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(14:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(14:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(14:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(14:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(14:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(14:0/24:0)620
Phosphatidylcholine Biosynthesis PC(14:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(15:0/14:0)620
Phosphatidylcholine Biosynthesis PC(15:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(15:0/15:0)620
Phosphatidylcholine Biosynthesis PC(15:0/16:0)620
Phosphatidylcholine Biosynthesis PC(15:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(15:0/18:0)620
Phosphatidylcholine Biosynthesis PC(15:0/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(15:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(15:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(15:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(15:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(15:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:0)620
Phosphatidylcholine Biosynthesis PC(15:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(15:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(15:0/22:0)620
Phosphatidylcholine Biosynthesis PC(15:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(15:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(15:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(15:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(15:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(15:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(15:0/24:0)620
Phosphatidylcholine Biosynthesis PC(15:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(16:0/14:0)620
Phosphatidylcholine Biosynthesis PC(16:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(16:0/15:0)620
Phosphatidylcholine Biosynthesis PC(16:0/16:0)620
Phosphatidylcholine Biosynthesis PC(16:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(16:0/18:0)620
Phosphatidylcholine Biosynthesis PC(16:0/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(16:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(16:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(16:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(16:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(16:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:0)620
Phosphatidylcholine Biosynthesis PC(16:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(16:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(16:0/22:0)620
Phosphatidylcholine Biosynthesis PC(16:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(16:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(16:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(16:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(16:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(16:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(16:0/24:0)620
Phosphatidylcholine Biosynthesis PC(16:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(16:1(9Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:0/14:0)620
Phosphatidylcholine Biosynthesis PC(18:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:0/15:0)620
Phosphatidylcholine Biosynthesis PC(18:0/16:0)620
Phosphatidylcholine Biosynthesis PC(18:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:0/18:0)620
Phosphatidylcholine Biosynthesis PC(18:0/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:0)620
Phosphatidylcholine Biosynthesis PC(18:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:0/22:0)620
Phosphatidylcholine Biosynthesis PC(18:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:0/24:0)620
Phosphatidylcholine Biosynthesis PC(18:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(18:4(6Z,9Z,12Z,15Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:0/14:0)620
Phosphatidylcholine Biosynthesis PC(20:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:0/15:0)620
Phosphatidylcholine Biosynthesis PC(20:0/16:0)620
Phosphatidylcholine Biosynthesis PC(20:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:0/18:0)620
Phosphatidylcholine Biosynthesis PC(20:0/18:1(11Z))620
Disease1278231
Phosphatidylcholine Biosynthesis PC(20:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:0)620
Phosphatidylcholine Biosynthesis PC(20:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:0/22:0)620
Phosphatidylcholine Biosynthesis PC(20:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:0/24:0)620
Phosphatidylcholine Biosynthesis PC(20:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:2(11Z,14Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:3(5Z,8Z,11Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:3(8Z,11Z,14Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:4(5Z,8Z,11Z,14Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:4(8Z,11Z,14Z,17Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(20:5(5Z,8Z,11Z,14Z,17Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:0/14:0)620
Phosphatidylcholine Biosynthesis PC(22:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:0/15:0)620
Phosphatidylcholine Biosynthesis PC(22:0/16:0)620
Phosphatidylcholine Biosynthesis PC(22:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:0/18:0)620
Phosphatidylcholine Biosynthesis PC(22:0/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:0)620
Phosphatidylcholine Biosynthesis PC(22:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:0/22:0)620
Phosphatidylcholine Biosynthesis PC(22:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:0/24:0)620
Phosphatidylcholine Biosynthesis PC(22:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(22:1(13Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(22:2(13Z,16Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(22:5(4Z,7Z,10Z,13Z,16Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(22:5(7Z,10Z,13Z,16Z,19Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(22:6(4Z,7Z,10Z,13Z,16Z,19Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(24:0/14:0)620
Phosphatidylcholine Biosynthesis PC(24:0/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(24:0/15:0)620
Phosphatidylcholine Biosynthesis PC(24:0/16:0)620
Phosphatidylcholine Biosynthesis PC(24:0/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(24:0/18:0)620
Phosphatidylcholine Biosynthesis PC(24:0/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(24:0/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(24:0/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(24:0/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(24:0/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(24:0/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:0)620
Phosphatidylcholine Biosynthesis PC(24:0/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(24:0/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(24:0/22:0)620
Phosphatidylcholine Biosynthesis PC(24:0/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(24:0/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(24:0/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(24:0/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(24:0/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(24:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(24:0/24:0)620
Phosphatidylcholine Biosynthesis PC(24:0/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/14:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/14:1(9Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/15:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/16:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/16:1(9Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:1(11Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:1(9Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:2(9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:3(6Z,9Z,12Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:3(9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/18:4(6Z,9Z,12Z,15Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:1(11Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:2(11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:3(5Z,8Z,11Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:3(8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:4(5Z,8Z,11Z,14Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:4(8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/20:5(5Z,8Z,11Z,14Z,17Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:1(13Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:2(13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:4(7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:5(4Z,7Z,10Z,13Z,16Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:5(7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/24:0)620
