Page last updated: 2024-11-08

thiocysteine

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

Description

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

3-disulfanyl-L-alanine : An S-substituted L-cysteine where the S-substituent is specified as sulfanyl. [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 CID165331
CHEBI ID28839
MeSH IDM0167331

Synonyms (32)

Synonym
CHEBI:28839
3-disulfanyl-l-alanine
2-amino-3-persulfhydrylpropanoic acid
2-amino-3-hydropersulfidopropanoic acid
(r)-2-amino-3-disulfanylpropanoic acid
s-sulfanylcysteine
3-(thiosulfeno)-alanine
2-amino-3-hydrodisulfidopropanoic acid
cysteine persulfide
2-amino-3-disulfanylpropanoic acid
cysteine perthiol
6165-31-7
s-mercaptocysteine
CSS ,
s-mercapto-l-cysteine
C01962
5652-32-4
thiocysteine ,
DB02761
(2r)-2-amino-3-(disulfanyl)propanoic acid
alanine, 3-(thiosulfeno)-
unii-3rz74wa9j2
DTXSID00205073
s-thiocystine
l-alanine, 3-(thiosulfeno)-
3-(thiosulfeno)-l-alanine
3RZ74WA9J2 ,
3-(thiosulfeno)alanine
l-cysteine persulfide
Q27093709
HY-115890
CS-0375613
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[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
amino acid zwitterionThe zwitterionic form of an amino acid having a negatively charged carboxyl group and a positively charged amino group.
S-substituted L-cysteine
[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
Methionine and Cysteine metabolism ( Methionine and Cysteine metabolism )2342

Research

Studies (36)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.78)18.7374
1990's2 (5.56)18.2507
2000's6 (16.67)29.6817
2010's24 (66.67)24.3611
2020's3 (8.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 22.33

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 Index22.33 (24.57)
Research Supply Index3.61 (2.92)
Research Growth Index5.35 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.33)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews9 (25.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other27 (75.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]