Levofloxacin | C18H20FN3O4 | CID 149096 - PubChem
Levofloxacin | C18H20FN3O4 | CID 149096 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Levofloxacin - Wikipedia
Levofloxacin is used to treat infections including: respiratory tract infections, cellulitis, urinary tract infections, prostatitis, anthrax, endocarditis, meningitis, pelvic inflammatory disease, traveler's diarrhea, tuberculosis, and plague [6][13] and is available by …
Levofloxacin: Uses, Interactions, Mechanism of Action - DrugBank …
2015年12月31日 · Levofloxacin is a fluoroquinolone antibiotic used to treat infections caused by susceptible bacteria of the upper respiratory tract, skin and skin structures, urinary tract, and prostate, as well as for post-exposure treatment of inhaled anthrax and the plague. Brand Names. Levaquin, Quinsair. Generic Name.
左氧氟沙星 - 维基百科，自由的百科全书
左氧氟沙星 （INN：levofloxacin），常见商品名 可乐必妥，是一种 广谱抗生素， [1] 用于治疗多种 细菌感染，包括急性细菌性 鼻窦炎 、 肺炎 、 幽门螺杆菌 （与其他药物联合使用）、 尿路感染 、 慢性细菌性前列腺炎 和某些类型的 肠胃炎。 [1] 与其他抗生素联用，可用于治疗 肺结核 、 脑膜炎 或 盆腔炎。 [1] 通常仅在其他选项不可用时才建议使用。 [2] 它可以通过口服、 静脉注射 [1] 和 滴眼液 形式使用。 [3] 常见的副作用包括 恶心 、 腹泻 和睡眠困难。 [1] 严重的副作用可能包括 …
Levofloxacin hydrochloride | C18H21ClFN3O4 | CID 9908810
Levofloxacin hydrochloride | C18H21ClFN3O4 | CID 9908810 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Levofloxacin - an overview | ScienceDirect Topics
Levofloxacin, the levorotatory S-enantiomer of the racemate ofloxacin, is an oral and parenteral fluoroquinolone that has bactericidal activity against a wide spectrum of Gram-negative and Gram-positive bacilli (including Streptococcus pneumoniae), as well as …
Levofloxacin - StatPearls - NCBI Bookshelf
2024年3月1日 · Levofloxacin is a broad-spectrum, third-generation fluoroquinolone antibiotic used to treat bacterial infections. Levofloxacin is a safe and effective medicine on the World Health Organization's essential medicines list. The antibiotic was patented in 1987 and subsequently received FDA approval in 1996 for medical use in the United States. [1]
Chemical structure of Levofloxacin | Download Scientific Diagram
This bacterium is highly adapted for colonization in the human stomach; the majority of these bacteria are free living in the gastric mucus layer, although about 20% are in close contact with ...
Levofloxacin - an overview | ScienceDirect Topics
The chemical structure of levofloxacin derivatives was optimized and calculated using molecular mechanics and quantum chemical methods (05MI33). A novel approach (TOMOCOMD-CARDD) to the computer-aided “rational” drug design method indicated that compound 158 (KRQ10099) was expected to be exhibited antibacterial activity (06JMM255).
Levofloxacin hemihydrate - DrugBank Online
Levofloxacin is a fluoroquinolone antibiotic and the optical S- (-) isomer of racemic ofloxacin. 1 It reportedly carries 8 to 128-fold more activity against both gram-negative and gram-positive bacteria compared to R- (+)-ofloxacin 1 and remains stereochemically stable following administration (i.e. it does not invert to the inactive isomer). 9 ...