2-tridecyl-4-quinolone (PAMDB120678)

IdentificationTaxonomyPhysical PropertiesBiological PropertiesSpectraConcentrationsLinksReferencesEnzymes Transporters
Proteins (3280)
Record Information
Version 1.0
Update Date 1/22/2018 11:54:54 AM
Metabolite IDPAMDB120678
Identification
Name: 2-tridecyl-4-quinolone
Description:Pseudomonas aeruginosa alkyl-quinolones (AQs) are small molecule metabolites produced by Pseudomonas aeruginosa . Pseudomonas aeruginosa produces over 55 AQ species, many of which have unknown biological functions. AQ production in Pseudomonas aeruginosa is dependent on the activity of the gene pqsA, which converts anthranilate to anthraniloyl-CoA. Production of the resulting AQs is mediated by the activity of enzymes encoded by the pqs operon.
Structure
Thumb
🔍MOLSDFPDBSMILESInChIView Structure
Synonyms:2-tridecylquinolin-4-ol
Chemical Formula: C22H33NO
Average Molecular Weight: 327.5035
Monoisotopic Molecular Weight: 327.2562
InChI Key: FNWGQRPIGZVQLF-UHFFFAOYSA-N
InChI:InChI=1S/C22H33NO/c1-2-3-4-5-6-7-8-9-10-11-12-15-19-18-22(24)20-16-13-14-17-21(20)23-19/h13-14,16-18H,2-12,15H2,1H3,(H,23,24)
CAS number: Not Available
IUPAC Name:Not Available
Traditional IUPAC Name: Not Available
SMILES:OC1=CC(CCCCCCCCCCCCC)=NC2=C1C=CC=C2
Chemical Taxonomy
Taxonomy DescriptionThis compound belongs to the class of organic compounds known as hydroxyquinolones. These are compounds containing a quinoline moiety bearing a hydroxyl group and a ketone. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.
Kingdom Organic compounds
Super ClassOrganoheterocyclic compounds
Class Quinolines and derivatives
Sub ClassQuinolones and derivatives
Direct Parent Hydroxyquinolones
Alternative Parents
Substituents
  • Hydroxyquinolone
  • Dihydroquinolone
  • Hydroxyquinoline
  • Dihydroquinoline
  • Hydroxypyridine
  • Benzenoid
  • Pyridine
  • Heteroaromatic compound
  • Vinylogous amide
  • Azacycle
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Aromatic heteropolycyclic compound
Molecular Framework Aromatic heteropolycyclic compounds
External Descriptors
  • quinolone (CHEBI:29472)
  • a tautomer (CPD-12838)
Physical Properties
State: Not Available
Charge:Not Available
Melting point: Not Available
Experimental Properties: Not Available
Predicted Properties
PropertyValueSource
Boiling Point 887.92 [K]ChemDraw
Melting Point 592.1 [K}ChemDraw
Critical Temp 897.05 [K]ChemDraw
Critical Pres 14.58 [Bar]ChemDraw
Critical Vol 1146.5 [cm3/mol]ChemDraw
Gibbs Energy 266.22 [kJ/mol]ChemDraw
Log P 7.51ChemDraw
MR 101.91 [cm3/mol]ChemDraw
Heat of Form -225.8 [kJ/mol]ChemDraw
tPSA 32.59ChemDraw
CLogP 8.209ChemDraw
CMR 10.348ChemDraw
Biological Properties
Cellular Locations: Not Available
Reactions:Not Available
Pathways: Not Available
Spectra
Spectra: Not Available
References
References:
  • Lepine F, Milot S, Deziel E, He J, Rahme LG. Electrospray/Mass Spectrometric Identification and Analysis of 4-Hydroxy-2-Alkylquinolines (HAQs) Produced by Pseudomonas aeruginosa . Appl Microbiol Biotechnol. 2010; 86(5):1323-36. Pubmed: 15144975
Synthesis Reference: Not Available
Material Safety Data Sheet (MSDS) Not Available
External Links: Not Available