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Cadrofloxacin

Cadrofloxacin Suppliers list
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Beijing HuaMeiHuLiBiological Chemical   
Tel: 010-56205725
Email: waley188@sohu.com
Company Name: SPIRO PHARMA  
Tel:
Email: eric_feng1954@126.com
Company Name: Nanjing NingFan Pharm-Tech CO. LTD.  
Tel: 17368696818
Email:
Company Name: Dideu Industries Group Limited  
Tel: +86-29-89586680 +86-15129568250
Email: 1059@dideu.com

Cadrofloxacin manufacturers

  • Cadrofloxacin
  • Cadrofloxacin pictures
  • $2500.00
  • 2026-05-11
  • CAS:153808-85-6
  • Purity:
  • Supply Ability: 10g
Cadrofloxacin Basic information
Product Name:Cadrofloxacin
Synonyms:Cadrofloxacin;Caderofloxacin;1-cyclopropyl-8-(difluoromethoxy)-6-fluoro-7-[(3S)-3-methylpiperazin-1-yl]-4-oxo-quinoline-3-carboxylic acid;3-Quinolinecarboxylic acid, 1-cyclopropyl-8-(difluoroMethoxy)-6-fluoro-1,4-dihydro-7-[(3S)-3-Methyl-1-piperazinyl]-4-oxo-;Cadrofloxacin USP/EP/BP
CAS:153808-85-6
MF:C19H20F3N3O4
MW:411.38
EINECS:
Product Categories:
Mol File:153808-85-6.mol
Cadrofloxacin Structure
Cadrofloxacin Chemical Properties
Boiling point 602.4±55.0 °C(Predicted)
density 1.458±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 10 mg/mL (24.31 mM; ultrasonic and warming and adjust pH to 3 with HCl and heat to 80°C)
pka6.40±0.50(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
Cadrofloxacin Usage And Synthesis
UsesCadrofloxacin (Caderofloxacin; CS-940), a orally active fluoroquinolone, is effective against aerobic/anaerobic Gram-positive and Gram-negative bacteria. Cadrofloxacin can be used for the research of infectious diseases[1][2][3].
in vivo

Cadrofloxacin (9 mg/kg; i.g.; once or twice daily for 14 consecutive days) increases the activity of hepatic CYP2E1 in rats[2].

Animal Model:Male Sprague-Dawley rats weighing 180-220 g[2]
Dosage:9 mg/kg
Administration:I.g. once or twice daily for 14 consecutive days
Result:Enhanced the expression of hepatic CYP2E1 mRNA, inducing a 1.6-fold increase compared with that of control rats. The level of CYP2E1 protein in the hepatic microsomes was significantly higher than control group, 190% of that in control rats.
References[1] Biedenbach DJ, et al. Antimicrobial activity of CS-940, a new trifluorinated quinolone. Antimicrob Agents Chemother. 1995 Oct;39(10):2325-30. DOI:10.1128/AAC.39.10.2325
[2] Bryskier A, et al. Fluoroquinolones and tuberculosis. Expert Opin Investig Drugs. 2002 Feb;11(2):233-58. DOI:10.1517/13543784.11.2.233
Cadrofloxacin Preparation Products And Raw materials
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