Page last updated: 2024-12-06

s-methylcysteine

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

Description

S-methylcysteine: RN given refers to parent cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

S-methylcysteine : A cysteine derivative that is L-cysteine in which the hydrogen attached to the sulfur is replaced by a methyl 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]

Cross-References

ID SourceID
PubMed CID24417
CHEMBL ID394875
CHEBI ID45658
SCHEMBL ID110458
MeSH IDM0052265

Synonyms (58)

Synonym
1187-84-4
nsc-15387
l-cysteine, s-methyl-
s-methylcysteine
s-methyl-l-cysteine ,
alanine, 3-(methylthio)-, l-
s-methyl-l-cysteine, substrate for methionine sulfoxide reductase a
DB02216
einecs 214-701-6
nsc 15387
ccris 1972
M-3585
0DDF4489-1BF1-4858-9127-80A71A348EC8
chebi:45658 ,
CHEMBL394875 ,
AKOS000275785
(2r)-2-amino-3-methylsulfanylpropanoic acid
(r)-2-amino-3-(methylthio)propanoic acid
bdbm50213729
M0233
h-cys(me)-oh
A804094
einecs 243-203-1
s-methyl-dl-cysteine
unii-a34i1h07ym
a34i1h07ym ,
(r)-2-amino-3-(methylmercapto)propionic acid
3-(methylthio)-l-alanine
(2r)-2-amino-3-(methylsulfanyl)propanoic acid
l-methylcysteine
S4786
s-methyl-l-cysteine, (-)-
3-(methylthio)alanine
s-methyl-(r)-cysteine
s-methylcysteine, l-
SCHEMBL110458
AM82581
l-s-methyl-cysteine
l-ch3sch2ch(nh2)cooh
(-)-s-methyl-l-cysteine
J-300343
s-methyl-cysteine
methylcysteine
CS-7653
mfcd00002612
GS-3468
s-methyl-l-cys
HY-B2188
d-s-methyl-cysteine
DTXSID50862579
Z760035320
Q27093260
C22040
h-cys(me)-oh.hcl
CCG-266126
cysteine,s-methyl-
s-n-methylcysteine
EN300-314842

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" Methylmercapturic acid and N-(methylthioacetyl)glycine have been isolated from the urine of the dosed animals."( BIOCHEMICAL STUDIES OF TOXIC AGENTS. THE METABOLISM OF IODOMETHANE.
BARNSLEY, EA; YOUNG, L, 1965
)
0.24
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
human urinary metaboliteAny metabolite (endogenous or exogenous) found in human urine samples.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[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
S-alkyl-L-cysteine
S-alkyl-L-cysteine zwitterionAn S-substituted L-cysteine zwitterion in which the S-substituent can be any alkyl group.
[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]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Kinesin-like protein KIF11Homo sapiens (human)IC50 (µMol)63.00000.00011.405710.0000AID299460
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (9)

Processvia Protein(s)Taxonomy
mitotic cell cycleKinesin-like protein KIF11Homo sapiens (human)
microtubule-based movementKinesin-like protein KIF11Homo sapiens (human)
spindle organizationKinesin-like protein KIF11Homo sapiens (human)
mitotic spindle organizationKinesin-like protein KIF11Homo sapiens (human)
mitotic centrosome separationKinesin-like protein KIF11Homo sapiens (human)
regulation of mitotic centrosome separationKinesin-like protein KIF11Homo sapiens (human)
cell divisionKinesin-like protein KIF11Homo sapiens (human)
mitotic spindle assemblyKinesin-like protein KIF11Homo sapiens (human)
spindle elongationKinesin-like protein KIF11Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (6)

Processvia Protein(s)Taxonomy
microtubule motor activityKinesin-like protein KIF11Homo sapiens (human)
protein bindingKinesin-like protein KIF11Homo sapiens (human)
ATP bindingKinesin-like protein KIF11Homo sapiens (human)
microtubule bindingKinesin-like protein KIF11Homo sapiens (human)
protein kinase bindingKinesin-like protein KIF11Homo sapiens (human)
plus-end-directed microtubule motor activityKinesin-like protein KIF11Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (10)

Processvia Protein(s)Taxonomy
spindle poleKinesin-like protein KIF11Homo sapiens (human)
spindle microtubuleKinesin-like protein KIF11Homo sapiens (human)
spindleKinesin-like protein KIF11Homo sapiens (human)
cytosolKinesin-like protein KIF11Homo sapiens (human)
microtubuleKinesin-like protein KIF11Homo sapiens (human)
membraneKinesin-like protein KIF11Homo sapiens (human)
mitotic spindleKinesin-like protein KIF11Homo sapiens (human)
kinesin complexKinesin-like protein KIF11Homo sapiens (human)
protein-containing complexKinesin-like protein KIF11Homo sapiens (human)
nucleusKinesin-like protein KIF11Homo sapiens (human)
mitotic spindleKinesin-like protein KIF11Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID299460Inhibition of Eg5 assessed as inhibition ATP hydrolysis by ATPase assay2007Bioorganic & medicinal chemistry letters, Jul-15, Volume: 17, Issue:14
Synthesis and biological evaluation of L-cysteine derivatives as mitotic kinesin Eg5 inhibitors.
AID299461Cytotoxic activity against HeLa cells2007Bioorganic & medicinal chemistry letters, Jul-15, Volume: 17, Issue:14
Synthesis and biological evaluation of L-cysteine derivatives as mitotic kinesin Eg5 inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (96)

TimeframeStudies, This Drug (%)All Drugs %
pre-199035 (36.46)18.7374
1990's11 (11.46)18.2507
2000's27 (28.13)29.6817
2010's19 (19.79)24.3611
2020's4 (4.17)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 28.85

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 Index28.85 (24.57)
Research Supply Index4.62 (2.92)
Research Growth Index4.53 (4.65)
Search Engine Demand Index36.43 (26.88)
Search Engine Supply Index2.61 (0.95)

This Compound (28.85)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.00%)6.00%
Case Studies2 (2.00%)4.05%
Observational0 (0.00%)0.25%
Other97 (97.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]