Page last updated: 2024-12-10

tocotrienol, delta

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Occurs in Manufacturing Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

delta-tocotrienol : A tocotrienol that is chroman-6-ol substituted by methyl groups at positions 2 and 8 and a farnesyl chain at position 2. [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]

Cross-References

ID SourceID
PubMed CID5282350
CHEMBL ID121305
CHEBI ID33276
SCHEMBL ID8408117
SCHEMBL ID16430161
MeSH IDM0218857

Synonyms (48)

Synonym
BIDD:PXR0041
delta-tocotrienols
CHEBI:33276 ,
(2r)-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2h-chromen-6-ol
6-chromanol, 2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)- (7ci,8ci)
8-methyltocotrienol
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-, (2r)-
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-, (2r)- (9ci)
(r)-delta-tocotrienol
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-, [r-(e,e)]-
tocotrienol, delta
25612-59-3
delta-tocotrienol
CHEMBL121305
2r,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2h-chromen-6-ol
LMPR02020056
(2r)-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-6-ol
unii-1srb74owsi
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-, (r-(e,e))-
1srb74owsi ,
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-((3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrienyl)-, (2r)-
j17.358d ,
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-((3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrien-1-yl)-, (2r)-
delta tocotrienol [who-dd]
.delta.-tocotrienol
d-delta-tocotrienol
(r)-.delta.-tocotrienol
6-chromanol, 2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-
(r)-2,8-dimethyl-2-((3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl)chroman-6-ol
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrien-1-yl]-, (2r)-
SCHEMBL8408117
HMS3650C18
DTXSID30180288
SCHEMBL16430161
delta-tocotrienol, analytical standard
NCGC00253541-03
2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-6-chromanol
3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-2h-1-benzopyran-6-ol, 9ci
Q27104272
SR-01000946270-1
sr-01000946270
(r-(e,e))-3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-2h-1-benzopyran-6-ol
delta -tocotrienol
r-delta-tocotrienol
HY-122778
CS-0089253
AS-82630
AKOS040760094

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Neither drug produced detectable toxic effects in any other tissue at the doses tested."( Acute toxicity of subcutaneously administered vitamin E isomers delta- and gamma-tocotrienol in mice.
Chakraborty, K; Ghosh, SP; Lombardini, E; Pessu, RL; Swift, SN; Villa, V,
)
0.13
" One patient had a drug-related adverse event (diarrhea) at a 3200-mg daily dose level."( A Phase I Safety, Pharmacokinetic, and Pharmacodynamic Presurgical Trial of Vitamin E δ-tocotrienol in Patients with Pancreatic Ductal Neoplasia.
Centeno, B; Chen, DT; Husain, K; Hutchinson, TZ; Lush, RM; Malafa, MP; Neuger, A; Sebti, S; Springett, GM, 2015
)
0.42
"No drug-related adverse events were observed."( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites.
Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016
)
0.43

Pharmacokinetics

ExcerptReferenceRelevance
" Pharmacokinetic data were derived from high-performance liquid chromatography (HPLC) assays."( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites.
Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016
)
0.43
" Pharmacokinetic parameters for single and multiple doses were, respectively, as follows (shown as range): time to maximum concentration of 4-9."( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites.
Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016
)
0.43

