CHEBI:90344 - N-methylproline

ChEBI IDCHEBI:90344
ChEBI NameN-methylproline
Stars
ASCII NameN-methylproline
DefinitionAn L-proline derivative obtained by replacement of the amino hydrogen by a methyl group.
Last Modified25 November 2019
Submittermwilliams
DownloadsMolfile
FormulaC6H11NO2
Net Charge0
Average Mass129.159
Monoisotopic Mass129.07898
SMILESCN1CCC[C@H]1C(=O)O
InChIInChI=1S/C6H11NO2/c1-7-4-2-3-5(7)6(8)9/h5H,2-4H2,1H3,(H,8,9)/t5-/m0/s1
InChIKeyCWLQUGTUXBXTLF-YFKPBYRVSA-N
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606)
- MetaboLights (MTBLS222)
- PubMed (25041144)
Tamarix jordanis (ncbitaxon:1112732) - PubMed (16359712)
Citrus bergamia (ncbitaxon:380129)
fruit (BTO:0000486) PubMed (21128667)
seed (BTO:0001226) PubMed (21128667)
Castanea sativa (ncbitaxon:21020) kernel (BTO:0000668) PubMed (26593620)
Casimiroa edulis (ncbitaxon:68535) seed (BTO:0001226) PubMed (10075120) Methanol extract
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
N-methylproline zwitterion (CHEBI:133743) is tautomer of N-methylproline (CHEBI:90344)
IUPAC Names 
1-methylproline
1-methyl-L-proline
Synonyms  Source
N-methyl-L-prolineChEBI
(2S)-1-methylpyrrolidine-2-carboxylic acidPDBeChem
(−)-N-methyl-L-prolineKNApSAcK
Manual XrefsDatabases
3BYPDBeChem
C00034881KNApSAcK
CPD-904MetaCyc
Registry NumbersSources
Reaxys:81103Reaxys
CAS:475-11-6KNApSAcK
Citations