Basic information
- CAS
14172-54-4- Standard SMILES
N[C@@H](CSSSC[C@H](N)C(=O)O)C(=O)O- InChIKey
NPDOQLBQFXZAJD-BKLSDQPFSA-N- Molecular formula
- C6H12N2O4S3
- Average molar mass
- 272.4 g/mol
- Monoisotopic mass
- 271.99592039
Overview
Bis(2-amino-2-carboxyethyl)trisulfide has been reported in Escherichia coli with data available.
Names & identifiers
- Preferred name
- Thiocystine
- IUPAC
- (2R)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]trisulfanyl]propanoic acid
- English name
- thiocystine
- Molecular formula
- C6H12N2O4S3
- Molecular weight
- 0
Names & synonyms
Bis(2-amino-2-carboxyethyl)trisulfideThiocystine14172-54-4(2R)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]trisulfanyl]propanoic acid(2R)-2-amino-3-(((2R)-2-amino-2-carboxyethyl)trisulfanyl)propanoic acidRefChem:189499Cystine trisulfide15807-59-7Alanine, 3,3'-trithiobis-QTJ7UB3UX83,3'-Trithiobis[L-alanine]SCHEMBL12390074
Show more names
3,3'-bis(cysteine) trisulfide
Alanine, 3,3'-trithiodi-, L-Alanine, 3,3'-trithiodi-, L- (8CI); 3,3'-Trithiobis[L-alanine]; (2R,2'R)-3,3'-trisulfanediylbis(2-aminopropanoic acid)
Database identifiers
- CAS
14172-54-4、15807-59-7- PubChem CID
- 167019
- UNII
- QTJ7UB3UX8
- Nikkaji
- J1.066.174I
Properties
Computed structural properties
- XLogP
- -5.8
- Topological polar surface area
- 203 Ų
- Hydrogen bond donors
- 4
- Hydrogen bond acceptors
- 9
- Rotatable bonds
- 8
- Heavy atoms
- 15
- Formal charge
- 0
- Complexity
- 206
Chemistry & industry
Applications
DescriptionThiocystine is produced in the hydrolysis of proteins.
UsesThiocystine is a relatively stable trisulfide analog of Cystine. Thiocystine functions as a persullide in transferring its sulfane sulfur to thiophilic acceptors[1][2].
Suppliers2 total
杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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