Phosphatidylcholine Biosynthesis PC(24:1(15Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/24:1(15Z))620
Phosphatidylcholine Biosynthesis PC(11D3/11D3)620
Phosphatidylcholine Biosynthesis PC(11D3/11D5)620
Phosphatidylcholine Biosynthesis PC(11D3/13D5)620
Phosphatidylcholine Biosynthesis PC(11D3/9D3)620
Phosphatidylcholine Biosynthesis PC(11D3/9D5)620
Phosphatidylcholine Biosynthesis PC(11D3/11M3)620
Phosphatidylcholine Biosynthesis PC(11D3/11M5)620
Phosphatidylcholine Biosynthesis PC(11D3/13M5)620
Phosphatidylcholine Biosynthesis PC(11D3/9M5)620
Phosphatidylcholine Biosynthesis PC(11D5/11D3)620
Phosphatidylcholine Biosynthesis PC(11D5/11D5)620
Phosphatidylcholine Biosynthesis PC(11D5/13D5)620
Phosphatidylcholine Biosynthesis PC(11D5/9D3)620
Phosphatidylcholine Biosynthesis PC(11D5/9D5)620
Phosphatidylcholine Biosynthesis PC(11D5/11M3)620
Phosphatidylcholine Biosynthesis PC(11D5/11M5)620
Phosphatidylcholine Biosynthesis PC(11D5/13M5)620
Phosphatidylcholine Biosynthesis PC(11D5/9M5)620
Phosphatidylcholine Biosynthesis PC(13D5/11D3)620
Phosphatidylcholine Biosynthesis PC(13D5/11D5)620
Phosphatidylcholine Biosynthesis PC(13D5/13D5)620
Phosphatidylcholine Biosynthesis PC(13D5/9D3)620
Phosphatidylcholine Biosynthesis PC(13D5/9D5)620
Phosphatidylcholine Biosynthesis PC(13D5/11M3)620
Phosphatidylcholine Biosynthesis PC(13D5/11M5)620
Phosphatidylcholine Biosynthesis PC(13D5/13M5)620
Phosphatidylcholine Biosynthesis PC(13D5/9M5)620
Phosphatidylcholine Biosynthesis PC(9D3/11D3)620
Phosphatidylcholine Biosynthesis PC(9D3/11D5)620
Phosphatidylcholine Biosynthesis PC(9D3/13D5)620
Phosphatidylcholine Biosynthesis PC(9D3/9D3)620
Phosphatidylcholine Biosynthesis PC(9D3/9D5)620
Phosphatidylcholine Biosynthesis PC(9D3/11M3)620
Phosphatidylcholine Biosynthesis PC(9D3/11M5)620
Phosphatidylcholine Biosynthesis PC(9D3/13M5)620
Phosphatidylcholine Biosynthesis PC(9D3/9M5)620
Phosphatidylcholine Biosynthesis PC(9D5/11D3)620
Phosphatidylcholine Biosynthesis PC(9D5/11D5)620
Phosphatidylcholine Biosynthesis PC(9D5/13D5)620
Phosphatidylcholine Biosynthesis PC(9D5/9D3)620
Phosphatidylcholine Biosynthesis PC(9D5/9D5)620
Phosphatidylcholine Biosynthesis PC(9D5/11M3)620
Phosphatidylcholine Biosynthesis PC(9D5/11M5)620
Phosphatidylcholine Biosynthesis PC(9D5/13M5)620
Phosphatidylcholine Biosynthesis PC(9D5/9M5)620
Phosphatidylcholine Biosynthesis PC(11M3/11D3)620
Phosphatidylcholine Biosynthesis PC(11M3/11D5)620
Phosphatidylcholine Biosynthesis PC(11M3/13D5)620
Phosphatidylcholine Biosynthesis PC(11M3/9D3)620
Phosphatidylcholine Biosynthesis PC(11M3/9D5)620
Phosphatidylcholine Biosynthesis PC(11M3/11M3)620
Phosphatidylcholine Biosynthesis PC(11M3/11M5)620
Phosphatidylcholine Biosynthesis PC(11M3/13M5)620
Phosphatidylcholine Biosynthesis PC(11M3/9M5)620
Phosphatidylcholine Biosynthesis PC(11M5/11D3)620
Phosphatidylcholine Biosynthesis PC(11M5/11D5)620
Phosphatidylcholine Biosynthesis PC(11M5/13D5)620
Phosphatidylcholine Biosynthesis PC(11M5/9D3)620
Phosphatidylcholine Biosynthesis PC(11M5/9D5)620
Phosphatidylcholine Biosynthesis PC(11M5/11M3)620
Phosphatidylcholine Biosynthesis PC(11M5/11M5)620
Phosphatidylcholine Biosynthesis PC(11M5/13M5)620
Phosphatidylcholine Biosynthesis PC(11M5/9M5)620
Phosphatidylcholine Biosynthesis PC(13M5/11D3)620
Phosphatidylcholine Biosynthesis PC(13M5/11D5)620
Phosphatidylcholine Biosynthesis PC(13M5/13D5)620
Phosphatidylcholine Biosynthesis PC(13M5/9D3)620
Phosphatidylcholine Biosynthesis PC(13M5/9D5)619
Phosphatidylcholine Biosynthesis PC(13M5/11M3)620
Phosphatidylcholine Biosynthesis PC(13M5/11M5)620
Phosphatidylcholine Biosynthesis PC(13M5/13M5)620
Phosphatidylcholine Biosynthesis PC(13M5/9M5)620
Phosphatidylcholine Biosynthesis PC(9M5/11D3)619
Phosphatidylcholine Biosynthesis PC(9M5/11D5)620
Phosphatidylcholine Biosynthesis PC(9M5/13D5)620
Phosphatidylcholine Biosynthesis PC(9M5/9D3)620
Phosphatidylcholine Biosynthesis PC(9M5/9D5)620
Phosphatidylcholine Biosynthesis PC(9M5/11M3)620
Phosphatidylcholine Biosynthesis PC(9M5/11M5)620
Phosphatidylcholine Biosynthesis PC(9M5/13M5)620
Phosphatidylcholine Biosynthesis PC(9M5/9M5)620
Estrone Metabolism1622
Diseases of metabolism69121
Defects in vitamin and cofactor metabolism1717
Defects in cobalamin (B12) metabolism1114
Defective MTRR causes HMAE16
Metabolic disorders of biological oxidation enzymes647
Defective TPMT causes TPMT deficiency02
Stilbenoid, Diarylheptanoid, and Gingerol Biosynthesis417
Phosphatidylcholine Biosynthesis PC(16:0/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(18:0/20:1(13Z))1120
Chromatin organization12016
Phosphatidylcholine Biosynthesis PC(18:1(9Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(18:1(11Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(18:2(9Z,12Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(18:3(6Z,9Z,12Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(18:3(9Z,12Z,15Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(20:0/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(20:1(11Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(20:1(13Z)/20:1(13Z))1120
Phosphatidylcholine Biosynthesis PC(20:1(13Z)/22:0)1120
Phosphatidylcholine Biosynthesis PC(20:1(13Z)/22:1(13Z))1120
Chromatin modifying enzymes12016
PKMTs methylate histone lysines142
RMTs methylate histone arginines184
Gene expression (Transcription)90249
RNA Polymerase II Transcription72842
Generic Transcription Pathway60839
Transcriptional Regulation by TP5321931
Regulation of TP53 Activity9910
Regulation of TP53 Activity through Methylation154
Spermine Syn07
Transcriptional regulation by RUNX11216
S-adenosyl-L-methionine salvage II011
ethene biosynthesis I (plants)015
RUNX1 regulates transcription of genes involved in differentiation of HSCs604
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis I011
diphthamide biosynthesis II (eukaryotes)013
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function222
pyocyanin biosynthesis011
superpathway of proto- and siroheme biosynthesis1638
phosphatidylcholine biosynthesis V14
superpathway of phosphatidylcholine biosynthesis818
simple coumarins biosynthesis2221
cyclopropane fatty acid (CFA) biosynthesis23
Gene Silencing by RNA765
MicroRNA (miRNA) biogenesis205
PIWI-interacting RNA (piRNA) biogenesis292
Epigenetic regulation of gene expression11717
PRC2 methylates histones and DNA92
Positive epigenetic regulation of rRNA expression404
Activation of rRNA Expression by ERCC6 (CSB) and EHMT2 (G9a)102
Negative epigenetic regulation of rRNA expression456
SIRT1 negatively regulates rRNA expression95
NoRC negatively regulates rRNA expression423
DNA methylation62
diphthamide biosynthesis I (archaea)011
Metabolism of RNA63740
mRNA Capping156
rRNA processing18610
rRNA processing in the nucleus and cytosol1768
rRNA modification in the nucleus and cytosol588
tRNA processing10729
tRNA modification in the nucleus and cytosol4325
Synthesis of wybutosine at G37 of tRNA(Phe)616
Non-coding RNA Metabolism522
snRNP Assembly522
spermidine hydroxycinnamic acid conjugates biosynthesis414
choline biosynthesis I221
vestitol and sativan biosynthesis08
aucuparin biosynthesis612
u03B2-alanine betaine biosynthesis16
L-nicotianamine biosynthesis94
caffeine biosynthesis II (via paraxanthine)011
superpathway of plastoquinol biosynthesis318
phenylpropanoids methylation (ice plant)125
polymethylated quercetin biosynthesis210
methyl indole-3-acetate interconversion212
yatein biosynthesis II19
u03B3-coniciene and coniine biosynthesis012
free phenylpropanoid acid biosynthesis410
dimethylsulfoniopropanoate biosynthesis I (Wollastonia)115
nevadensin biosynthesis012
superpathway of thiamine diphosphate biosynthesis III (eukaryotes)324
isoflavonoid biosynthesis II124
simplecoumarins biosynthesis620
ephedrine biosynthesis019
choline biosynthesis II08
superpathway of choline biosynthesis1122
N-methyl-u03941-pyrrolinium cation biosynthesis021
chelerythrine biosynthesis1024
gossypetin metabolism025
chrysoeriol biosynthesis05
superpathway of seleno-compound metabolism339
polymethylated myricetin biosynthesis (tomato)27
spermine biosynthesis07
L-methionine degradation I (to L-homocysteine)211
sakuranetin biosynthesis012
echinatin biosynthesis010
superpathway of phylloquinol biosynthesis1731
L-methionine salvage cycle II (plants)829
seleno-amino acid detoxification and volatilization I14
pterostilbene biosynthesis16
vitexin and derivatives biosynthesis015
diacylglyceryl-N,N,N-trimethylhomoserine biosynthesis14
vitamin E biosynthesis (tocopherols)017
phosphatidylcholine biosynthesis IV211
hesperitin glycoside biosynthesis010
laudanine biosynthesis07
(S)-reticuline biosynthesis I030
