CHEBI:16375 - D-cysteine

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name D-cysteine ChEBI ID CHEBI:16375 ChEBI ASCII Name D-cysteine Definition An optically active form of cysteine having D-configuration. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:4111, CHEBI:41887, CHEBI:12919, CHEBI:20921 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C3H7NO2S Net Charge 0 Average Mass 121.15922 Monoisotopic Mass 121.01975 InChI InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1 InChIKey XUJNEKJLAYXESH-UWTATZPHSA-N SMILES N[C@H](CS)C(O)=O Metabolite of Species Details Escherichia coli (NCBI:txid562) See: PubMed Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Biological Role(s): fundamental metabolite Any metabolite produced by all living cells. (via cysteine ) View more via ChEBI Ontology ChEBI Ontology Outgoing D-cysteine (CHEBI:16375) is a D-α-amino acid (CHEBI:16733) D-cysteine (CHEBI:16375) is a cysteine (CHEBI:15356) D-cysteine (CHEBI:16375) is conjugate acid of D-cysteinate(1−) (CHEBI:32449) D-cysteine (CHEBI:16375) is conjugate base of D-cysteinium (CHEBI:32451) D-cysteine (CHEBI:16375) is enantiomer of L-cysteine (CHEBI:17561) D-cysteine (CHEBI:16375) is tautomer of D-cysteine zwitterion (CHEBI:35236) Incoming D-cysteine derivative (CHEBI:83835) has functional parent D-cysteine (CHEBI:16375) D-cysteinyl radical (CHEBI:32738) has functional parent D-cysteine (CHEBI:16375) D-cysteinium (CHEBI:32451) is conjugate acid of D-cysteine (CHEBI:16375) D-cysteinate(1−) (CHEBI:32449) is conjugate base of D-cysteine (CHEBI:16375) L-cysteine (CHEBI:17561) is enantiomer of D-cysteine (CHEBI:16375) D-cystein-S-yl group (CHEBI:32794) is substituent group from D-cysteine (CHEBI:16375) D-cysteine residue (CHEBI:29951) is substituent group from D-cysteine (CHEBI:16375) D-cysteinyl group (CHEBI:32452) is substituent group from D-cysteine (CHEBI:16375) D-cysteine zwitterion (CHEBI:35236) is tautomer of D-cysteine (CHEBI:16375) IUPAC Name D-cysteine Synonyms Sources (2S)-2-amino-3-mercaptopropanoic acid JCBN (2S)-2-amino-3-sulfanylpropanoic acid IUPAC (S)-2-amino-3-mercaptopropanoic acid ChEBI D-Amino-3-mercaptopropionic acid KEGG COMPOUND D-Cystein ChEBI D-CYSTEINE PDBeChem D-Cysteine KEGG COMPOUND D-Zystein ChEBI DCY PDBeChem Manual Xrefs Databases C00007323 KNApSAcK C00793 KEGG COMPOUND DB03201 DrugBank DCY PDBeChem ECMDB03417 ECMDB HMDB0003417 HMDB YMDB00913 YMDB View more database links Registry Numbers Types Sources 1721407 Reaxys Registry Number Reaxys 1721407 Beilstein Registry Number Beilstein 363236 Gmelin Registry Number Gmelin 921-01-7 CAS Registry Number KEGG COMPOUND 921-01-7 CAS Registry Number ChemIDplus Citations Types Sources 13761469 PubMed citation Europe PMC 23340406 PubMed citation Europe PMC 24800864 PubMed citation Europe PMC Last Modified 25 January 2016