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Details

Stereochemistry ABSOLUTE
Molecular Formula C7H13NO3S
Molecular Weight 191.248
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-ACETYLMETHIONINE

SMILES

CSCC[C@H](NC(C)=O)C(O)=O

InChI

InChIKey=XUYPXLNMDZIRQH-LURJTMIESA-N
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)/t6-/m0/s1

HIDE SMILES / InChI

Molecular Formula C7H13NO3S
Molecular Weight 191.248
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Specific enhancement of acylase I and acylpeptide hydrolase activities by the corresponding N-acetylated substrates in primary rat hepatocyte cultures.
2002 Feb
Cystathionine pathway-dependent cytotoxicities of diethyl maleate and diamide in rat and human hepatoma-derived cell cultures.
2002 Jan-Feb
Identification and characterization of a new gene from Variovorax paradoxus Iso1 encoding N-acyl-D-amino acid amidohydrolase responsible for D-amino acid production.
2002 Oct
L-methionine inhibits reaction of DNA with anticancer cis-diamminedichloroplatinum(II).
2002 Sep 10
Importance of product inhibition in the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2002 Sep 15
Kinetic analysis of the reactions of hypobromous acid with protein components: implications for cellular damage and use of 3-bromotyrosine as a marker of oxidative stress.
2004 Apr 27
Effect of amine ligand bulk on the interaction of methionine with platinum(II) diamine complexes.
2004 Feb 9
Evolution of enzymatic activity in the enolase superfamily: structural studies of the promiscuous o-succinylbenzoate synthase from Amycolatopsis.
2004 May 18
Probing the catalytic center of porcine aminoacylase 1 by site-directed mutagenesis, homology modeling and substrate docking.
2006 Mar
X-ray spectroscopic approaches to the investigation and characterization of photochemical processes.
2009 Jul
Formation and hydrolysis of amide bonds by lipase A from Candida antarctica; exceptional features.
2010 Feb 21
Specific reaction of Met 35 in amyloid beta peptide with hypochlorous acid.
2010 Jul
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:08:01 UTC 2023
Edited
by admin
on Fri Dec 15 15:08:01 UTC 2023
Record UNII
9J12WX5B6A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-ACETYLMETHIONINE
MI  
Systematic Name English
METHIONIN
Systematic Name English
Acetylmethionine [WHO-DD]
Common Name English
ACETYL METHIONINE [INCI]
Common Name English
THIOMEDON
Common Name English
ACETYL-L-METHIONINE
Systematic Name English
NSC-118514
Code English
N-ACETYLMETHIONINE [MI]
Common Name English
ACETYLMETHIONINE
WHO-DD  
Systematic Name English
N-ACETYL-L-METHIONINE [FCC]
Common Name English
METHIONINE, N-ACETYL-, L-
Systematic Name English
FOLLICUSAN
Brand Name English
L-(N-ACETYL)METHIONINE
Common Name English
L-METHIONINE, N-ACETYL-
Systematic Name English
N-ACETYL-L-2-AMINO-4-(METHYLTHIO)BUTYRIC ACID
Common Name English
METHIONINE, N-ACETYL-, L
Common Name English
N-ACETYL-L-METHIONINE
FCC  
Systematic Name English
ACETYL METHIONINE
INCI  
INCI  
Official Name English
METHIONAMINE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.372
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
Code System Code Type Description
NSC
118514
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
PUBCHEM
448580
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
SMS_ID
100000077932
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-617-7
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
CAS
65-82-7
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
DRUG BANK
DB01646
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
MERCK INDEX
m1362
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY Merck Index
EVMPD
SUB12722MIG
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
RXCUI
1426463
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY RxNorm
MESH
C006379
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
CHEBI
16811
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
EPA CompTox
DTXSID00883214
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
DAILYMED
9J12WX5B6A
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
CHEBI
21557
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
FDA UNII
9J12WX5B6A
Created by admin on Fri Dec 15 15:08:01 UTC 2023 , Edited by admin on Fri Dec 15 15:08:01 UTC 2023
PRIMARY
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