CHEBI:156139 - N-acetyl-L-thialysine

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ChEBI Name N-acetyl-L-thialysine
ChEBI ID CHEBI:156139
ChEBI ASCII Name N-acetyl-L-thialysine
Definition An L-cysteine thioether resulting from the formal condensation of the carboxy group of acetic acid with the amino group of L-thialysine.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C7H14N2O3S
Net Charge 0
Average Mass 206.260
Monoisotopic Mass 206.07251
InChI InChI=1S/C7H14N2O3S/c1-5(10)9-2-3-13-4-6(8)7(11)12/h6H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t6-/m0/s1
InChIKey NTYDEVWJGFRRKF-LURJTMIESA-N
SMILES OC([C@H](CSCCNC(C)=O)N)=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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-acetyl-L-thialysine (CHEBI:156139) has functional parent L-thialysine (CHEBI:497734)
N-acetyl-L-thialysine (CHEBI:156139) is a L-cysteine thioether (CHEBI:27532)
N-acetyl-L-thialysine (CHEBI:156139) is a acetamides (CHEBI:22160)
N-acetyl-L-thialysine (CHEBI:156139) is tautomer of N-acetyl-L-thialysine zwitterion (CHEBI:156134)
Incoming N-acetyl-L-thialysine zwitterion (CHEBI:156134) is tautomer of N-acetyl-L-thialysine (CHEBI:156139)
IUPAC Name
S-(2-acetamidoethyl)-L-cysteine
Synonyms Sources
(2R)-3-[(2-acetamidoethyl)sulfanyl]-2-aminopropanoic acid IUPAC
ε-N-acetyl-L-thialysine ChEBI
epsilon-N-acetylthialysine ChEBI
ε-N-acetylthialysine ChemIDplus
N-acetyl-L-thialysine ChEBI
S-(2-N-acetylaminoethyl)-L-cysteine ChEBI
Registry Number Type Source
20662-33-3 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
121995 PubMed citation Europe PMC
Last Modified
14 July 2020