Antofloxacin hydrochloride

Antofloxacin hydrochloride Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:Antofloxacin Hydrochloride;(S)-Antofloxacin hydrochloride;Antofloxacin HCl
CAS:873888-67-6
Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel: +8613564774135
Email: zijue.cai@tsbiochem.com
Products Intro: Product Name:Antofloxacin Hydrochloride
CAS:873888-67-6
Package:50mg;2180USD|25mg;1670USD|100mg;2800USD
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Products Intro: Product Name:Antofloxacin hydrochloride
CAS:873888-67-6
Purity:>=95% Remarks:Reach out to us for more information about custom solutions.
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:Antofloxacin Hydrochloride
CAS:873888-67-6
Package:50mg/RMB 15300;25mg/RMB 11700;100mg/RMB 19500

Antofloxacin hydrochloride manufacturers

Antofloxacin hydrochloride Basic information
Product Name:Antofloxacin hydrochloride
Synonyms:Antofloxacin hydrochloride;(S)-Antofloxacin hydrochloride;Antofloxacin HCl
CAS:873888-67-6
MF:C18H22ClFN4O4
MW:412.85
EINECS:
Product Categories:
Mol File:873888-67-6.mol
Antofloxacin hydrochloride Structure
Antofloxacin hydrochloride Chemical Properties
Safety Information
MSDS Information
Antofloxacin hydrochloride Usage And Synthesis
UsesAntofloxacin hydrochloride is a well tolerate, orally active and broad-spectrum 8-amino-fluoroquinolone with potent antibacterial activities. Antofloxacin hydrochloride shows superior antibacterial activity against gyrA mutation-positive H. pylori strains, especially in Asn87- mutated strains, compared to levofloxacin. Antofloxacin hydrochloride is a weak, reversible inhibitor of CYP1A2 for the research of infections caused by a diverse group of bacterial species[1][2][3].
in vivo

Antofloxacin (2.5~160 mg/kg; s.c.; 24 hours) penetration ratio ranges from 1.22 to 1.54 for the total drug concentrations and is independent of the dose levels[3]. Antofloxacin increases the plasma theophylline concentration, partly by acting as a mechanism based inhibitor of CYP1A2. Antofloxacin inhibits the formation of the three metabolites of theophylline was time-, concentration- and NADPH-dependent, which is characteristic of mechanism-based inhibition[2].

Animal Model:Mice (Pharmacokinetic Analysis)[3]
Dosage:2.5~160 mg/kg
Administration:S.c.; 24 hours
Result:Penetration ratio ranged from 1.22 to 1.54 for the total drug concentrations and was independent of the dose levels.
IC 50Quinolone
References[1] He XJ, et al. Efficacy and Safety of Antofloxacin-Based Triple Therapy for Helicobacter pylori Eradication Failure in China [published online ahead of print, 2021 Feb 8]. Dig Dis Sci. 2021;10.1007/s10620-021-06856-z. DOI:10.1007/s10620-021-06856-z
[2] Liu L, et al. Modulation of pharmacokinetics of theophylline by antofloxacin, a novel 8-amino-fluoroquinolone, in humans. Acta Pharmacol Sin. 2011;32(10):1285-1293. DOI:10.1038/aps.2011.78
[3] Zhou YF, et al. In Vivo Pharmacokinetic and Pharmacodynamic Profiles of Antofloxacin against Klebsiella pneumoniae in a Neutropenic Murine Lung Infection Model. Antimicrob Agents Chemother. 2017;61(5):e02691-16. Published 2017 Apr 24. DOI:10.1128/AAC.02691-16
Antofloxacin hydrochloride Preparation Products And Raw materials
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