furaneol and mesifurane biosynthesis214
sorgoleone biosynthesis517
volatile benzenoid biosynthesis I (ester formation)119
seleno-amino acid detoxification and volatilization II011
26,27-dehydrozymosterol metabolism15
suberin monomers biosynthesis1036
chlorogenic acid biosynthesis I615
DIMBOA-glucoside biosynthesis210
juvenile hormone III biosynthesis I017
L-methionine salvage cycle I (bacteria and plants)232
N-methylanthraniloyl-u03B2-D-glucopyranose biosynthesis37
methylquercetin biosynthesis29
eupatolitin 3-O-glucoside biosynthesis030
betaxanthin biosynthesis09
superpathway of pterocarpan biosynthesis (via formononetin)031
pinitol biosynthesis II016
superpathway of avenacin A biosynthesis615
ergosterol biosynthesis II113
S-methyl-L-methionine cycle36
sulfur volatiles biosynthesis26
S-adenosyl-L-methionine cycle II427
serotonin and melatonin biosynthesis014
salvigenin biosynthesis713
3,5-dimethoxytoluene biosynthesis46
palmatine biosynthesis016
papaverine biosynthesis312
polymethylated quercetin glucoside biosynthesis I - quercetin series (Chrysosplenium)226
coniferyl alcohol 9-methyl ester biosynthesis28
glutathione-mediated detoxification II816
ajmaline and sarpagine biosynthesis137
phosphatidylcholine biosynthesis II512
superpathway of hyoscyamine and scopolamine biosynthesis434
7-dehydroporiferasterol biosynthesis08
2'-deoxymugineic acid phytosiderophore biosynthesis1115
yatein biosynthesis I010
daphnetin modification111
phylloquinol biosynthesis213
superpathway of polyamine biosynthesis012
theobromine biosynthesis I09
polymethylated kaempferol biosynthesis18
t-anethole biosynthesis29
scopoletin biosynthesis411
superpathway of phospholipid biosynthesis II (plants)1731
methylhalides biosynthesis (plants)28
caffeine biosynthesis I011
gramine biosynthesis07
coumarins biosynthesis (engineered)628
6-methoxypodophyllotoxin biosynthesis014
syringetin biosynthesis214
superpathway of polyamine biosynthesis II114
pinitol biosynthesis I16
superpathway of benzoxazinoid glucosides biosynthesis920
dimethylsulfoniopropanoate biosynthesis II (Spartina)021
theobromine biosynthesis II (via xanthine)06
6-gingerol biosynthesis04
botryococcenes and methylated squalene biosynthesis014
sterculate biosynthesis05
xanthohumol biosynthesis216
molybdenum cofactor biosynthesis618
phenylpropanoid biosynthesis1628
S-adenosyl-L-methionine biosynthesis16
isoflavonoid biosynthesis I014
superpathway of betalain biosynthesis241
1,3,5-trimethoxybenzene biosynthesis57
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)1221
vitamin E biosynthesis (tocotrienols)113
ferulate and sinapate biosynthesis013
pinosylvin metabolism211
superpathway of nicotine biosynthesis229
gibberellin inactivation II (methylation)010
tricetin methylation16
acacetin biosynthesis05
sanguinarine and macarpine biosynthesis639
trigonelline biosynthesis06
homogalacturonan biosynthesis015
siroheme biosynthesis111
gossypol biosynthesis021
phosphatidylcholine biosynthesis III210
polymethylated quercetin glucoside biosynthesis II - quercetagetin series (Chrysosplenium)231
pinobanksin biosynthesis115
superpathway of flavones and derivatives biosynthesis1744
kaempferide triglycoside biosynthesis115
esculetin modification219
bixin biosynthesis313
superpathway of scopolin and esculin biosynthesis127
ponciretin biosynthesis05
ubiquinol-10 biosynthesis (eukaryotic)021
(+)-pisatin biosynthesis011
noscapine biosynthesis725
volatile cinnamoic ester biosynthesis016
spermidine biosynthesis I07
berberine biosynthesis032
capsaicin biosynthesis616
6-methoxymellein biosynthesis022
secologanin and strictosidine biosynthesis332
indole glucosinolate activation (intact plant cell)517
emetine biosynthesis515
colchicine biosynthesis018
ethylene biosynthesis I (plants)415
plastoquinol-9 biosynthesis I013
superpathway of polymethylated quercetin/quercetagetin glucoside biosynthesis (Chrysosplenium)234
superpathway of isoflavonoids (via naringenin)028
arctigenin and isoarctigenin biosynthesis36
rot-2'-enonate biosynthesis010
quercetin sulfate biosynthesis215
epoxypseudoisoeugenol-2-methylbutanoate biosynthesis016
ubiquinol-9 biosynthesis (eukaryotic)119
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis211
formononetin biosynthesis011
acridone alkaloid biosynthesis417
seleno-amino acid detoxification and volatilization III26
linear furanocoumarin biosynthesis120
1-methylpyrrolinium biosynthesis012
superpathway of hyoscyamine (atropine) and scopolamine biosynthesis039
ubiquinol-10 biosynthesis (late decarboxylation)021
Amino acids regulate mTORC1226
Diseases of programmed cell death3611
Cholesterol Biosynthesis and Metabolism2248
Juvenile Hormone Synthesis522
Arsenate Detoxification716
superpathway of ergosterol biosynthesis II133
magnoflorine biosynthesis08
tricin biosynthesis512
glucosinolate biosynthesis from tryptophan1229
epiberberine biosynthesis08
phytosterol biosynthesis (plants)1531
vanillin biosynthesis I111
methylsalicylate biosynthesis14
guaiacol biosynthesis25
superpathway of methylsalicylate metabolism311
vindoline, vindorosine and vinblastine biosynthesis240
Amaryllidacea alkaloids biosynthesis225
fluoroacetate and fluorothreonine biosynthesis016
3,8-divinyl-chlorophyllide a biosynthesis III (aerobic, light independent)023
Renz2020 - GEM of Human alveolar macrophage with SARS-CoV-20490
RAS processing1318
Defective pyroptosis47
Cellular response to starvation358
Sensory Perception21568
Drug ADME6387
Azathioprine ADME1626
Cobalamin (Cbl) metabolism722
avenanthramide biosynthesis021
ubiquinol-9 biosynthesis (late decarboxylation)019
Kleefstra syndrome04
10q22q23 copy number variation014
Maternal to zygotic transition (MZT)6017
Replacement of protamines by nucleosomes in the male pronucleus106
diphthamide biosynthesis111
spermine biosynthesis17
methionine salvage cycle III1028
(S)-reticuline biosynthesis116
superpathway of tryptophan utilization4292
spermidine biosynthesis17
mRNA capping48
ubiquinol-10 biosynthesis821
cysteine biosynthesis/homocysteine degradation (trans-sulfuration)113
cysteine biosynthesis519
superpathway of methionine degradation1945
methionine degradation410
secologanin and strictosidine biosynthesis1336
polymethylated quercetin glucoside biosynthesis I - quercetin series (Chrysosplenium)231
pinobanksin biosynthesis215
methylquercetin biosynthesis210
1,4-dihydroxy-6-naphthoate biosynthesis II714
1,4-dihydroxy-6-naphthoate biosynthesis I817
tricetin methylation26
8-methylmenaquinone biosynthesis25
vindoline and vinblastine biosynthesis635
polymethylated quercetin glucoside biosynthesis II - quercetagetin series (Chrysosplenium)238
superpathway of nicotine biosynthesis232
tricin biosynthesis612
homogalacturonan biosynthesis014
superpathway of seleno-compound metabolism744
fluoroacetate and fluorothreonine biosynthesis422
L-homocysteine biosynthesis725
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)1924
heme b biosynthesis III (from siroheme)113
heme b biosynthesis II (anaerobic)413
superpathway of heme b biosynthesis from uroporphyrinogen-III517
papaverine biosynthesis313
chelerythrine biosynthesis823
sanguinarine and macarpine biosynthesis839
palmatine biosynthesis09
berberine biosynthesis132
spermidine biosynthesis III511
glycine betaine biosynthesis IV (from glycine)412
spermidine biosynthesis I635
(aminomethyl)phosphonate degradation1231
10,13-epoxy-11-methyl-octadecadienoate biosynthesis25
caffeine biosynthesis I012
caffeine biosynthesis II (via paraxanthine)012
methyl indole-3-acetate interconversion013
seleno-amino acid detoxification and volatilization I05
scopoletin biosynthesis515
seleno-amino acid detoxification and volatilization II015
suberin monomers biosynthesis1342
coumarins biosynthesis (engineered)831
esculetin modification221
daphnetin modification115
linear furanocoumarin biosynthesis221
phenolphthiocerol biosynthesis1231
superpathway of demethylmenaquinol-6 biosynthesis II619
superpathway of scopolin and esculin biosynthesis131
superpathway of choline biosynthesis532
autoinducer CAI-1 biosynthesis214
autoinducer AI-2 biosynthesis I319
autoinducer AI-2 biosynthesis II (Vibrio)213
dimycocerosyl triglycosyl phenolphthiocerol biosynthesis1017
hydrogen sulfide biosynthesis II (mammalian)214
spinosyn A biosynthesis926
phthiocerol biosynthesis1320
isoflavonoid biosynthesis I120
(+)-pisatin biosynthesis015
diphthamide biosynthesis II (eukaryotes)613
free phenylpropanoid acid biosynthesis210
p-HBAD biosynthesis818
isoflavonoid biosynthesis II128
diphthamide biosynthesis I (archaea)212
ferulate and sinapate biosynthesis112
staphylopine biosynthesis39
stipitatate biosynthesis424
volatile cinnamoic ester biosynthesis216
superpathway of benzoxazinoid glucosides biosynthesis1020
