1-aminocyclopentanecarboxylic acid (CHEBI:40547)

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ChEBI Name	1-aminocyclopentanecarboxylic acid

ChEBI ID	CHEBI:40547

Definition	A non-proteinogenic α-amino acid that is cyclopentane substituted at position 1 by amino and carboxy groups.

Stars	This entity has been manually annotated by the ChEBI Team.

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Formula

C6H11NO2

Net Charge

Average Mass

129.15700

Monoisotopic Mass

129.07898

InChI

InChI=1S/C6H11NO2/c7-6(5(8)9)3-1-2-4-6/h1-4,7H2,(H,8,9)

InChIKey

NILQLFBWTXNUOE-UHFFFAOYSA-N

SMILES

NC1(CCCC1)C(O)=O

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):	EC 2.5.1.6 (methionine adenosyltransferase) inhibitor An EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitor that interferes with the action of methionine adenosyltransferase (EC 2.5.1.6).

ChEBI Ontology
Outgoing	1-aminocyclopentanecarboxylic acid (CHEBI:40547) has role EC 2.5.1.6 (methionine adenosyltransferase) inhibitor (CHEBI:78756) 1-aminocyclopentanecarboxylic acid (CHEBI:40547) is a non-proteinogenic α-amino acid (CHEBI:83925)

IUPAC Name

1-aminocyclopentane-1-carboxylic acid

Synonyms	Sources
1-Amino-1-carboxycyclopentane	NIST Chemistry WebBook
1-Amino-1-cyclopentanecarboxylic acid	DrugBank
1-Aminocyclopentane-1-carboxylic acid	DrugBank
1-Aminocyclopentanecarboxylic acid	KEGG COMPOUND
ACPC	NIST Chemistry WebBook
Cyclo-leucine	DrugBank
Cycloleucin	ChemIDplus
Cycloleucine	KEGG COMPOUND

Last Modified

02 March 2016