CHEBI:132958 - N-acetylmethionine

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ChEBI Name N-acetylmethionine
ChEBI ASCII Name N-acetylmethionine
Definition A methionine derivative that is methionine in which one of the amine hydrogens is substituted by an acetyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:7211
Supplier Information
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Formula C7H13NO3S
Net Charge 0
Average Mass 191.249
InChI InChI=1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)
Roles Classification
Chemical Role(s): 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-acetylmethionine (CHEBI:132958) is a N-acyl-amino acid (CHEBI:51569)
N-acetylmethionine (CHEBI:132958) is a methionine derivative (CHEBI:25230)
N-acetylmethionine (CHEBI:132958) is a methyl sulfide (CHEBI:86315)
N-acetylmethionine (CHEBI:132958) is a monocarboxylic acid (CHEBI:25384)
N-acetylmethionine (CHEBI:132958) is conjugate acid of N-acetylmethioninate (CHEBI:132957)
Incoming N-acetyl-D-methionine (CHEBI:85210) is a N-acetylmethionine (CHEBI:132958)
N-acetyl-L-methionine (CHEBI:21557) is a N-acetylmethionine (CHEBI:132958)
N-acetylmethioninate (CHEBI:132957) is conjugate base of N-acetylmethionine (CHEBI:132958)
Synonyms Sources
2-acetamido-4-(methylsulfanyl)butanoic acid IUPAC
2-acetylamino-4-methylsulfanyl-butyric acid ChEBI
Ac-Met ChEBI
N-Ac-Met ChEBI
Registry Numbers Types Sources
1115-47-5 CAS Registry Number ChemIDplus
1725554 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1157846 PubMed citation Europe PMC
16129491 PubMed citation Europe PMC
23626375 PubMed citation Europe PMC
2738074 PubMed citation Europe PMC
35357105 PubMed citation Europe PMC
448454 PubMed citation Europe PMC
9589603 PubMed citation Europe PMC
Last Modified
12 July 2022
General Comment
2022-07-12 This is the entry for material with unspecified stereochemistry. There are separate entries for the racemate (N-acetyl-DL-methionine) and its individual enantiomers.