Page last updated: 2024-12-04

methionine sulfoxide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

methionine sulfoxide: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

L-methionine (R)-S-oxide : The (R)-oxido diastereomer of L-methionine S-oxide. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID10062737
CHEBI ID49032
SCHEMBL ID689456
MeSH IDM0060627

Synonyms (13)

Synonym
methionine sulfoxide
l-methionine (r)-s-oxide
(2s)-2-amino-4-[(r)-methylsulfinyl]butanoic acid
CHEBI:49032
DB02235
SME ,
3226-66-2
SCHEMBL689456
methionine-r-sulfoxide
Q27093276
2-azaniumyl-4-methylsulfinylbutanoate
(2s)-2-amino-4-[(r)-methanesulfinyl]butanoic acid
EN300-26934398

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" An additional consideration for determining methionine and cysteine bioavailability is that not all dietary methionine and cysteine is digested and absorbed from the small intestine."( Determination of sulfur amino acids in foods as related to bioavailability.
Moughan, PJ; Rutherfurd, SM,
)
0.13

Dosage Studied

ExcerptRelevanceReference
" Vitamin U and its major degradation product in the dosage forms, viz."( Determination of vitamin U and its degradation products by high- performance liquid chromatography with fluorescence detection.
Leung, CP; Leung, WK, 1989
)
0.28
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
L-methionine S-oxide
amino acid zwitterionThe zwitterionic form of an amino acid having a negatively charged carboxyl group and a positively charged amino group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (2)

PathwayProteinsCompounds
Metabolism of proteins1058144
Protein repair39

Research

Studies (329)

TimeframeStudies, This Drug (%)All Drugs %
pre-199053 (16.11)18.7374
1990's44 (13.37)18.2507
2000's96 (29.18)29.6817
2010's113 (34.35)24.3611
2020's23 (6.99)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials4 (1.16%)5.53%
Reviews30 (8.72%)6.00%
Case Studies2 (0.58%)4.05%
Observational3 (0.87%)0.25%
Other305 (88.66%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]