CHEBI:40547 - 1-aminocyclopentanecarboxylic acid

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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 0
Average Mass 129.15700
Monoisotopic Mass 129.079
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).
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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
Manual Xrefs Databases
2798 ChemSpider
AC5 PDBeChem
C03969 KEGG COMPOUND
Cycloleucine Wikipedia
DB04620 DrugBank
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Registry Numbers Types Sources
52-52-8 CAS Registry Number NIST Chemistry WebBook
52-52-8 CAS Registry Number ChemIDplus
636626 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
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Last Modified
02 March 2016