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153808-85-6

153808-85-6 structure
153808-85-6 structure
  • Name: Cadrofloxacin
  • Chemical Name: Cadrofloxacin
  • CAS Number: 153808-85-6
  • Molecular Formula: C19H20F3N3O4
  • Molecular Weight: 411.37500
  • Catalog: API Synthetic anti-infective drugs Quinolone
  • Create Date: 2018-08-12 13:23:29
  • Modify Date: 2024-01-05 04:28:46
  • Cadrofloxacin (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].

Name Cadrofloxacin
Synonyms 3-Quinolinecarboxylic acid,1-cyclopropyl-8-(difluoroMethoxy)-6-fluoro-1,4-dihydro-7-[(3S)-3-Methyl-1-piperazinyl]-4-oxo
1-cyclopropyl-8-(difluoromethoxy)-6-fluoro-7-[(3S)-3-methylpiperazin-1-yl]-4-oxo-quinoline-3-carboxylic acid
Caderofloxacin
Description Cadrofloxacin (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].
Related Catalog
In Vitro Cadrofloxacin against M.tuberculosis with a MIC50 of 0.25 μg/mL[1]. Cadrofloxacin against Acinetobacter spp. and Stenotrophomonas (Xanthomonas) maltophilia with MIC90s of 0.03 and 2 μg/ml, respectively[2]. Cadrofloxacin against Haemophilus influenzae, Moraxella catarrhalis, and Neisseria spp. with MIC90s less than or equal to 0.06 μg/mL[2]. Cadrofloxacin against members of the family Enterobacteriaceae with MIC90s of 0.015 to 16 μg/mL (median MIC90, 0.06 μg/mL)[2].
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]. Bryskier A, et al. Fluoroquinolones and tuberculosis. Expert Opin Investig Drugs. 2002 Feb;11(2):233-58.

[2]. Biedenbach DJ, et al. Antimicrobial activity of CS-940, a new trifluorinated quinolone. Antimicrob Agents Chemother. 1995 Oct;39(10):2325-30.

[3]. Bryskier A, et al. Fluoroquinolones and tuberculosis. Expert Opin Investig Drugs. 2002 Feb;11(2):233-58.

Density 1.458g/cm3
Boiling Point 602.4ºC at 760mmHg
Molecular Formula C19H20F3N3O4
Molecular Weight 411.37500
Flash Point 318.1ºC
Exact Mass 411.14100
PSA 83.80000
LogP 2.96700
Vapour Pressure 2.33E-15mmHg at 25°C
Index of Refraction 1.588
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