sakuranetin biosynthesis112
t-anethole biosynthesis215
hesperitin glycoside biosynthesis011
gliotoxin inactivation17
dTDP-D-forosamine biosynthesis624
N-methylanthraniloyl-u03B2-D-glucopyranose biosynthesis38
molybdenum cofactor biosynthesis1823
L-nicotianamine biosynthesis24
superpathway of L-lysine degradation33112
polymethylated kaempferol biosynthesis110
histamine degradation424
dopamine degradation431
1,3,5-trimethoxybenzene biosynthesis67
3,8-divinyl-chlorophyllide a biosynthesis II (anaerobic)934
3,8-divinyl-chlorophyllide a biosynthesis III (aerobic, light independent)823
furaneol and mesifurane biosynthesis318
psilocybin biosynthesis016
diacylglyceryl-N,N,N-trimethylhomoserine biosynthesis24
aflatoxins B1 and G1 biosynthesis218
sulfur volatiles biosynthesis25
gossypol biosynthesis023
shinorine biosynthesis321
dimethyl sulfide biosynthesis from methionine210
toxoflavin biosynthesis318
anditomin biosynthesis1235
gliotoxin biosynthesis729
dTDP-L-mycarose biosynthesis1118
aflatoxins B2 and G2 biosynthesis313
sterigmatocystin biosynthesis210
gadusol biosynthesis211
heme degradation V213
juvenile hormone III biosynthesis I422
serotonin and melatonin biosynthesis717
geodin biosynthesis020
catecholamine biosynthesis328
aucuparin biosynthesis613
juvenile hormone III biosynthesis II116
dTDP-L-megosamine biosynthesis519
dTDP-D-ravidosamine and dTDP-4-acetyl-D-ravidosamine biosynthesis519
dTDP-D-olivose, dTDP-D-oliose and dTDP-D-mycarose biosynthesis618
dTDP-u03B2-L-evernitrose biosynthesis113
glutathione-mediated detoxification II1517
phosphatidylcholine biosynthesis II012
phosphatidylcholine biosynthesis III09
dTDP-4-O-demethyl-u03B2-L-noviose biosynthesis515
phosphatidylcholine biosynthesis V510
phosphatidylcholine biosynthesis IV010
dTDP-u03B2-L-4-epi-vancosamine biosynthesis520
dTDP-D-desosamine biosynthesis1422
noradrenaline and adrenaline degradation823
L-lysine fermentation to acetate and butanoate857
dTDP-u03B1-D-mycaminose biosynthesis415
noscapine biosynthesis1123
superpathway of ergotamine biosynthesis728
meleagrin biosynthesis011
Amaryllidacea alkaloids biosynthesis236
neoxaline biosynthesis08
acridone alkaloid biosynthesis317
fumitremorgin C biosynthesis518
viridicatin biosynthesis020
emetine biosynthesis520
superpathway of roquefortine, meleagrin and neoxaline biosynthesis022
u03B3-coniciene and coniine biosynthesis022
peramine biosynthesis110
N-methyl-u03941-pyrrolinium cation biosynthesis027
4'-methoxyviridicatin biosynthesis018
vitamin E biosynthesis (tocopherols)518
phylloquinol biosynthesis415
glycine betaine biosynthesis V (from glycine)07
Spermine Syn413
superpathway of polyamine biosynthesis I759
creatine biosynthesis411
spermidine hydroxycinnamic acid conjugates biosynthesis315
yersiniabactin biosynthesis415
superpathway of arginine and polyamine biosynthesis18101
factor 430 biosynthesis620
paromamine biosynthesis II522
superpathway of polyamine biosynthesis II920
phenylpropanoid biosynthesis1229
factor 420 biosynthesis522
brassicicene C biosynthesis518
tetrahydromethanopterin biosynthesis938
S-adenosyl-L-methionine biosynthesis519
FeMo cofactor biosynthesis614
polymethylated quercetin biosynthesis211
acacetin biosynthesis07
2'-deoxymugineic acid phytosiderophore biosynthesis1214
actinomycin D biosynthesis519
nevadensin biosynthesis013
blasticidin S biosynthesis925
3-methylarginine biosynthesis211
heme d1 biosynthesis412
roseoflavin biosynthesis119
prodigiosin biosynthesis1029
glucosinolate biosynthesis from tryptophan532
rebeccamycin biosynthesis723
cephamycin C biosynthesis216
6-methylpretetramide biosynthesis917
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis614
pyochelin biosynthesis314
elloramycin biosynthesis1525
superpathway of thiamine diphosphate biosynthesis III (eukaryotes)1225
superpathway of rifamycin B biosynthesis1354
nocardicin A biosynthesis619
superpathway of L-methionine biosynthesis (transsulfuration)959
L-methionine biosynthesis III928
thiocoraline biosynthesis415
dechlorogriseofulvin biosynthesis311
novobiocin biosynthesis1741
superpathway of L-homoserine and L-methionine biosynthesis649
superpathway of L-methionine biosynthesis (by sulfhydrylation)1955
gentamicin biosynthesis426
pyocyanin biosynthesis212
L-methionine biosynthesis I430
fosfomycin biosynthesis426
bacimethrin and bacimethrin pyrophosphate biosynthesis414
superpathway of penicillin, cephalosporin and cephamycin biosynthesis1169
tetracycline and oxytetracycline biosynthesis620
tetracenomycin C biosynthesis1020
superpathway of tetracycline and oxytetracycline biosynthesis1530
L-pyrrolysine biosynthesis313
phosalacine biosynthesis2049
daunorubicin biosynthesis1930
mithramycin biosynthesis1628
arginomycin biosynthesis722
L-methionine salvage cycle I (bacteria and plants)1938
staurosporine biosynthesis824
L-methionine salvage cycle III1029
L-methionine salvage cycle II (plants)832
phosphinothricin tripeptide biosynthesis1956
saframycin A biosynthesis618
lincomycin biosynthesis316
rifamycin B biosynthesis930
indolmycin biosynthesis830
aclacinomycin biosynthesis1428
puromycin biosynthesis227
echinomycin and triostin A biosynthesis618
dehydrophos biosynthesis1025
superpathway of L-cysteine biosynthesis (fungi)628
L-cysteine biosynthesis VI (from L-methionine)518
L-cysteine biosynthesis III (from L-homocysteine)322
superpathway of L-cysteine biosynthesis (mammalian)928
glyphosate degradation III718
superpathway of ergosterol biosynthesis II135
superpathway of ergosterol biosynthesis I2156
Escherichia coli serotype O9a O-antigen biosynthesis418
ergosterol biosynthesis I514
ergosterol biosynthesis II116
superpathway of sulfur amino acid biosynthesis (Saccharomyces cerevisiae)1043
superpathway of L-lysine, L-threonine and L-methionine biosynthesis I1994
7-dehydroporiferasterol biosynthesis118
rot-2'-enonate biosynthesis012
choline biosynthesis I021
choline biosynthesis II09
cob(II)yrinate a,c-diamide biosynthesis II (late cobalt incorporation)1444
cob(II)yrinate a,c-diamide biosynthesis I (early cobalt insertion)1731
salinosporamide A biosynthesis1129
okenone biosynthesis511
spirilloxanthin and 2,2'-diketo-spirilloxanthin biosynthesis515
tRNA methylation (yeast)103
5-(carboxymethoxy)uridine biosynthesis27
spheroidene and spheroidenone biosynthesis612
mRNA capping I58
wybutosine biosynthesis510
queuosine biosynthesis521
mRNA capping II38
methylwyosine biosynthesis59
tRNA-uridine 2-thiolation (bacteria)1019
tRNA-uridine 2-thiolation (cytoplasmic)910
u03B2-alanine betaine biosynthesis18
7-(3-amino-3-carboxypropyl)-wyosine biosynthesis610
L-dopa degradation117
2-methylisoborneol biosynthesis49
superpathway of bacteriochlorophyll a biosynthesis2270
bacteriochlorophyll e biosynthesis642
bacteriochlorophyll c biosynthesis1030
bacteriochlorophyll d biosynthesis524
siroheme biosynthesis811
superpathway of dTDP-glucose-derived antibiotic building blocks biosynthesis3139
superpathway of erythromycin biosynthesis1842
superpathway of pterocarpan biosynthesis (via formononetin)334
superpathway of megalomicin A biosynthesis842
oleandomycin biosynthesis720
superpathway of isoflavonoids (via naringenin)034
mycinamicin biosynthesis1224
erythromycin A biosynthesis212
superpathway of menaquinol-8 biosynthesis II524
superpathway of erythromycin biosynthesis (without sugar biosynthesis)823
menaquinol-8 biosynthesis15
superpathway of menaquinol-11 biosynthesis024
tylosin biosynthesis1426
menaquinol-12 biosynthesis09
superpathway of menaquinol-6 biosynthesis I324
menaquinol-9 biosynthesis05
yatein biosynthesis II112
superpathway of ubiquinol-6 biosynthesis (eukaryotic)527
superpathway of menaquinol-8 biosynthesis III722
superpathway of menaquinol-8 biosynthesis I1036
yatein biosynthesis I110
superpathway of menaquinol-12 biosynthesis024
menaquinol-13 biosynthesis09
plastoquinol-9 biosynthesis II317
menaquinol-10 biosynthesis09
superpathway of menaquinol-9 biosynthesis124
plastoquinol-9 biosynthesis I014
menaquinol-4 biosynthesis I03
menaquinol-7 biosynthesis29
superpathway of plastoquinol biosynthesis119
superpathway of hyoscyamine and scopolamine biosynthesis441
superpathway of menaquinol-13 biosynthesis024
superpathway of menaquinol-10 biosynthesis024
menaquinol-11 biosynthesis09
menaquinol-6 biosynthesis15
superpathway of menaquinol-7 biosynthesis925
methylphosphonate degradation I717
methylphosphonate degradation II116
superpathway of chorismate metabolism56186
ubiquinol-6 biosynthesis from 4-hydroxybenzoate (eukaryotic)519
ubiquinol-6 biosynthesis from 4-aminobenzoate (yeast)522
ubiquinol-10 biosynthesis (eukaryotic)821
ubiquinol-10 biosynthesis (prokaryotic)619
superpathway of flavones and derivatives biosynthesis1064
ubiquinol-6 bypass biosynthesis (eukaryotic)526
