Levofloxacin | C18H20FN3O4 | CID 149096 - PubChem
Levofloxacin is stereochemically stable in plasma and urine and does not invert metabolically to its enantiomer, D-ofloxacin. Levofloxacin undergoes limited metabolism in humans and is …
Levofloxacin - Wikipedia
Levofloxacin, sold under the brand name Levaquin among others, is a broad-spectrum antibiotic of the fluoroquinolone drug class. [5] .
S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl
(-)-(S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido(1,2,3-de)-1,4-benzoxazine-6-carboxylic acid, hemihydrate | C36H42F2N6O9 | CID 3033924 - structure, …
Levofloxacin hydrochloride | C18H21ClFN3O4 | CID 9908810
Levofloxacin hydrochloride | C18H21ClFN3O4 | CID 9908810 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, …
Levofloxacin | C18H20FN3O4 - ChemSpider
ChemSpider record containing structure, synonyms, properties, vendors and database links for Levofloxacin, 100986-85-4, Tavanic
LEVOFLOXACIN Structure - C18H20FN3O4 - Over 100 million chemical …
The 3D chemical structure image of LEVOFLOXACIN is based on the ball-and-stick model which displays both the three-dimensional position of the atoms and the bonds between them.
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 …
D-Levofloxacin: Uses, Interactions, Mechanism of Action
Autolysins are involved in some important biological processes such as cell separation, cell-wall turnover, competence for genetic transformation, formation of the flagella and sporulation. …
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 …
Levofloxacin is the pure (-)-(S)-enantomer of the racemic drug substance, ofloxacin. It is more soluble in water at neutral pH than ofloxacin. Chemical Name:...