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Details

Stereochemistry MIXED
Molecular Formula C5H11NO3S
Molecular Weight 165.211
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHIONINE SULFOXIDE, DL-

SMILES

C[S+]([O-])CCC(N)C(O)=O

InChI

InChIKey=QEFRNWWLZKMPFJ-UHFFFAOYSA-N
InChI=1S/C5H11NO3S/c1-10(9)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)

HIDE SMILES / InChI

Molecular Formula C5H11NO3S
Molecular Weight 165.211
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of neutrophil cathepsin G by oxidized mucus proteinase inhibitor. Effect of heparin.
1999 Jun 29
Simultaneous determination of methionine sulfoxide and methionine in blood plasma using gas chromatography-mass spectrometry.
2003 Feb 1
Functioning methionine-S-sulfoxide reductases A and B are present in human skin.
2006 May
Protection of vascular smooth muscle cells by over-expressed methionine sulphoxide reductase A: role of intracellular localization and substrate availability.
2008 Nov
Potential for development of an Escherichia coli-based biosensor for assessing bioavailable methionine: a review.
2010
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:38:44 GMT 2023
Edited
by admin
on Fri Dec 15 20:38:44 GMT 2023
Record UNII
O74B4F6OYL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHIONINE SULFOXIDE, DL-
Common Name English
BUTANOIC ACID, 2-AMINO-4-(METHYLSULFINYL)-
Common Name English
BUTYRIC ACID, .ALPHA.-AMINO-.GAMMA.-(METHYLSULFINYL)-
Common Name English
2-AMINO-4-(METHYLSULPHINYL)BUTYRIC ACID
Systematic Name English
2-AMINO-4-(METHYLSULFINYL)BUTANOIC ACID
Systematic Name English
NSC-3084
Code English
DL-METHIONINE SULFOXIDE
Common Name English
UETHIONINE, S-OXIDE
Common Name English
BUTANOIC ACID, 2-AMINO-4-(METHYLSULFINYL)-, (±)-
Common Name English
Code System Code Type Description
NSC
3084
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
263-700-7
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY
CAS
4241-59-2
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
SUPERSEDED
CAS
454-41-1
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
SUPERSEDED
FDA UNII
O74B4F6OYL
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID60866947
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY
PUBCHEM
847
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY
CAS
62697-73-8
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-225-5
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
ALTERNATIVE
CHEBI
49033
Created by admin on Fri Dec 15 20:38:44 GMT 2023 , Edited by admin on Fri Dec 15 20:38:44 GMT 2023
PRIMARY