CHEBI:134543 - (R)-4-hydroxy-1-methyl-L-proline

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ChEBI Name (R)-4-hydroxy-1-methyl-L-proline
ChEBI ASCII Name (R)-4-hydroxy-1-methyl-L-proline
Definition An L-proline derivative that is trans-4-hydroxy-L-proline in which the amino hydrogen has been replaced by a methyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H11NO3
Net Charge 0
Average Mass 145.157
Monoisotopic Mass 145.07389
InChI InChI=1S/C6H11NO3/c1-7-3-4(8)2-5(7)6(9)10/h4-5,8H,2-3H2,1H3,(H,9,10)/t4-,5+/m1/s1
Metabolite of Species Details
Dalbergia sympathetica (IPNI:490488-1) Found in leaf (BTO:0000713). See: PubMed
Aglaia andamanica (IPNI:576960-1) Found in leaf (BTO:0000713). See: PubMed
Arabidopsis thaliana (NCBI:txid3702) See: MetaboLights Study
Psittacanthus calyculatus (NCBI:txid529590) Found in whole plant (BTO:0001461). See: PubMed
Ipomoea carnea (NCBI:txid89640) Found in leaf (BTO:0000713). See: PubMed
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
anti-HIV-1 agent
An anti-HIV agent that destroys or inhibits the replication of HIV-1, the more infective and more virulent of the two types of HIV virus.
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (R)-4-hydroxy-1-methyl-L-proline (CHEBI:134543) has functional parent trans-4-hydroxy-L-proline (CHEBI:18095)
(R)-4-hydroxy-1-methyl-L-proline (CHEBI:134543) has role anti-HIV-1 agent (CHEBI:64947)
(R)-4-hydroxy-1-methyl-L-proline (CHEBI:134543) has role plant metabolite (CHEBI:76924)
(R)-4-hydroxy-1-methyl-L-proline (CHEBI:134543) is a L-proline derivative (CHEBI:84186)
(R)-4-hydroxy-1-methyl-L-proline (CHEBI:134543) is a pyrrolidine alkaloid (CHEBI:26456)
Synonyms Sources
(4R)-4-hydroxy-1-methyl-L-proline ChEBI
(R)-4-hydroxy-1-methylproline ChEBI
(R)-4-hydroxy-N-methyl-L-proline ChEBI
(R)-4-hydroxy-N-methylproline ChEBI
N-methyl-trans-4-hydroxy-L-proline ChEBI
Manual Xref Database
9943383 ChemSpider
View more database links
Registry Number Type Source
472151 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11199132 PubMed citation Europe PMC
12903959 PubMed citation Europe PMC
16425210 PubMed citation Europe PMC
22071447 PubMed citation Europe PMC
26427611 PubMed citation Europe PMC
Last Modified
06 July 2017