ubiquinol-7 biosynthesis (eukaryotic)019
ubiquinol-8 biosynthesis (eukaryotic)021
ubiquinol-7 biosynthesis (prokaryotic)019
ubiquinol-8 biosynthesis (prokaryotic)830
ubiquinol-9 biosynthesis (eukaryotic)221
ubiquinol-9 biosynthesis (prokaryotic)320
lipoate biosynthesis and incorporation II211
aspartate superpathway25122
superpathway of phylloquinol biosynthesis1636
superpathway of betalain biosynthesis252
superpathway of S-adenosyl-L-methionine biosynthesis961
betaxanthin biosynthesis010
hopanoid biosynthesis (bacteria)830
plant sterol biosynthesis1652
superpathway of ubiquinol-8 biosynthesis (prokaryotic)1141
botryococcenes and methylated squalene biosynthesis715
superpathway of avenacin A biosynthesis522
dimethylsulfoniopropanoate biosynthesis II (Spartina)022
dimethylsulfoniopropanoate biosynthesis I (Wollastonia)113
superpathway of phosphatidylcholine biosynthesis019
superpathway of fumitremorgin biosynthesis925
gibberellin inactivation II (methylation)216
chrysoeriol biosynthesis36
(S)-reticuline biosynthesis I128
(S)-reticuline biosynthesis II117
coniferyl alcohol 9-methyl ester biosynthesis29
6-gingerol biosynthesis05
epoxypseudoisoeugenol-2-methylbutanoate biosynthesis222
sterculate biosynthesis06
cyclopropane fatty acid (CFA) biosynthesis111
indole glucosinolate activation (intact plant cell)423
ergothioneine biosynthesis I (bacteria)522
ergothioneine biosynthesis II (fungi)215
5,6-dimethylbenzimidazole biosynthesis II (anaerobic)614
superpathway of L-methionine salvage and degradation2869
L-methionine degradation I (to L-homocysteine)818
ethylene biosynthesis I (plants)815
3-hydroxy-4-methyl-anthranilate biosynthesis I617
3-hydroxy-4-methyl-anthranilate biosynthesis II316
colchicine biosynthesis021
S-adenosyl-L-methionine cycle I417
kaempferide triglycoside biosynthesis118
eupatolitin 3-O-glucoside biosynthesis031
chanoclavine I aldehyde biosynthesis716
superpathway of polymethylated quercetin/quercetagetin glucoside biosynthesis (Chrysosplenium)246
ajmaline and sarpagine biosynthesis238
quercetin sulfate biosynthesis118
gramine biosynthesis19
polymethylated myricetin biosynthesis (tomato)220
ubiquinol-6 bypass biosynthesis426
methionine degradation I (to homocysteine)317
L-methionine biosynthesis323
superpathway of ergosterol biosynthesis2256
cysteine biosynthesis IV (fungi)628
tRNA methylation113
spermine and methylthioadenosine biosynthesis211
spermidine and methylthioadenosine biosynthesis210
ergosterol biosynthesis514
L-methionine biosynthesis II916
superpathway of polyamine biosynthesis312
superpathway of proto- and siroheme biosynthesis1640
26,27-dehydrozymosterol metabolism28
simple coumarins biosynthesis2823
biotin biosynthesis III015
streptorubin B biosynthesis020
adenosylcobalamin biosynthesis II (aerobic)060
transulfuration021
chlorophyllide a biosynthesis I (aerobic, light-dependent)1124
chlorophyllide a biosynthesis III (aerobic, light independent)1324
adenosylcobalamin biosynthesis II (late cobalt incorporation)2655
heme biosynthesis III (from siroheme)110
aminomethylphosphonate degradation419
diphthamide biosynthesis (archaea)111
Purine metabolism and related disorders2353
Cysteine and methionine catabolism1436
Yang cycle217
SAM cycle111
SMM cycle15
Beta-alanine betaine biosynthesis16
Methionine biosynthesis II017
Spermine biosynthesis06
Spermidine biosynthesis06
Biotin biosynthesis II113
Jasmonate biosynthesis216
Ethylene biosynthesis and signaling1116
Ethene biosynthesis from methionine114
Linear furanocoumarin biosynthesis015
Lignin biosynthesis221
Pinobanksin biosynthesis19
Pterocarpan biosynthesis07
Sterol biosynthesis525
Suberin biosynthesis022
Tricin biosynthesis315
Choline biosynthesis I014
Response to iron deficiency1017
Mugineic acid biosynthesis214
Nicotinate and Nicotinamide metabolism ( Nicotinate and Nicotinamide metabolism )2225
Arginine and Proline metabolism ( Arginine and Proline metabolism )4255
Glycine and Serine metabolism ( Glycine and Serine metabolism )3649
Histidine degradation ( Histidine degradation )2326
Methionine and Cysteine metabolism ( Methionine and Cysteine metabolism )2342
Tryptophan degradation ( Tryptophan degradation )6454
Tyrosine metabolism ( Tyrosine metabolism )2841
Nsp9 interactions (COVID-19 Disease Map)8330
superpathway of sterol biosynthesis050
ubiquinone-9 biosynthesis09
ovothiol A biosynthesis05
methionine biosynthesis020
superpathway of phospholipid biosynthesis027
ester phospholipid biosynthesis021
superpathway of lysine, threonine and methionine biosynthesis II032
methionine and S-adenosylmethionine synthesis010
S-adenosylmethionine biosynthesis07
heme biosynthesis from uroporphyrinogen-III II012
methionine biosynthesis II018
Kennedy pathway012
Trans-sulfuration and one-carbon metabolism020
Trans-sulfuration pathway014
Trans-sulfuration, one-carbon metabolism and related pathways053
Kennedy pathway from sphingolipids011
One-carbon metabolism and related pathways038
MTHFR deficiency1515
Disorders of folate metabolism and transport1827
Methionine metabolism leading to sulfur amino acids and related disorders919

Protein Targets (9)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Protein arginine N-methyltransferase 1Homo sapiens (human)IC50 (µMol)12.00000.25003.61679.4000AID476872
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Met repressor Escherichia coliEC50 (µMol)0.01730.01730.01730.0173AID642180
Met repressor Escherichia coliKd0.00400.00400.00400.0040AID642179
Protein arginine N-methyltransferase 5Homo sapiens (human)Kd0.55000.55000.60550.6610AID1825281
Phenylethanolamine N-methyltransferaseHomo sapiens (human)Kd8.10004.80006.72507.5000AID282842; AID282843; AID282844; AID282845; AID282846; AID282847
Methylosome protein 50Homo sapiens (human)Kd0.55000.55000.60550.6610AID1825281
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Phenylethanolamine N-methyltransferaseHomo sapiens (human)Km6.51671.20005.48009.6000AID282842; AID282843; AID282844; AID282845; AID282846; AID282847
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (53)

Processvia Protein(s)Taxonomy
peptidyl-arginine N-methylationProtein arginine N-methyltransferase 5Homo sapiens (human)
spliceosomal snRNP assemblyProtein arginine N-methyltransferase 5Homo sapiens (human)
chromatin remodelingProtein arginine N-methyltransferase 5Homo sapiens (human)
DNA-templated transcription terminationProtein arginine N-methyltransferase 5Homo sapiens (human)
regulation of mitotic nuclear divisionProtein arginine N-methyltransferase 5Homo sapiens (human)
peptidyl-arginine methylationProtein arginine N-methyltransferase 5Homo sapiens (human)
circadian regulation of gene expressionProtein arginine N-methyltransferase 5Homo sapiens (human)
endothelial cell activationProtein arginine N-methyltransferase 5Homo sapiens (human)
negative regulation of gene expression via chromosomal CpG island methylationProtein arginine N-methyltransferase 5Homo sapiens (human)
negative regulation of cell differentiationProtein arginine N-methyltransferase 5Homo sapiens (human)
negative regulation of DNA-templated transcriptionProtein arginine N-methyltransferase 5Homo sapiens (human)
positive regulation of mRNA splicing, via spliceosomeProtein arginine N-methyltransferase 5Homo sapiens (human)
positive regulation of oligodendrocyte differentiationProtein arginine N-methyltransferase 5Homo sapiens (human)
regulation of ERK1 and ERK2 cascadeProtein arginine N-methyltransferase 5Homo sapiens (human)
Golgi ribbon formationProtein arginine N-methyltransferase 5Homo sapiens (human)
liver regenerationProtein arginine N-methyltransferase 5Homo sapiens (human)
regulation of signal transduction by p53 class mediatorProtein arginine N-methyltransferase 5Homo sapiens (human)
positive regulation of adenylate cyclase-inhibiting dopamine receptor signaling pathwayProtein arginine N-methyltransferase 5Homo sapiens (human)
regulation of DNA-templated transcriptionProtein arginine N-methyltransferase 5Homo sapiens (human)
methylationPhenylethanolamine N-methyltransferaseHomo sapiens (human)
epinephrine biosynthetic processPhenylethanolamine N-methyltransferaseHomo sapiens (human)
catecholamine biosynthetic processPhenylethanolamine N-methyltransferaseHomo sapiens (human)
protein methylationProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
protein repairProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
in utero embryonic developmentProtein arginine N-methyltransferase 1Homo sapiens (human)
protein methylationProtein arginine N-methyltransferase 1Homo sapiens (human)
DNA damage responseProtein arginine N-methyltransferase 1Homo sapiens (human)
