CHEBI:141698 - L,L-homocystine

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ChEBI Name L,L-homocystine
ChEBI ID CHEBI:141698
ChEBI ASCII Name L,L-homocystine
Definition A homocystine in which both chiral centres have L configuration.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C8H16N2O4S2
Net Charge 0
Average Mass 268.356
Monoisotopic Mass 268.05515
InChI InChI=1S/C8H16N2O4S2/c9-5(7(11)12)1-3-15-16-4-2-6(10)8(13)14/h5-6H,1-4,9-10H2,(H,11,12)(H,13,14)/t5-,6-/m0/s1
InChIKey ZTVZLYBCZNMWCF-WDSKDSINSA-N
SMILES C([C@H](CCSSCC[C@@H](C(=O)O)N)N)(O)=O
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): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via homocystine )
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ChEBI Ontology
Outgoing L,L-homocystine (CHEBI:141698) has functional parent L-homocysteine (CHEBI:17588)
L,L-homocystine (CHEBI:141698) is a homocystine (CHEBI:17485)
L,L-homocystine (CHEBI:141698) is tautomer of L,L-homocystine zwitterion (CHEBI:140613)
Incoming L,L-homocystine zwitterion (CHEBI:140613) is tautomer of L,L-homocystine (CHEBI:141698)
IUPAC Name
(2S,2'S)-4,4'-dithiobis(2-aminobutanoic acid)
Synonyms Sources
(2S)-2-amino-4-{[(3S)-3-amino-3-carboxypropyl]disulfanyl}butanoic acid ChEBI
(2S,2'S)-4,4'-dithiobis(2-aminobutyric acid) ChEBI
L-4,4'-dithio-bis(2-aminobutanoic acid) ChEBI
L-4,4'-dithio-bis(2-aminobutyric acid) ChEBI
L-4,4'-dithiobis(2-aminobutanoic acid) ChEBI
L-homocystine ChemIDplus
Manual Xrefs Databases
C01817 KEGG COMPOUND
FDB022176 FooDB
HMDB0000676 HMDB
Homocystine Wikipedia
HOMOCYSTINE MetaCyc
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Registry Numbers Types Sources
1728583 Reaxys Registry Number Reaxys
626-72-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12934959 PubMed citation Europe PMC
14980706 PubMed citation Europe PMC
16455044 PubMed citation Europe PMC
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Last Modified
20 August 2018