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pyrrolidin-2-one (CHEBI:36592)

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ChEBI Name pyrrolidin-2-one
ChEBI ID CHEBI:36592
Definition The simplest member of the class of pyrrolidin-2-ones, consisting of pyrrolidine in which the hydrogens at position 2 are replaced by an oxo group. The lactam arising by the formal intramolecular condensation of the amino and carboxy groups of γ-aminobutyric acid (GABA).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula Source
C4H7NO ChEBI
Net Charge 0
Average Mass 85.10450
InChI
InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)
InChIKey
HNJBEVLQSNELDL-UHFFFAOYSA-N
SMILES
O=C1CCCN1
Roles Classification
Chemical Role(s): polar solvent
A solvent that is composed of polar molecules. Polar solvents can dissolve ionic compounds or ionisable covalent compounds.
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): polar solvent
A solvent that is composed of polar molecules. Polar solvents can dissolve ionic compounds or ionisable covalent compounds.
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing pyrrolidin-2-one (CHEBI:36592) has role metabolite (CHEBI:25212)
pyrrolidin-2-one (CHEBI:36592) has role polar solvent (CHEBI:48354)
pyrrolidin-2-one (CHEBI:36592) is a pyrrolidine-2-ones (CHEBI:74223)
IUPAC Name
pyrrolidin-2-one
Synonyms Sources
1-azacyclopentan-2-one ChEBI
2-ketopyrrolidine ChemIDplus
2-oxopyrrolidine ChemIDplus
2-pyrrolidinone NIST Chemistry WebBook
2-pyrrolidone ChemIDplus
4-aminobutyric acid lactam ChemIDplus
α-pyrrolidinone NIST Chemistry WebBook
α-pyrrolidone NIST Chemistry WebBook
Butyrolactam HMDB
γ-aminobutyric acid lactam NIST Chemistry WebBook
γ-aminobutyric lactam NIST Chemistry WebBook
γ-butyrolactam NIST Chemistry WebBook
Pyrrolidinone HMDB
Pyrrolidone HMDB
Database Links Databases
2-Pyrrolidone Wikipedia
HMDB02039 HMDB
View more database links
Registry Numbers Types Sources
105241 Beilstein Registry Number Beilstein
105241 Reaxys Registry Number Reaxys
49671 Gmelin Registry Number Gmelin
616-45-5 CAS Registry Number NIST Chemistry WebBook
616-45-5 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10332870 PubMed citation CiteXplore
10403220 PubMed citation CiteXplore
10840398 PubMed citation CiteXplore
16321482 PubMed citation CiteXplore
22113027 PubMed citation CiteXplore
Last Modified
20 June 2013

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