(-)-Ofloxacin hydrochloride MedChemExpress (MCE)

Product Name	Levofloxacin Hydrochloride
Synonyms	LEVOFLOXACIN HCL LevofloxacinHydrochloride LEVOFLOXACIN HYDROCHLORIDE Levofloxacin Hydrochloride carboxylic acid monohydrochloride -9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl) -7-oxo-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid hydrochloride Synonyms LEVOFLOXACIN HCL LevofloxacinHydrochloride LEVOFLOXACIN HYDROCHLORIDE Levofloxacin Hydrochloride carboxylic acid monohydrochloride -9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl) -7-oxo-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid hydrochloride (S)-9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid hydrochloride (3S)-9-fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid hydrochloride 3S)-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 Monohydrochlori (3S)-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 monohydrochloride
CAS	177325-13-2
EINECS	605-797-4
Chemical Formula	C18H21ClFN3O4
Molecular Weight	397.83
inchi	InChI=1/C18H20FN3O4.ClH/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21;/h7-8,10H,3-6,9H2,1-2H3,(H,24,25);1H/t10-;/m0./s1
Package	1 g
Price	Email to quote
Descriptions	Levofloxacin hydrochloride Levofloxacin hydrochloride MedChemExpress (MCE) HY-B0330B 177325-13-2 (-)-Ofloxacin hydrochloride 98.0% 4°C, sealed storage, away from moisture In solvent : -80°C, 6 months Descriptions Levofloxacin hydrochloride Levofloxacin hydrochloride MedChemExpress (MCE) HY-B0330B 177325-13-2 (-)-Ofloxacin hydrochloride 98.0% 4°C, sealed storage, away from moisture In solvent : -80°C, 6 months -20°C, 1 month (sealed storage, away from moisture) Room temperature in continental US may vary elsewhere. Levofloxacin ((-)-Ofloxacin) hydrochloride is an orally active antibiotic and is active against both Gram-positive and Gram-negative bacteria. Levofloxacin hydrochloride inhibits the DNA gyrase and topoisomerase IV. Levofloxacin hydrochloride can be used for chronic periodontitis, airway inflammation and BK Viremia research. Levofloxacin hydrochloride shows anti-orthopoxvirus activity. TOPO IV \| \| \| \| \| \| \| \| \| \| [1]. Siva, R., et al., Effect of levofloxacin on neutrophilic airway inflammation in stable COPD: a randomized, double-blind, placebo-controlled trial. Int J Chron Obstruct Pulmon Dis, 2014. 9: p. 179-86. [Content Brief] [2]. Pradeep, A.R., et al., Clinical and microbiological effects of levofloxacin in the treatment of chronic periodontitis: a randomized, placebo-controlled clinical trial. J Investig Clin Dent, 2014. [Content Brief] [3]. Lee, B.T., et al., Efficacy of Levofloxacin in the Treatment of BK Viremia: A Multicenter, Double-Blinded, Randomized, Placebo-Controlled Trial. Clin J Am Soc Nephrol, 2014. [Content Brief] [4]. Drlica K, et al. DNA gyrase, topoisomerase IV, and the 4-quinolones. Microbiol Mol Biol Rev. 1997 Sep 61(3):377-92. [Content Brief] [5]. Smee DF, et al. A review of compounds exhibiting anti-orthopoxvirus activity in animal models. Antiviral Res. 2003 Jan 57(1-2):41-52. [Content Brief]
Last Update	2025-04-01 14:45:47

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