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CHEBI:40547 - 1-aminocyclopentanecarboxylic acid

ChEBI IDCHEBI:40547
ChEBI Name1-aminocyclopentanecarboxylic acid
Stars
DefinitionA non-proteinogenic α-amino acid that is cyclopentane substituted at position 1 by amino and carboxy groups.
Last Modified2 March 2016
DownloadsMolfile
FormulaC6H11NO2
Net Charge0
Average Mass129.159
Monoisotopic Mass129.07898
SMILESNC1(C(=O)O)CCCC1
InChIInChI=1S/C6H11NO2/c7-6(5(8)9)3-1-2-4-6/h1-4,7H2,(H,8,9)
InChIKeyNILQLFBWTXNUOE-UHFFFAOYSA-N
Wikipedia
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
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 Relation(s)
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  Source
CycloleucineKEGG COMPOUND
Cyclo-leucineDrugBank
1-Aminocyclopentane-1-carboxylic acidDrugBank
1-Amino-1-cyclopentanecarboxylic acidDrugBank
CycloleucinChemIDplus
1-Amino-1-carboxycyclopentaneNIST Chemistry WebBook
Manual XrefsDatabases
AC5PDBeChem
C03969KEGG COMPOUND
DB04620DrugBank
CycloleucineWikipedia
2798ChemSpider
Registry NumbersSources
Reaxys:636626Reaxys
CAS:52-52-8KEGG COMPOUND
CAS:52-52-8ChemIDplus
CAS:52-52-8NIST Chemistry WebBook
Citations