Aguilera R, Gutierrez OL, Sumano LH: Enhancement of enrofloxacin serum antibacterial activity by calcium primed broilers.
Salmon SA, Watts JL, Case CA, Hoffman LJ, Wegener HC, Yancey RJ Jr: Comparison of MICs of ceftiofur and other antimicrobial agents against bacterial pathogens of swine from the United States, Canada, and Denmark.Schroder J: Enrofloxacin: a new antimicrobial agent.Dimitrova DJ, Lashev LD, Yanev SG, Pandova B: Pharmacokinetics of enrofloxacin in turkeys.Kan CA: Pharmacokinetics of enrofloxacin in chicken.e Souza MJ, Bittencourt CF, e Souza Filho Pda S: Microbiological assay for enrofloxacin injection.e Souza MJ, Bittencourt CF, Morsch LM: LC determination of enrofloxacin.Bowser PR, Babish JG: Enrofloxacin in salmonids.Lizondo M, Pons M, Gallardo M, Estelrich J: Physicochemical properties of enrofloxacin.Kingdom Organic compounds Super Class Organoheterocyclic compounds Class Quinolines and derivatives Sub Class Quinoline carboxylic acids Direct Parent Quinoline carboxylic acids Alternative Parents N-arylpiperazines / Fluoroquinolones / Aminoquinolines and derivatives / Hydroquinolones / Haloquinolines / Hydroquinolines / Pyridinecarboxylic acids / Dialkylarylamines / N-alkylpiperazines / Aryl fluorides / Benzenoids / Vinylogous amides / Heteroaromatic compounds / Trialkylamines / Amino acids / Azacyclic compounds / Carboxylic acids / Monocarboxylic acids and derivatives / Organic oxides / Organopnictogen compounds / Organooxygen compounds / Organofluorides / Hydrocarbon derivativesĬCN1CCN(CC1)C1=CC2=C(C=C1F)C(=O)C(=CN2C1CC1)C(O)=O References General References These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions. Cytochrome P-450 CYP1A2 Inhibitors (strength unknown)Ĭhemical Taxonomy Provided by Classyfire Description This compound belongs to the class of organic compounds known as quinoline carboxylic acids.