CHEBI:90344 - N-methylproline

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ChEBI Name N-methylproline
ChEBI ID CHEBI:90344
ChEBI ASCII Name N-methylproline
Definition An L-proline derivative obtained by replacement of the amino hydrogen by a methyl group.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C6H11NO2
Net Charge 0
Average Mass 129.159
Monoisotopic Mass 129.07898
InChI InChI=1S/C6H11NO2/c1-7-4-2-3-5(7)6(8)9/h5H,2-4H2,1H3,(H,8,9)/t5-/m0/s1
InChIKey CWLQUGTUXBXTLF-YFKPBYRVSA-N
SMILES [C@H]1(CCCN1C)C(O)=O
Metabolite of Species Details
Tamarix jordanis (NCBI:txid1112732) See: PubMed
Castanea sativa (NCBI:txid21020) Found in kernel (BTO:0000668). See: PubMed
Citrus bergamia (NCBI:txid380129) Found in fruit (BTO:0000486). See: PubMed
Citrus bergamia (NCBI:txid380129) Found in seed (BTO:0001226). See: PubMed
Casimiroa edulis (NCBI:txid68535) Found in seed (BTO:0001226). Methanol extract See: PubMed
Homo sapiens (NCBI:txid9606) See: MetaboLights Study
Homo sapiens (NCBI:txid9606) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-methylproline (CHEBI:90344) has role human metabolite (CHEBI:77746)
N-methylproline (CHEBI:90344) has role plant metabolite (CHEBI:76924)
N-methylproline (CHEBI:90344) is a L-proline derivative (CHEBI:84186)
N-methylproline (CHEBI:90344) is a tertiary amino compound (CHEBI:50996)
N-methylproline (CHEBI:90344) is tautomer of N-methylproline zwitterion (CHEBI:133743)
Incoming N-methylproline zwitterion (CHEBI:133743) is tautomer of N-methylproline (CHEBI:90344)
IUPAC Names
1-methyl-L-proline
1-methylproline
Synonyms Sources
(−)-N-methyl-L-proline KNApSAcK
(2S)-1-methylpyrrolidine-2-carboxylic acid PDBeChem
N-methyl-L-proline ChEBI
Manual Xrefs Databases
3BY PDBeChem
C00034881 KNApSAcK
CPD-904 MetaCyc
View more database links
Registry Numbers Types Sources
475-11-6 CAS Registry Number KNApSAcK
81103 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
10075120 PubMed citation Europe PMC
16359712 PubMed citation Europe PMC
21128667 PubMed citation Europe PMC
21838291 PubMed citation Europe PMC
25012968 PubMed citation Europe PMC
25041144 PubMed citation Europe PMC
26593620 PubMed citation Europe PMC
Last Modified
25 November 2019