Bioavailability

ExcerptReferenceRelevance
"We have investigated the pharmacokinetics and bioavailability of alpha-, gamma- and delta-tocotrienols under fed and fasted conditions in eight healthy volunteers."( Pharmacokinetics and bioavailability of alpha-, gamma- and delta-tocotrienols under different food status.
Wong, JW; Yap, SP; Yuen, KH, 2001
)
0.31
"A study was conducted to evaluate the bioavailability of alpha-, gamma- and delta-tocotrienols administered via oral, intravenous, intramuscular and intraperitoneal routes in rats."( Influence of route of administration on the absorption and disposition of alpha-, gamma- and delta-tocotrienols in rats.
Lim, AB; Yap, SP; Yuen, KH, 2003
)
0.32
"A single dose comparative bioavailability study was conducted to evaluate the bioavailability of tocotrienols from two self-emulsifying formulations, one of which produced an emulsion that readily lipolysed under in vitro condition (SES-A), while the other produced a finer dispersion with negligible lipolysis (SES-B) in comparison with that of a non-self-emulsifying formulation in soya oil."( Influence of lipolysis and droplet size on tocotrienol absorption from self-emulsifying formulations.
Yap, SP; Yuen, KH, 2004
)
0.32
" This single-dose, randomized, crossover study aimed to compare the safety and bioavailability of a new formulation of Gamma Delta Tocotrienol (GDT) in comparison with the existing Tocotrienol-rich Fraction (TRF) in terms of gamma and delta isomers in healthy volunteers."( A new formulation of Gamma Delta Tocotrienol has superior bioavailability compared to existing Tocotrienol-Rich Fraction in healthy human subjects.
Bhoo-Pathy, N; Chik, Z; Choudhury, RB; Fuang, HG; Jabir, RS; Meganathan, P; Nesaretnam, K; Taib, NA, 2015
)
0.42
" Plasma tocotrienols were significantly increased after VEDT administration, indicating oral bioavailability of VEDT in humans."( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites.
Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016
)
0.43
" FA significantly increased the intracellular concentration of δ-T3, suggesting that FA improved the bioavailability of δ-T3, thereby increasing the inhibitory potency of δ-T3 on telomerase."( A Combination of δ-Tocotrienol and Ferulic Acid Synergistically Inhibits Telomerase Activity in DLD-1 Human Colorectal Adenocarcinoma Cells.
Eitsuka, T; Miyazawa, T; Nakagawa, K; Nishida, H; Tatewaki, N, 2016
)
0.43
"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

Dosage Studied

ExcerptRelevanceReference
" The tocotrienol-rich fraction (TRF) of palm oil inhibited growth of MCF7 cells in both the presence and absence of estradiol with a nonlinear dose-response but such that complete suppression of growth was achieved at 8 microg/mL."( Tocotrienols inhibit the growth of human breast cancer cells irrespective of estrogen receptor status.
Darbre, P; Dils, R; Nesaretnam, K; Stephen, R, 1998
)
0.3
" Tocotrienols were measured in heart, liver and adipose tissue showing that chronic oral dosage delivered tocotrienols to these organs despite low or no detection of tocotrienols in plasma."( Anti-inflammatory γ- and δ-tocotrienols improve cardiovascular, liver and metabolic function in diet-induced obese rats.
Brown, L; Fong, CW; Ward, LC; Wong, WY; Yap, WN, 2017
)
0.46
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Occurs in Manufacturing (3 Product(s))

Product Categories

Product CategoryProducts
Professional Supplements1
Vitamins & Supplements2

Products

ProductBrandCategoryCompounds Matched from IngredientsDate Retrieved
Dr. Mercola Vitamin E -- 30 CapsulesDr. MercolaProfessional Supplementsd-Beta Tocopherol, d-Alpha-Tocopherol, d-delta tocopherol, d-Gamma Tocopherol, d-Gamma Tocotrienol, Vitamin E, d-Alpha Tocotrienol, d-Beta Tocotrienol, d-Delta Tocotrienol2024-11-29 10:47:42
NutriCology Tocomin SupraBio Tocotrienols -- 200 mg - 60 SoftgelsNutriCologyVitamins & SupplementsVitamin E, d-Gamma Tocotrienol, Vitamin E, glycerin, d-Alpha Tocotrienol, d-Beta Tocotrienol, d-delta tocotrienol2024-11-29 10:47:42
Olympian Labs Tocomin Vitamin E Complete -- 60 SoftgelsOlympian LabsVitamins & Supplementsd-Beta Tocopherol, Vitamin E, d-delta tocopherol, d-Gamma Tocopherol, d-Gamma Tocotrienol, Vitamin E, Phytosterols, d-Alpha Tocotrienol, d-Beta Tocotrienol, d-delta tocotrienol2024-11-29 10:47:42

Roles (8)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
NF-kappaB inhibitorAn inhibitor of NF-kappaB (nuclear factor kappa-light-chain-enhancer of activated B cells), a protein complex involved in the transcription of DNA.
antineoplastic agentA substance that inhibits or prevents the proliferation of neoplasms.
apoptosis inducerAny substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
radiation protective agentAny compound that is able to protect normal cells from the damage caused by radiation therapy.
anti-inflammatory agentAny compound that has anti-inflammatory effects.
bone density conservation agentAn agent that inhibits bone resorption and/or favor bone mineralization and bone regeneration. Used to heal bone fractures and to treat bone diseases such as osteopenia and osteoporosis.
[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 (2)

