CHEBI:6198 - (S)-azetidine-2-carboxylic acid

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ChEBI Name (S)-azetidine-2-carboxylic acid
ChEBI ASCII Name (S)-azetidine-2-carboxylic acid
Definition The (S)-enantiomer of azetidine-2-carboxylic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C4H7NO2
Net Charge 0
Average Mass 101.10392
Monoisotopic Mass 101.048
InChI InChI=1S/C4H7NO2/c6-4(7)3-1-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m0/s1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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.
(via azetidine-2-carboxylic acid )
teratogenic agent
A role played by a chemical compound in biological systems with adverse consequences in embryo developments, leading to birth defects, embryo death or altered development, growth retardation and functional defect.
(via azetidine-2-carboxylic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (S)-azetidine-2-carboxylic acid (CHEBI:6198) is a azetidine-2-carboxylic acid (CHEBI:38108)
(S)-azetidine-2-carboxylic acid (CHEBI:6198) is enantiomer of (R)-azetidine-2-carboxylic acid (CHEBI:38109)
Incoming (S,R,R)-nicotianamine (CHEBI:38115) has functional parent (S)-azetidine-2-carboxylic acid (CHEBI:6198)
(S,S,S)-nicotianamine (CHEBI:17721) has functional parent (S)-azetidine-2-carboxylic acid (CHEBI:6198)
(R)-azetidine-2-carboxylic acid (CHEBI:38109) is enantiomer of (S)-azetidine-2-carboxylic acid (CHEBI:6198)
(2S)-azetidine-2-carboxylic acid
Synonyms Sources
(S)-(-)-Azetidine-2-carboxylic acid KEGG COMPOUND
(S)-2-azetidinecarboxylic acid ChemIDplus
(S)-azetidine-2-carboxylic acid ChemIDplus
Azetidyl-2-carboxylic acid KEGG COMPOUND
L-Azetidine 2-carboxylic acid KEGG COMPOUND
Manual Xrefs Databases
C00001343 KNApSAcK
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Registry Numbers Types Sources
2133-34-8 CAS Registry Number ChemIDplus
3648544 Beilstein Registry Number Beilstein
80678 Beilstein Registry Number Beilstein
80678 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1101962 PubMed citation Europe PMC
5041194 PubMed citation Europe PMC
Last Modified
28 July 2014