Synthesis and antibacterial activities of optically active ofloxacin.
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DNA gyrase, topoisomerase IV, and the 4-quinolonesMechanistic study of inhibition of levofloxacin absorption by aluminum hydroxideMechanism of differential activities of ofloxacin enantiomersCrystal Structure-Based Selective Targeting of the Pyridoxal 5′-Phosphate Dependent Enzyme Kynurenine Aminotransferase II for Cognitive EnhancementIn vitro and in vivo activities of levofloxacin against Mycobacterium tuberculosisLevofloxacin versus ciprofloxacin, flucloxacillin, or vancomycin for treatment of experimental endocarditis due to methicillin-susceptible or -resistant Staphylococcus aureusIn vitro activities of levofloxacin used alone and in combination with first- and second-line antituberculous drugs against Mycobacterium tuberculosisSpectrum of activity of levofloxacin against nontuberculous mycobacteria and its activity against the Mycobacterium avium complex in combination with ethambutol, rifampin, roxithromycin, amikacin, and clofazimineScreening and its potential application of lipolytic activity from a marine environment: characterization of a novel esterase from Yarrowia lipolytica CL180.Liquid chromatographic resolution of gemifloxacin mesylate on a chiral stationary phase derived from crown ether.Characterization and its potential application of two esterases derived from the arctic sediment metagenome.Levofloxacin in vitro activity: results from an international comparative study with ofloxacin and ciprofloxacin.The evolving role of chemical synthesis in antibacterial drug discovery.Ofloxacin: its pharmacology, pharmacokinetics, and potential for clinical application.Prevalence of resistance to three fluoroquinolones: assessment of levofloxacin disk test error rates and surrogate predictors of levofloxacin susceptibility. AST Surveillance Group.In vitro and in vivo activities of QA-241, a new tricyclic quinolone derivativeAntagonism of wild-type and resistant Escherichia coli and its DNA gyrase by the tricyclic 4-quinolone analogs ofloxacin and S-25930 stereoisomers.In vitro activity of DR-3355, an optically active ofloxacinIn vitro activity of S-ofloxacin.Pharmacokinetic study of ofloxacin enantiomers in Pagrosomus major by chiral HPLC.Synergy of levofloxacin (L-ofloxacin) and oxacillin against quinolone-resistant Staphylococcus aureus, measured by the time-kill method.Novel 1-8-bridged chiral quinolones with activity against topoisomerase II: stereospecificity of the eukaryotic enzyme.Pharmacodynamics of levofloxacin, ofloxacin, and ciprofloxacin, alone and in combination with rifampin, against methicillin-susceptible and -resistant Staphylococcus aureus in an in vitro infection modelSusceptibility to levofloxacin predicted from in vitro susceptibility testing results obtained with ciprofloxacin and with ofloxacin.Investigation of enantioselective ofloxacin-albumin binding and displacement interactions using capillary affinity zone electrophoresis.Post-marketing surveillance of the safety of levofloxacin in Japan.Significance of the methyl group on the oxazine ring of ofloxacin derivatives in the inhibition of bacterial and mammalian type II topoisomerases.In vitro and in vivo antibacterial activities of E-4497, a new 3-amine-3-methyl-azetidinyl tricyclic fluoroquinolone.Nature versus nurture in two highly enantioselective esterases from Bacillus cereus and Thermoanaerobacter tengcongensis.Inhaled antibiotics for gram-negative respiratory infections.Asymmetric organocatalysis at the service of medicinal chemistrySafety and tolerability profile of second-line anti-tuberculosis medications.The stereoselectivity of drug action.Chiral separation of quinolones by liquid chromatography and capillary electrophoresis.The 4-quinolone antibiotics: past, present, and future.Organocatalytic Transfer Hydrogenation and Hydrosilylation Reactions.Quinolone-resistant mutants of escherichia coli DNA topoisomerase IV parC geneAbsorption of ofloxacin isomers in the rat small intestine.Uptake and intracellular activity of an optically active ofloxacin isomer in human neutrophils and tissue culture cells.Inhibition of DNA gyrase by optically active ofloxacin
P2860
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P2860
Synthesis and antibacterial activities of optically active ofloxacin.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年学术文章
@wuu
1986年学术文章
@zh-cn
1986年学术文章
@zh-hans
1986年学术文章
@zh-my
1986年学术文章
@zh-sg
1986年學術文章
@yue
1986年學術文章
@zh
1986年學術文章
@zh-hant
name
Synthesis and antibacterial activities of optically active ofloxacin.
@en
Synthesis and antibacterial activities of optically active ofloxacin.
@nl
type
label
Synthesis and antibacterial activities of optically active ofloxacin.
@en
Synthesis and antibacterial activities of optically active ofloxacin.
@nl
prefLabel
Synthesis and antibacterial activities of optically active ofloxacin.
@en
Synthesis and antibacterial activities of optically active ofloxacin.
@nl
P2093
P2860
P356
P1476
Synthesis and antibacterial activities of optically active ofloxacin.
@en
P2093
P2860
P304
P356
10.1128/AAC.29.1.163
P407
P577
1986-01-01T00:00:00Z