ClassDescription
tocotrienolA tocol in which the hydrocarbon chain at position 2 contains three double bonds.
vitamin EAny member of a group of fat-soluble chromanols that exhibit biological activity against vitamin E deficiency. The vitamers in this class consists of a chroman-6-ol core which is substituted at position 2 by a methyl group and (also at position 2) either a saturated or a triply-unsaturated hydrocarbon chain consisting of three isoprenoid units. The major function of vitamin E is to act as a natural antioxidant by scavenging free radicals and molecular oxygen.
[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)

PathwayProteinsCompounds
vitamin E biosynthesis (tocotrienols)113

Bioassays (47)

Assay IDTitleYearJournalArticle
AID457739Antiproliferative activity against human MCF7 cells after 96 hrs by MTT assay2010Bioorganic & medicinal chemistry, Jan-15, Volume: 18, Issue:2
Design and preliminary structure-activity relationship of redox-silent semisynthetic tocotrienol analogues as inhibitors for breast cancer proliferation and invasion.
AID327671Antiproliferative activity against mouse +SA mammary epithelial cells after 4 days by MTT assay2008Journal of natural products, Jan, Volume: 71, Issue:1
Semisynthetic and biotransformation studies of (1S,2E,4S,6R,7E,11E)-2,7,11-cembratriene-4,6-diol.
AID1605744Agonist activity at LXR-beta (unknown origin) at 10 uM by coactivator recruitment based Alpha-screen assay2020Journal of medicinal chemistry, 04-09, Volume: 63, Issue:7
Garcinoic Acid Is a Natural and Selective Agonist of Pregnane X Receptor.
AID1662279Metabolic stability in mouse live microsomes assessed as compound degradation in absence of NADPH2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID194999Compound is evaluated for the inhibition of cholesterol biosynthesis in isolated rat hepatocytes at the concentration 250 (ug/mL)1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID194996Inhibitory concentration required to inhibit cholesterol synthesis in isolated rat Hepatocytes1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID1662266Tmax in CD2F1 mouse at 200 mg/kg, sc measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID1662267Cmax in CD2F1 mouse at 200 mg/kg, sc measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID366535Antiproliferative activity against mouse +SA cells assessed as cell viability after 4 days by MTT assay2008Journal of natural products, Aug, Volume: 71, Issue:8
Sinulodurins A and B, antiproliferative and anti-invasive diterpenes from the soft coral Sinularia dura.
AID195000Compound is evaluated for the inhibition of cholesterol biosynthesis in isolated rat hepatocytes at the concentration 500 (ug/mL)1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID1662265AUC (0 to last) in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID194998Compound is evaluated for the inhibition of cholesterol biosynthesis in isolated rat hepatocytes at the concentration 125 (ug/mL)1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID690597Antioxidant activity assessed as ferric ion reducing power by FRAP method2011Bioorganic & medicinal chemistry, Nov-01, Volume: 19, Issue:21
Tocotrienamines and tocopheramines: reactions with radicals and metal ions.
AID1662269Intrinsic clearance in mouse liver microsomes2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID50641picomoles of mevalonic acid synthesized per minute per mg of microsomal protein1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID457738Antiproliferative activity against human MDA-MB-231 cells after 96 hrs by MTT assay2010Bioorganic & medicinal chemistry, Jan-15, Volume: 18, Issue:2
Design and preliminary structure-activity relationship of redox-silent semisynthetic tocotrienol analogues as inhibitors for breast cancer proliferation and invasion.
AID1612323Antiproliferative activity against human A2780 cells assessed as reduction in cell viability incubated for 48 hrs by Alamar blue assay2019Journal of natural products, 03-22, Volume: 82, Issue:3
Phloroglucinols from the Roots of Garcinia dauphinensis and Their Antiproliferative and Antiplasmodial Activities.
AID51430Compound is evaluated for the effect on lipid metabolism in 6-week-old male chickens at a concentration of 20 ppm in the diet and measured for total cholesterol1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID1662268AUC (0 to last) in CD2F1 mouse at 200 mg/kg, sc measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID1662271Metabolic stability in mouse liver microsomes assessed as compound degradation at 1 uM preincubated for 30 mins followed by NADPH addition measured up to 30 mins by HPLC-UV analysis2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID1605741Agonist activity at His-tagged PXR-LBD/SRC-1p (unknown origin) expressed in Escherichia coli BL21(DE3) at 10 uM by coactivator recruitment based Alpha-screen assay2020Journal of medicinal chemistry, 04-09, Volume: 63, Issue:7
Garcinoic Acid Is a Natural and Selective Agonist of Pregnane X Receptor.
