Page last updated: 2024-12-09

o-methyl threonine

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

Description

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

O-methyl-L-threonine : An L-threonine derivative that is L-threonine with a methyl group replacing the hydrogen on the hydroxy side chain. [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 CID2724875
CHEMBL ID1234983
CHEBI ID44514
SCHEMBL ID304488
MeSH IDM0042890

Synonyms (38)

Synonym
4144-02-9
CHEMBL1234983
o-methyl-l-threonine
threonine, o-methyl-
o-methyl-threonine
B46A3F30-8EE8-4747-B95C-D18E65102610
o-methyl threonine
(2s,3r)-2-amino-3-methoxybutanoic acid
4385-90-4
AKOS006237897
l-threonine methyl ether
h-thr(me)-oh
2076-57-5
SCHEMBL304488
AM82265
FYCWLJLGIAUCCL-DMTCNVIQSA-N
(2s,3r)-2-amino-3-methoxy-butanoic acid
o-methylthreonine
unii-oai4pjx6xs
l-threonine, o-methyl-
OAI4PJX6XS ,
butyric acid, 2-amino-3-methoxy-, l-
CS-W008464
mfcd00037767
DTXSID20195962
threonine, o-methyl- (9ci)
DS-13964
Q27285544
l-o-methylthreonine
CHEBI:44514
(2s,3r)-2-amino-3-methoxybutyric acid
EN300-312324
(2s,3r)-2-amino-3-methoxybutanoicacid
DTXSID701031342
o-methyl-dl-threonine
HY-W008464
l-thr(me)-oh
(s)-2-amino-3-methoxybutanoic acid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
bleaching agentA reagent that lightens or whitens a substrate through chemical reaction. Bleaching reactions usually involve oxidative or reductive processes that degrade colour systems. Bleaching can occur by destroying one or more of the double bonds in the conjugated chain, by cleaving the conjugated chain, or by oxidation of one of the other moieties in the conjugated chain. Their reactivity results in many bleaches having strong bactericidal, disinfecting, and sterilising properties.
antibacterial agentA substance (or active part thereof) that kills or slows the growth of bacteria.
[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 (3)

ClassDescription
non-proteinogenic L-alpha-amino acidAny L-alpha-amino acid which is not a member of the group of 23 proteinogenic amino acids.
L-threonine derivativeA proteinogenic amino acid derivative resulting from reaction of L-threonine at the amino group or the carboxy group, or from the replacement of any hydrogen of L-threonine by a heteroatom.
etherAn organooxygen compound with formula ROR, where R is not hydrogen.
[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]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1136834Antimalarial activity against Plasmodium berghei infected in mouse assessed as increase of survival time of host at 160 to 640 mg/kg1979Journal of medicinal chemistry, Jul, Volume: 22, Issue:7
Dipeptides of O-methyl-L-threonine as potential antimalarials.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.66

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.66 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.45 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.66)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]