cell surface receptor signaling pathwayProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of cell population proliferationProtein arginine N-methyltransferase 1Homo sapiens (human)
RNA splicingProtein arginine N-methyltransferase 1Homo sapiens (human)
peptidyl-arginine methylationProtein arginine N-methyltransferase 1Homo sapiens (human)
viral protein processingProtein arginine N-methyltransferase 1Homo sapiens (human)
regulation of BMP signaling pathwayProtein arginine N-methyltransferase 1Homo sapiens (human)
neuron projection developmentProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of erythrocyte differentiationProtein arginine N-methyltransferase 1Homo sapiens (human)
regulation of megakaryocyte differentiationProtein arginine N-methyltransferase 1Homo sapiens (human)
negative regulation of megakaryocyte differentiationProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of translationProtein arginine N-methyltransferase 1Homo sapiens (human)
negative regulation of JNK cascadeProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of hemoglobin biosynthetic processProtein arginine N-methyltransferase 1Homo sapiens (human)
cardiac muscle tissue developmentProtein arginine N-methyltransferase 1Homo sapiens (human)
protein homooligomerizationProtein arginine N-methyltransferase 1Homo sapiens (human)
cellular response to methionineProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of p38MAPK cascadeProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of TORC1 signalingProtein arginine N-methyltransferase 1Homo sapiens (human)
positive regulation of double-strand break repair via homologous recombinationProtein arginine N-methyltransferase 1Homo sapiens (human)
chromatin remodelingProtein arginine N-methyltransferase 1Homo sapiens (human)
peptidyl-arginine methylation, to asymmetrical-dimethyl arginineProtein arginine N-methyltransferase 1Homo sapiens (human)
protein polyubiquitinationMethylosome protein 50Homo sapiens (human)
spliceosomal snRNP assemblyMethylosome protein 50Homo sapiens (human)
regulation of transcription by RNA polymerase IIMethylosome protein 50Homo sapiens (human)
ubiquitin-dependent protein catabolic processMethylosome protein 50Homo sapiens (human)
positive regulation of cell population proliferationMethylosome protein 50Homo sapiens (human)
positive regulation of DNA-templated transcriptionMethylosome protein 50Homo sapiens (human)
positive regulation of mRNA splicing, via spliceosomeMethylosome protein 50Homo sapiens (human)
secretory columnal luminar epithelial cell differentiation involved in prostate glandular acinus developmentMethylosome protein 50Homo sapiens (human)
epithelial cell proliferation involved in prostate gland developmentMethylosome protein 50Homo sapiens (human)
negative regulation of epithelial cell proliferation involved in prostate gland developmentMethylosome protein 50Homo sapiens (human)
oocyte axis specificationMethylosome protein 50Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (29)

Processvia Protein(s)Taxonomy
p53 bindingProtein arginine N-methyltransferase 5Homo sapiens (human)
transcription corepressor activityProtein arginine N-methyltransferase 5Homo sapiens (human)
protein bindingProtein arginine N-methyltransferase 5Homo sapiens (human)
methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
methyl-CpG bindingProtein arginine N-methyltransferase 5Homo sapiens (human)
protein-arginine N-methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
protein-arginine omega-N symmetric methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
histone methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
identical protein bindingProtein arginine N-methyltransferase 5Homo sapiens (human)
ribonucleoprotein complex bindingProtein arginine N-methyltransferase 5Homo sapiens (human)
histone H4R3 methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
protein heterodimerization activityProtein arginine N-methyltransferase 5Homo sapiens (human)
E-box bindingProtein arginine N-methyltransferase 5Homo sapiens (human)
histone H3 methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
histone arginine N-methyltransferase activityProtein arginine N-methyltransferase 5Homo sapiens (human)
phenylethanolamine N-methyltransferase activityPhenylethanolamine N-methyltransferaseHomo sapiens (human)
protein bindingPhenylethanolamine N-methyltransferaseHomo sapiens (human)
protein-L-isoaspartate (D-aspartate) O-methyltransferase activityProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
protein bindingProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
cadherin bindingProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
RNA bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
protein bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
N-methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
protein methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
methyl-CpG bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
protein-arginine N-methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
enzyme bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
protein-arginine omega-N monomethyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
protein-arginine omega-N asymmetric methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
histone methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
identical protein bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
histone H4R3 methyltransferase activityProtein arginine N-methyltransferase 1Homo sapiens (human)
mitogen-activated protein kinase p38 bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
GATOR1 complex bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
S-adenosyl-L-methionine bindingProtein arginine N-methyltransferase 1Homo sapiens (human)
protein bindingMethylosome protein 50Homo sapiens (human)
methyl-CpG bindingMethylosome protein 50Homo sapiens (human)
nuclear receptor coactivator activityMethylosome protein 50Homo sapiens (human)
ubiquitin-like ligase-substrate adaptor activityMethylosome protein 50Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (12)

Processvia Protein(s)Taxonomy
nucleusProtein arginine N-methyltransferase 5Homo sapiens (human)
nucleoplasmProtein arginine N-methyltransferase 5Homo sapiens (human)
Golgi apparatusProtein arginine N-methyltransferase 5Homo sapiens (human)
cytosolProtein arginine N-methyltransferase 5Homo sapiens (human)
methylosomeProtein arginine N-methyltransferase 5Homo sapiens (human)
chromatinProtein arginine N-methyltransferase 5Homo sapiens (human)
cytoplasmProtein arginine N-methyltransferase 5Homo sapiens (human)
histone methyltransferase complexProtein arginine N-methyltransferase 5Homo sapiens (human)
cytosolProtein arginine N-methyltransferase 5Homo sapiens (human)
nucleusProtein arginine N-methyltransferase 5Homo sapiens (human)
cytosolPhenylethanolamine N-methyltransferaseHomo sapiens (human)
cytosolPhenylethanolamine N-methyltransferaseHomo sapiens (human)
cytosolProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
extracellular exosomeProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
extracellular vesicleProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
cytoplasmProtein-L-isoaspartate(D-aspartate) O-methyltransferaseHomo sapiens (human)
lysosomal membraneProtein arginine N-methyltransferase 1Homo sapiens (human)
nucleusProtein arginine N-methyltransferase 1Homo sapiens (human)
nucleoplasmProtein arginine N-methyltransferase 1Homo sapiens (human)
cytoplasmProtein arginine N-methyltransferase 1Homo sapiens (human)
cytosolProtein arginine N-methyltransferase 1Homo sapiens (human)
methylosomeProtein arginine N-methyltransferase 1Homo sapiens (human)
nucleusProtein arginine N-methyltransferase 1Homo sapiens (human)
nucleusMethylosome protein 50Homo sapiens (human)
nucleoplasmMethylosome protein 50Homo sapiens (human)
cytoplasmMethylosome protein 50Homo sapiens (human)
Golgi apparatusMethylosome protein 50Homo sapiens (human)
cytosolMethylosome protein 50Homo sapiens (human)
methylosomeMethylosome protein 50Homo sapiens (human)
Cul4B-RING E3 ubiquitin ligase complexMethylosome protein 50Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (63)

Assay IDTitleYearJournalArticle
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1347160Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347159Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1133261Retardation factor, Rf of the compound on silica gel GF containing 5% Na2HPO4 by chromatography1978Journal of medicinal chemistry, Dec, Volume: 21, Issue:12
Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 7. Role of the ribosyl moiety in enzymatic binding of S-adenosyl-L-homocysteine and S-adenosyl-L-methionine.
