Page last updated: 2024-11-08

s-(1,2-dicarboxyethyl)cysteine

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

Description

S-(1,2-dicarboxyethyl)cysteine: isolated from a toadstool, Amanita pantherina as a mixture of (2R),(1'R) and (2R),(1'S) diastereomers [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

S-(2-succinyl)-L-cysteine : An L-cysteine thioether that is L-cysteine in which the hydrogen of the thiol group has been replaced by a 1,2-dicarboxyethyl group. It is a chemical modification which occurs in tissue proteins and formed by a Michael addition of cysteine to fumaric acid. [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 CID25060473
CHEBI ID144907
SCHEMBL ID4154758
MeSH IDM0067807

Synonyms (20)

Synonym
2-{[(2r)-2-amino-2-carboxyethyl]sulfanyl}butanedioic acid
s-(2-succinyl)-l-cysteine
2-[[(2r)-2-amino-2-carboxyethyl]thio]butanedioic acid
s-(1,2-dicarboxyethyl)-l-cysteine
CHEBI:144907
s-(2-succino)-l-cysteine
547764-73-8
[[(2r)-2-amino-2-carboxyethyl]thio]succinic acid
s-(1,2-dicarboxyethyl)cysteine
SCHEMBL4154758
s-(2-succinyl)cysteine
AKOS030228785
s-(1,2-dicarboxyethyl)l-cysteine
mfcd31380746
unii-dt9kev171h
butanedioic acid, (((2r)-2-amino-2-carboxyethyl)thio)-
2-(((2r)-2-amino-2-carboxyethyl)thio)butanedioic acid
dt9kev171h ,
2-[(2r)-2-amino-2-carboxyethyl]sulfanylbutanedioic acid
2-(((r)-2-amino-2-carboxyethyl)thio)succinic acid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
Maillard reaction productAny thermal degradation product obtained as a result of a chemical reaction between an amino acid and a reducing sugar (Maillard reaction, a non-enzymatic browning procedure that usually imparts flavour to starch-based food products).
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 (2)

ClassDescription
L-cysteine thioetherAny L-cysteine derivative obtained by conversion of the thiol group into a sulfide.
tricarboxylic acidAn oxoacid containing three carboxy groups.
[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]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (4.55)18.7374
1990's3 (13.64)18.2507
2000's5 (22.73)29.6817
2010's8 (36.36)24.3611
2020's5 (22.73)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (4.35%)4.05%
Observational0 (0.00%)0.25%
Other22 (95.65%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]