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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
Control of cytochrome C redox potential: axial ligation and protein environment effects.
2002 May 15
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
Temperature dependence of the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2003 Oct 1
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: functional studies of the promiscuous o-succinylbenzoate synthase from Amycolatopsis.
2004 Jan 13
Molecular cloning and biochemical characterization of L-N-carbamoylase from Sinorhizobium meliloti CECT4114.
2005
Methionine radical cation: structural studies as a function of pH using X- and Q-band time-resolved electron paramagnetic resonance spectroscopy.
2005 Jul 7
Purification and characterization of a novel aminoacylase from Streptomyces mobaraensis.
2005 Oct
In vivo metabolism of L-methionine in mice: evidence for stereoselective formation of methionine-d-sulfoxide and quantitation of other major metabolites.
2006 Dec
Probing the catalytic center of porcine aminoacylase 1 by site-directed mutagenesis, homology modeling and substrate docking.
2006 Mar
Characterization of a bifunctional aminoacylase/carboxypeptidase from radioresistant bacterium Deinococcus radiodurans R1.
2007 Feb 1
The role of N-acetyl-methioninate as a new stabilizer for albumin products.
2007 Feb 1
X-ray spectroscopic approaches to the investigation and characterization of photochemical processes.
2009 Jul
A bulky platinum triamine complex that reacts faster with guanosine 5'-monophosphate than with N-acetylmethionine.
2010 Feb
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 Mon Mar 31 17:47:34 GMT 2025
Edited
by admin
on Mon Mar 31 17:47:34 GMT 2025
Record UNII
9J12WX5B6A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-ACETYLMETHIONINE
MI  
Systematic Name English
ACETYL METHIONINE
INCI  
INCI  
Preferred Name English
METHIONIN
Systematic Name English
Acetylmethionine [WHO-DD]
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
METHIONAMINE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.372
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
Code System Code Type Description
NSC
118514
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
PUBCHEM
448580
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
SMS_ID
100000077932
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-617-7
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
CAS
65-82-7
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
DRUG BANK
DB01646
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
MERCK INDEX
m1362
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY Merck Index
EVMPD
SUB12722MIG
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
RXCUI
1426463
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY RxNorm
MESH
C006379
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
CHEBI
16811
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID00883214
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
DAILYMED
9J12WX5B6A
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
CHEBI
21557
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
FDA UNII
9J12WX5B6A
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
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