AID1079934Highest frequency of acute liver toxicity observed during clinical trials, expressed as a percentage. [column '% AIGUE' in source]
AID282847Activity of human PNMT D267N mutant assessed as phenylethanolamine methylation2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase.
AID282842Activity of human wild type PNMT assessed as phenylethanolamine methylation2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase.
AID613026Binding affinity to 2-amino purine labelled SAM2 riboswitch aptamer assessed as change in fluorescence at 5 mM to 10 mM at pH 8.3 by fluorescence binding assay2011Bioorganic & medicinal chemistry letters, Sep-01, Volume: 21, Issue:17
Rational design of SAM analogues targeting SAM-II riboswitch aptamer.
AID199771Time required for the half inactivation of S-Adenosyl-L-methionine decarboxylase was determined with 0.2 mM of compound along with 1 mM NaBH3CN1982Journal of medicinal chemistry, May, Volume: 25, Issue:5
Synthesis and biochemical properties of chemically stable product analogues of the reaction catalyzed by S-adenosyl-L-methionine decarboxylase.
AID199921Tested for kinetic constant (Vmax) of compound for S-adenosyl-L-methionine decarboxylase1980Journal of medicinal chemistry, Feb, Volume: 23, Issue:2
Inhibitors of polyamine biosynthesis. 8. Irreversible inhibition of mammalian S-adenosyl-L-methionine decarboxylase by substrate analogues.
AID1079945Animal toxicity known. [column 'TOXIC' in source]
AID498926Activity at Salinispora tropica CNB-440 wild type recombinant SalL expressed in Escherichia coli BL21(DE3) after 30 mins by HPLC analysis2008Nature chemical biology, Jan, Volume: 4, Issue:1
Discovery and characterization of a marine bacterial SAM-dependent chlorinase.
AID199770Time required for the half inactivation of S-Adenosyl-L-methionine decarboxylase was determined with 0.2 mM of compound1982Journal of medicinal chemistry, May, Volume: 25, Issue:5
Synthesis and biochemical properties of chemically stable product analogues of the reaction catalyzed by S-adenosyl-L-methionine decarboxylase.
AID1079931Moderate liver toxicity, defined via clinical-chemistry results: ALT or AST serum activity 6 times the normal upper limit (N) or alkaline phosphatase serum activity of 1.7 N. Value is number of references indexed. [column 'BIOL' in source]
AID199920Km of compound for S-adenosyl-L-methionine decarboxylase1980Journal of medicinal chemistry, Feb, Volume: 23, Issue:2
Inhibitors of polyamine biosynthesis. 8. Irreversible inhibition of mammalian S-adenosyl-L-methionine decarboxylase by substrate analogues.
AID27327Apparent kinetic activity measured for protein carboxyl methyltransferase in Leishmania donovani promastigotes1991Journal of medicinal chemistry, Sep, Volume: 34, Issue:9
Synthesis and biological activity of sinefungin analogues.
AID1079944Benign tumor, proven histopathologically. Value is number of references indexed. [column 'T.BEN' in source]
AID1079940Granulomatous liver disease, proven histopathologically. Value is number of references indexed. [column 'GRAN' in source]
AID199909Tested for S-adenosyl-L-methionine decarboxylase activity recovered after 40 min of 0.2 nM +1 mM NaBH3CN compound in incubation media1980Journal of medicinal chemistry, Feb, Volume: 23, Issue:2
Inhibitors of polyamine biosynthesis. 8. Irreversible inhibition of mammalian S-adenosyl-L-methionine decarboxylase by substrate analogues.
AID282846Activity of human PNMT D267A mutant assessed as phenylethanolamine methylation2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase.
AID327641Activity of Thermotoga maritima S-adenosyl-homocysteine deaminase Tm0936 assessed as ammonia production2007Nature, Aug-16, Volume: 448, Issue:7155
Structure-based activity prediction for an enzyme of unknown function.
AID282845Activity of human PNMT E219A mutant assessed as phenylethanolamine methylation2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase.
AID199779Time required for the half inactivation of S-Adenosyl-L-methionine decarboxylase was determined with 1 mM of compound1982Journal of medicinal chemistry, May, Volume: 25, Issue:5
Synthesis and biochemical properties of chemically stable product analogues of the reaction catalyzed by S-adenosyl-L-methionine decarboxylase.
AID164154Kinetic constant was measured for PMII of Leishmania donovani promastigotes using supernatant (S12) fraction1992Journal of medicinal chemistry, Jan, Volume: 35, Issue:1
Total synthesis of uracil analogues of sinefungin.
AID1079948Times to onset, minimal and maximal, observed in the indexed observations. [column 'DELAI' in source]
AID1079936Choleostatic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is < 2 (see ACUTE). Value is number of references indexed. [column 'CHOLE' in source]
AID1079946Presence of at least one case with successful reintroduction. [column 'REINT' in source]
AID476872Inhibition of GST-fused human recombinant PRMT1 after 90 mins by SDS-PAGE based scintillation counting2010Bioorganic & medicinal chemistry letters, Apr-01, Volume: 20, Issue:7
Toward the development of potent and selective bisubstrate inhibitors of protein arginine methyltransferases.
AID638162Activity of Paramecium bursaria Chlorella virus 1 vSET domain protein Y109G mutant methyltransferase activity expressed in Escherichia coli BL21 (DE3) cells assessed as trimethylation at histone H3 lysine 27 residue measured after 30 mins by Michaelis-Men2011Journal of medicinal chemistry, Nov-10, Volume: 54, Issue:21
Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.
AID642179Binding affinity to Escherichia coli metJ in presence of operator DNA complex by filter binding study2012Bioorganic & medicinal chemistry letters, Jan-01, Volume: 22, Issue:1
Design, synthesis and in vitro evaluation of novel bivalent S-adenosylmethionine analogues.
AID638161Activity of wild type Paramecium bursaria Chlorella virus 1 vSET domain protein methyltransferase activity expressed in Escherichia coli BL21 (DE3) cells assessed as trimethylation at histone H3 lysine 27 residue measured after 30 mins by Michaelis-Menten2011Journal of medicinal chemistry, Nov-10, Volume: 54, Issue:21
Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.
AID638247Activity of Paramecium bursaria Chlorella virus 1 vSET domain protein L116A mutant methyltransferase activity expressed in Escherichia coli BL21 (DE3) cells assessed as trimethylation at histone H3 lysine 27 residue measured after 30 mins by Michaelis-Men2011Journal of medicinal chemistry, Nov-10, Volume: 54, Issue:21
Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.
