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Sitafloxacin Hydrate

رقم الكتالوجGC13507

هيدرات سيتافلوكساسين (DU6859a) هو مضاد حيوي فعال عن طريق الفم الفلوروكينولون مع نشاط في المختبر ضد مجموعة واسعة من البكتيريا موجبة وسالبة الجرام ، بما في ذلك البكتيريا اللاهوائية ، وكذلك ضد مسببات الأمراض غير النمطية

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Sitafloxacin Hydrate التركيب الكيميائي

Cas No.: 163253-35-8

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
128٫00
متوفر
5mg
89٫00
متوفر
10mg
164٫00
متوفر
50mg
517٫00
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com

مراجعات العميل

بناء على آراء العملاء.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

    Bioactive Compounds Premium Provider

Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Sitafloxacin Hydrate is a new-generation, broad-spectrum oral fluoroquinolone antibiotic.Target: AntibacterialSitafloxacin Hydrate, 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 [1]. In terms of clinical efficacy, oral sitafloxacin was noninferior to oral levofloxacin in the treatment of community-acquired pneumonia or an infectious exacerbation of chronic respiratory tract disease, noninferior to oral tosufloxacin in the treatment of community-acquired pneumonia, and noninferior to oral levofloxacin in the treatment of complicated urinary tract infections, according to the results of randomized, double-blind, multicentre, noninferiority trials. Noncomparative studies demonstrated the efficacy of oral sitafloxacin in otorhinolaryngological infections, urethritis in men, C. trachomatis-associated cervicitis in women and odontogenic infections [2].

References:
[1]. Anderson, D.L., Sitafloxacin hydrate for bacterial infections. Drugs Today (Barc), 2008. 44(7): p. 489-501.
[2]. Keating, G.M., Sitafloxacin: in bacterial infections. Drugs, 2011. 71(6): p. 731-44.

مراجعات

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