AID1662273Volume of distribution in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID745932Antimigratory activity against human MDA-MB-231 cells after 24 hrs by wound-healing assay2013European journal of medicinal chemistry, Jan, Volume: 59Optimization of tocotrienols as antiproliferative and antimigratory leads.
AID50632Compound is evaluated for the effect on lipid metabolism in 6-week-old male chickens at a concentration of 20 ppm in the diet and measured for HDL cholesterol1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID1662274Equlibrium constant in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID1662275AUC (0 to infinity) in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID537457Cytotoxicity against mouse +SA cells after 24 hrs by MTT assay2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Redox-silent tocotrienol esters as breast cancer proliferation and migration inhibitors.
AID1662277Induction of G-CSF production in CD2F1 mouse at 200 mg/kg, sc by G-CSF ELISA kit method2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID1662270Half life in mouse liver microsomes2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID86698Compound evaluated for Percent inhibition of cholesterol synthesis from HMG-CoA Reductase in HepG2 cell1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID1662272Clearance in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID1612324Antiplasmodial activity against Plasmodium falciparum Dd2 assessed as reduction in parasite viability incubated for 72 hrs by SYBR Green I dye based assay2019Journal of natural products, 03-22, Volume: 82, Issue:3
Phloroglucinols from the Roots of Garcinia dauphinensis and Their Antiproliferative and Antiplasmodial Activities.
AID1662278Induction of G-CSF production in CD2F1 mouse at 200 mg/kg, sc pretreated with ketoconazole after 24 hrs by G-CSF ELISA kit method2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID422002Antiinflammatory activity in human neutrophils assessed as inhibition of fMet-Leu-Phe/Cytochalasin B-induced elastase release treated 5 mins before fMet-Leu-Phe/Cytochalasin B challenge2009Journal of natural products, Feb-27, Volume: 72, Issue:2
Benzophenone derivatives from the fruits of Garcinia multiflora and their anti-inflammatory activity.
AID422001Antiinflammatory activity in human neutrophils assessed as inhibition of fMet-Leu-Phe/Cytochalasin B-induced superoxide anion generation treated 5 mins before fMet-Leu-Phe/Cytochalasin B challenge by spectrophotometry2009Journal of natural products, Feb-27, Volume: 72, Issue:2
Benzophenone derivatives from the fruits of Garcinia multiflora and their anti-inflammatory activity.
AID690612Antioxidant activity assessed as ABTS+ free radical scavenging activity by TEAC assay2011Bioorganic & medicinal chemistry, Nov-01, Volume: 19, Issue:21
Tocotrienamines and tocopheramines: reactions with radicals and metal ions.
AID1662276Plasma concentration in CD2F1 mouse at 200 mg/kg, sc administered as single dose measured after 1 hr by HPLC-fluorescence analysis2020Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11
Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production.
AID86699Compound evaluated for Percent inhibition of cholesterol synthesis from [14C]acetate in HepG2 cell1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID690600Antioxidant activity assessed as DPPH free radical scavenging activity2011Bioorganic & medicinal chemistry, Nov-01, Volume: 19, Issue:21
Tocotrienamines and tocopheramines: reactions with radicals and metal ions.
AID50653Compound is evaluated for the effect on lipid metabolism in 6-week-old male chickens at a concentration of 20 ppm in the diet and measured for LDL cholesterol1992Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20
Hypocholesterolemic activity of synthetic and natural tocotrienols.
AID1605748Binding affinity to His-tagged PXR-LBD (unknown origin) expressed in Escherichia coli BL21 Gold at 60 uM by ITC analysis2020Journal of medicinal chemistry, 04-09, Volume: 63, Issue:7
Garcinoic Acid Is a Natural and Selective Agonist of Pregnane X Receptor.
AID277824Inhibition of alpha-glucosidase in 1.20 mg/200 uL2007Journal of natural products, Feb, Volume: 70, Issue:2
Cinnamacrins A-C, cinnafragrin D, and cytostatic metabolites with alpha-glucosidase inhibitory activity from Cinnamosma macrocarpa.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (158)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's9 (5.70)18.2507
2000's26 (16.46)29.6817
2010's89 (56.33)24.3611
2020's34 (21.52)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 28.71

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index28.71 (24.57)
Research Supply Index5.16 (2.92)
Research Growth Index5.11 (4.65)
Search Engine Demand Index70.16 (26.88)
Search Engine Supply Index3.96 (0.95)

This Compound (28.71)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials12 (7.41%)5.53%
Reviews2 (1.23%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other148 (91.36%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]