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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
Release of alpha-melanocyte stimulating hormone into rat and human cerebrospinal fluid in vivo and from rat hypothalamus slices in vitro.
1981 Spring
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
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SUPERSEDED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SUPERSEDED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