
(-)-Cystine
L-cystine is the L-enantiomer of the sulfur-containing amino acid cystine. It has a role as an EC 1.2.1.11 (aspartate-semialdehyde dehydrogenase) inhibitor, a flour treatment agent, a mouse metabolite, a Saccharomyces cerevisiae metabolite and a human metabolite. It is a cystine, a non-proteinogenic L-alpha-amino acid and a L-cysteine derivative. It is a conjugate acid of a L-cystine anion. It is an enantiomer of a D-cystine. It is a tautomer of a L-cystine zwitterion. — ChEBI
- IUPAC name
- (2R)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]disulfanyl]propanoic acid
- Molecular formula
- C6H12N2O4S2
- Molecular weight
- 240.3 g/mol
- Exact mass
- 240.02384922 Da
- XLogP3
- -6.3
- Topological polar surface area
- 177.0 Ų
- Hydrogen-bond donors
- 4
- Hydrogen-bond acceptors
- 8
- Covalent units
- 1
- Defined stereocentres
- 2
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:16283
- ChEMBL:CHEMBL590540
- EPA DTXSID:DTXSID2046418
- PubMed:35204234
- PubMed:22675475
- PubMed:22561356
- PubMed:22548128
- PubMed:22291693
- PubMed:22230336
- PubMed:22216172
- PubMed:22145046
- PubMed:22093698
- PubMed:21801426
- PubMed:21714924
- PubMed:21699715
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.