CHEBI:137441 - (E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one

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ChEBI Name (E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one
ChEBI ASCII Name (E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one
Definition A hydroxylamine that is N-hydroxyquinolin-4-one in which the hydrogen at position 2 has been replaced by a (1E)-non-1-en-1-yl group. It is the most active agent produced by Pseudomonas aeruginosa that modulates the growth and virulence of Staphylococcus aureus; the corresponding Z isomer is inactive.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C18H23NO2
Net Charge 0
Average Mass 285.381
Monoisotopic Mass 285.17288
InChI InChI=1S/C18H23NO2/c1-2-3-4-5-6-7-8-11-15-14-18(20)16-12-9-10-13-17(16)19(15)21/h8-14,21H,2-7H2,1H3/b11-8+
Metabolite of Species Details
Pseudomonas aeruginosa PAO1 (NCBI:txid208964) of strain PAO1 See: PubMed
Pseudomonas aeruginosa PA14 (NCBI:txid652611) of strain PA14 See: PubMed
Roles Classification
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one (CHEBI:137441) has role antibacterial agent (CHEBI:33282)
(E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one (CHEBI:137441) has role bacterial metabolite (CHEBI:76969)
(E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one (CHEBI:137441) is a hydroxylamines (CHEBI:24709)
(E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one (CHEBI:137441) is a olefinic compound (CHEBI:78840)
(E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one (CHEBI:137441) is a organic heterobicyclic compound (CHEBI:27171)
(E)-1-hydroxy-2-(non-1-en-1-yl)quinolin-4-one (CHEBI:137441) is a quinolone (CHEBI:23765)
Synonym Source
trans-N-hydroxy-Δ1-2-(non-1-enyl)-4-quinolone ChEBI
Citations Waiting for Citations Types Sources
15144975 PubMed citation Europe PMC
28523838 PubMed citation Europe PMC
Last Modified
15 June 2017