Hot Selling High Quality Sitafloxacin Hydrate Cas 163253-35-8 With Reasonable Price And Fast Delivery

Sitafloxacin hydrate CAS 163253-35-8 has a molecular formula of 2(C19H18ClF2N3O3).3(H2O) and a molecular weight of 873.67. It is a derivative of Sitafloxacin. Sitafloxacin hydrate CAS 163253-35-8 is a new-generation, broad-spectrum oral fluoroquinolone that is very active against many Gram-positive, Gram-negative and anaerobic clinical isolates, including strains resistant to other fluoroquinolones, was recently approved in Japan for the treatment of respiratory and urinary tract infections. Sitafloxacin is active against methicillin-resistant staphylococci, Streptococcus pneumoniae and other streptococci with reduced susceptibility to levofloxacin and other quinolones and enterococci. Sitafloxacin has also demonstrated activity against clinical isolates of Klebsiella pneumoniae (including about 67% of strains producing extended-spectrum, beta-lactamases and resistant to ciprofloxacin), Enterobacter cloacae, Pseudomonas aeruginosa with some activity against quinolone-resistant strains and Acinetobacter baumannii. The in vitro activity against anaerobes is comparable to imipenem or metronidazole.
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Product Details

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Product Description

Name

Hot selling high quality Sitafloxacin hydrate cas 163253-35-8 with reasonable price and fast delivery

Other name

Gracevit ;

Sitafloxacin;

DU-6859a ;

Sitafloxacin monohydrate

CAS

163253-35-8

Applications

API

Appearance

White to light yellow crystalline powder

Sitafloxacin hydrate CAS 163253-35-8 has a molecular formula of 2(C19H18ClF2N3O3).3(H2O) and a molecular weight of 873.67. It is a derivative of Sitafloxacin.

Sitafloxacin hydrate CAS 163253-35-8 is a new-generation, broad-spectrum oral fluoroquinolone that is very active against many Gram-positive, Gram-negative and anaerobic clinical isolates, including strains resistant to other fluoroquinolones, was recently approved in Japan for the treatment of respiratory and urinary tract infections. Sitafloxacin is active against methicillin-resistant staphylococci, Streptococcus pneumoniae and other streptococci with reduced susceptibility to levofloxacin and other quinolones and enterococci. Sitafloxacin has also demonstrated activity against clinical isolates of Klebsiella pneumoniae (including about 67% of strains producing extended-spectrum, beta-lactamases and resistant to ciprofloxacin), Enterobacter cloacae, Pseudomonas aeruginosa with some activity against quinolone-resistant strains and Acinetobacter baumannii. The in vitro activity against anaerobes is comparable to imipenem or metronidazole.

 

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