CHEBI:17289 - homoserine lactone

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ChEBI Name homoserine lactone ChEBI ID CHEBI:17289 Definition A butan-4-olide having an amino substituent at the 2-position. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:11522, CHEBI:1017, CHEBI:19468, CHEBI:30656 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C4H7NO2 Net Charge 0 Average Mass 101.10392 Monoisotopic Mass 101.04768 InChI InChI=1S/C4H7NO2/c5-3-1-2-7-4(3)6/h3H,1-2,5H2 InChIKey QJPWUUJVYOJNMH-UHFFFAOYSA-N SMILES NC1CCOC1=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 ) Biological Role(s): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. View more via ChEBI Ontology ChEBI Ontology Outgoing homoserine lactone (CHEBI:17289) has role Escherichia coli metabolite (CHEBI:76971) homoserine lactone (CHEBI:17289) is a butan-4-olide (CHEBI:22950) homoserine lactone (CHEBI:17289) is a primary amino compound (CHEBI:50994) homoserine lactone (CHEBI:17289) is conjugate base of homoserinium lactone (CHEBI:58093) Incoming N-acyl homoserine lactone (CHEBI:83169) has functional parent homoserine lactone (CHEBI:17289) D-homoserine lactone (CHEBI:30657) is a homoserine lactone (CHEBI:17289) L-homoserine lactone (CHEBI:30655) is a homoserine lactone (CHEBI:17289) homoserinium lactone (CHEBI:58093) is conjugate acid of homoserine lactone (CHEBI:17289) IUPAC Names 3-amino-4,5-dihydrofuran-2(3H)-one homoserine lactone Synonyms Sources 2-Aminobutan-4-olide KEGG COMPOUND α-amino-γ-butyrolactone ChEBI Homoserine lactone KEGG COMPOUND Hsl IUPAC HSL ChEBI HSLs ChEBI Manual Xrefs Databases C02926 KEGG COMPOUND DB02624 DrugBank HOMOSERINE-LACTONE MetaCyc View more database links Registry Numbers Types Sources 1192-20-7 CAS Registry Number ChemIDplus 80584 Beilstein Registry Number Beilstein 80584 Reaxys Registry Number Reaxys Citation Type Source 7545940 PubMed citation Europe PMC Last Modified 29 September 2014