AID1079932Highest frequency of moderate liver toxicity observed during clinical trials, expressed as a percentage. [column '% BIOL' in source]
AID1079943Malignant tumor, proven histopathologically. Value is number of references indexed. [column 'T.MAL' in source]
AID1079942Steatosis, proven histopathologically. Value is number of references indexed. [column 'STEAT' in source]
AID164153Kinetic constant was measured for PMII of Leishmania donovani promastigotes using protein extracted from the 12000 g pellet (P12).1992Journal of medicinal chemistry, Jan, Volume: 35, Issue:1
Total synthesis of uracil analogues of sinefungin.
AID50099In vitro inhibitory activity against Catechol-O-methyltransferase from porcine liver1997Journal of medicinal chemistry, Jun-20, Volume: 40, Issue:13
Synthesis and in vitro evaluation of two progressive series of bifunctional polyhydroxybenzamide catechol-O-methyltransferase inhibitors.
AID642180Binding affinity to Escherichia coli metJ assessed as protein dimer-DNA complex formation using F-metC operator DNA by fluorescence anisotropy2012Bioorganic & medicinal chemistry letters, Jan-01, Volume: 22, Issue:1
Design, synthesis and in vitro evaluation of novel bivalent S-adenosylmethionine analogues.
AID1133262Retardation factor, Rf of the compound on silica gel GF containing EtOH-HOAc-H2O (20:2:2)/0.1 M phosphate buffer at 7.4 by chromatography1978Journal of medicinal chemistry, Dec, Volume: 21, Issue:12
Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 7. Role of the ribosyl moiety in enzymatic binding of S-adenosyl-L-homocysteine and S-adenosyl-L-methionine.
AID1079939Cirrhosis, proven histopathologically. Value is number of references indexed. [column 'CIRRH' in source]
AID327642Ratio of Kcat to Km for Thermotoga maritima S-adenosyl-homocysteine deaminase Tm0936 assessed as ammonia production2007Nature, Aug-16, Volume: 448, Issue:7155
Structure-based activity prediction for an enzyme of unknown function.
AID199908Tested for S-adenosyl-L-methionine decarboxylase activity recovered after 40 min of 0.2 nM compound in incubation media1980Journal of medicinal chemistry, Feb, Volume: 23, Issue:2
Inhibitors of polyamine biosynthesis. 8. Irreversible inhibition of mammalian S-adenosyl-L-methionine decarboxylase by substrate analogues.
AID282843Activity of human PNMT V53A mutant assessed as phenylethanolamine methylation2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase.
AID498929Ratio of Kcat to Km for Salinispora tropica CNB-440 wild type recombinant SalL expressed in Escherichia coli BL21(DE3)2008Nature chemical biology, Jan, Volume: 4, Issue:1
Discovery and characterization of a marine bacterial SAM-dependent chlorinase.
AID1079938Chronic liver disease either proven histopathologically, or through a chonic elevation of serum amino-transferase activity after 6 months. Value is number of references indexed. [column 'CHRON' in source]
AID1079941Liver damage due to vascular disease: peliosis hepatitis, hepatic veno-occlusive disease, Budd-Chiari syndrome. Value is number of references indexed. [column 'VASC' in source]
AID638248Ratio of Kcat to Km for wild type Paramecium bursaria Chlorella virus 1 vSET methyltransferase activity expressed in Escherichia coli BL21 (DE3) cells assessed as trimethylation at histone H3 lysine 27 residue measured after 30 mins by Michaelis-Menten eq2011Journal of medicinal chemistry, Nov-10, Volume: 54, Issue:21
Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.
AID199778In vitro inhibitory activity against S-adenosyl-L-methionine decarboxylase using liver from rat in presence of 1 mM putrescine1982Journal of medicinal chemistry, May, Volume: 25, Issue:5
Synthesis and biochemical properties of chemically stable product analogues of the reaction catalyzed by S-adenosyl-L-methionine decarboxylase.
AID282844Activity of human PNMT K57A mutant assessed as phenylethanolamine methylation2005Journal of medicinal chemistry, Nov-17, Volume: 48, Issue:23
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase.
AID199775In vitro inhibitory activity against S-adenosyl-L-methionine decarboxylase using liver from rat in absence of putrescine1982Journal of medicinal chemistry, May, Volume: 25, Issue:5
Synthesis and biochemical properties of chemically stable product analogues of the reaction catalyzed by S-adenosyl-L-methionine decarboxylase.
AID638250Ratio of Kcat to Km for Paramecium bursaria Chlorella virus 1 vSET domain protein L116A mutant methyltransferase activity expressed in Escherichia coli BL21 (DE3) cells assessed as trimethylation at histone H3 lysine 27 residue measured after 30 mins by M2011Journal of medicinal chemistry, Nov-10, Volume: 54, Issue:21
Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.
AID1079933Acute liver toxicity defined via clinical observations and clear clinical-chemistry results: serum ALT or AST activity > 6 N or serum alkaline phosphatases activity > 1.7 N. This category includes cytolytic, choleostatic and mixed liver toxicity. Value is
AID199903Time required for the half inactivation of S-adenosyl-L-methionine decarboxylase with 1 mM of compound along with 0.05 mM of [5-(6-Amino-purin-9-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl]-dimethyl-sulfonium; iodide1982Journal of medicinal chemistry, May, Volume: 25, Issue:5
Synthesis and biochemical properties of chemically stable product analogues of the reaction catalyzed by S-adenosyl-L-methionine decarboxylase.
AID199916Tested for S-adenosyl-L-methionine decarboxylase activity recovered after 80 min of 0.2 nM compound in incubation media1980Journal of medicinal chemistry, Feb, Volume: 23, Issue:2
Inhibitors of polyamine biosynthesis. 8. Irreversible inhibition of mammalian S-adenosyl-L-methionine decarboxylase by substrate analogues.
AID638249Ratio of Kcat to Km for Paramecium bursaria Chlorella virus 1 vSET domain protein Y109G mutant methyltransferase activity expressed in Escherichia coli BL21 (DE3) cells assessed as trimethylation at histone H3 lysine 27 residue measured after 30 mins by M2011Journal of medicinal chemistry, Nov-10, Volume: 54, Issue:21
Structure-guided design of a methyl donor cofactor that controls a viral histone H3 lysine 27 methyltransferase activity.
AID1079935Cytolytic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is > 5 (see ACUTE). Value is number of references indexed. [column 'CYTOL' in source]
AID1079947Comments (NB not yet translated). [column 'COMMENTAIRES' in source]
AID1079949Proposed mechanism(s) of liver damage. [column 'MEC' in source]
AID1079937Severe hepatitis, defined as possibly life-threatening liver failure or through clinical observations. Value is number of references indexed. [column 'MASS' in source]
AID1825281Inhibition of streptavidin sensor chip immobilized biotinylated human PRMT5/MEP50 assessed as dissociation constant by SPR analysis2022Journal of medicinal chemistry, 02-10, Volume: 65, Issue:3
Fragment-Based Discovery of MRTX1719, a Synthetic Lethal Inhibitor of the PRMT5•MTA Complex for the Treatment of
AID1799779Calorimetric (ITC) Assay from Article 10.1074/jbc.M111.290619: \\Thermodynamic evaluation of ligand binding in the plant-like phosphoethanolamine methyltransferases of the parasitic nematode Haemonchus contortus.\\2011The Journal of biological chemistry, Nov-04, Volume: 286, Issue:44
Thermodynamic evaluation of ligand binding in the plant-like phosphoethanolamine methyltransferases of the parasitic nematode Haemonchus contortus.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6,970)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901857 (26.64)18.7374
1990's829 (11.89)18.2507
2000's1421 (20.39)29.6817
2010's2094 (30.04)24.3611
2020's769 (11.03)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 61.09

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index61.09 (24.57)
Research Supply Index7.13 (2.92)
Research Growth Index5.77 (4.65)
Search Engine Demand Index165.16 (26.88)
Search Engine Supply Index3.20 (0.95)

This Compound (61.09)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials198 (3.31%)5.53%
Trials72 (6.11%)5.53%
Trials0 (0.00%)5.53%
Reviews590 (9.85%)6.00%
Reviews56 (4.75%)6.00%
Reviews0 (0.00%)6.00%
Case Studies49 (0.82%)4.05%
Case Studies110 (9.33%)4.05%
Case Studies0 (0.00%)4.05%
Observational3 (0.05%)0.25%
Observational16 (1.36%)0.25%
Observational0 (0.00%)0.25%
Other5,147 (85.97%)84.16%
Other925 (78.46%)84.16%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]