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47 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
8393112 12 Quinolone antibacterials: synthesis and biological activity of carbon isosteres of the 1-piperazinyl and 3-amino-1-pyrrolidinyl side chains.EBI Warner-Lambert
3346869 16 7-substituted 5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3- quinolinecarboxylic acids: synthesis and biological activity of a new class of quinolone antibacterials.EBI Warner-Lambert
15125947 38 Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity.EBI Dainippon Pharmaceutical
11378377 11 Fine Tuning of physico-chemical parameters to optimise a new series of novobiocin analogues.EBI Aventis Pharma
9871636 17 DNA gyrase inhibitory activity of ellagic acid derivatives.EBI R. W. Johnson Pharmaceutical Research Institute
26363871 7 Discovery of WQ-3810: Design, synthesis, and evaluation of 7-(3-alkylaminoazetidin-1-yl)fluoro-quinolones as orally active antibacterial agents.EBI Wakunaga Pharmaceutical
25286019 18 Novel DNA gyrase inhibiting spiropyrimidinetriones with a benzisoxazole scaffold: SAR and in vivo characterization.EBI Astrazeneca
26098163 66 Discovery of 4,5,6,7-Tetrahydrobenzo[1,2-d]thiazoles as Novel DNA Gyrase Inhibitors Targeting the ATP-Binding Site.EBI University of Ljubljana
25951434 4 Search for factors affecting antibacterial activity and toxicity of 1,2,4-triazole-ciprofloxacin hybrids.EBI Medical University
25238443 11 Synthesis, structure-activity relationship studies, and antibacterial evaluation of 4-chromanones and chalcones, as well as olympicin A and derivatives.EBI University of Hawaii At Hilo
15715489 4 Chiral DNA gyrase inhibitors. 3. Probing the chiral preference of the active site of DNA gyrase. Synthesis of 10-fluoro-6-methyl-6,7-dihydro-9-piperazinyl- 2H-benzo[a]quinolizin-20-one-3-carboxylic acid analogues.EBI University of Kansas
18268084 2 DNA gyrase from the albicidin producer Xanthomonas albilineans has multiple-antibiotic-resistance and unusual enzymatic properties.EBI The University of Queensland
17064062 4 3-aminoquinazolinediones as a new class of antibacterial agents demonstrating excellent antibacterial activity against wild-type and multidrug resistant organisms.EBI Pfizer
16392790 12 Isothiazolopyridones: synthesis, structure, and biological activity of a new class of antibacterial agents.EBI Achillion Pharmaceuticals
16337791 34 Isothiazoloquinolones containing functionalized aromatic hydrocarbons at the 7-position: synthesis and in vitro activity of a series of potent antibacterial agents with diminished cytotoxicity in human cells.EBI Achillion Pharmaceuticals
14623007 5 Structure-activity relationship in the oxazolidinone-quinolone hybrid series: influence of the central spacer on the antibacterial activity and the mode of action.EBI Morphochem
32234278 11 Identification of an ethyl 5,6-dihydropyrazolo[1,5-c]quinazoline-1-carboxylate as a catalytic inhibitor of DNA gyrase.EBI University of Iowa
32634310 8 Topoisomerase Inhibitors Addressing Fluoroquinolone Resistance in Gram-Negative Bacteria.EBI Novartis Institutes For Biomedical Research
32027491 4 Two Decades of Successful SAR-Grounded Stories of the Novel Bacterial Topoisomerase Inhibitors (NBTIs).EBI National Institute of Chemistry
30846404 34 Discovery and development of novel rhodanine derivatives targeting enoyl-acyl carrier protein reductase.EBI Nanjing University
31279292 3 Synthesis and biological evaluation of hybrid quinolone-based quaternary ammonium antibacterial agents.EBI Medical University of Gdansk
31276392 176 Virtual Screening Approach and Investigation of Structure-Activity Relationships To Discover Novel Bacterial Topoisomerase Inhibitors Targeting Gram-Positive and Gram-Negative Pathogens.EBI Angelini
31015103 2 1,2,4-Triazole-quinoline/quinolone hybrids as potential anti-bacterial agents.EBI Henan University of Chinese Medicine
30962087 21 Structure-guided design of antibacterials that allosterically inhibit DNA gyrase.EBI Glaxosmithkline
25317480 4 Second-generation antibacterial benzimidazole ureas: discovery of a preclinical candidate with reduced metabolic liability.EBI Vertex Pharmaceuticals
24882676 6 Novel 3-arylfuran-2(5H)-one-fluoroquinolone hybrid: design, synthesis and evaluation as antibacterial agent.EBI Jishou University
20404126 20 Comparison of in vitro activities of fluoroquinolone-like 2,4- and 1,3-diones.EBI University of Minnesota Medical School
16087337 6 Synthesis and antibacterial activity of a novel series of DNA gyrase inhibitors: 5-[(E)-2-arylvinyl]pyrazoles.EBI Dainippon Pharmaceutical
15214796 5 Synthesis and antibacterial activity of a novel series of potent DNA gyrase inhibitors. Pyrazole derivatives.EBI Dainippon Pharmaceutical
12904069 24 Discovery of (3S)-amino-(4R)-ethylpiperidinyl quinolones as potent antibacterial agents with a broad spectrum of activity and activity against resistant pathogens.EBI Procter & Gamble Pharmaceuticals
8960555 13 Potent 6-desfluoro-8-methylquinolones as new lead compounds in antibacterial chemotherapy.EBI Universit£
8385225 16 Quinolone antibacterials containing the new 7-[3-(1-aminoethyl)-1- pyrrolidinyl] side chain: the effects of the 1-aminoethyl moiety and its stereochemical configurations on potency and in vivo efficacy.EBI Warner-Lambert
29727185 2 Discovery and Optimization of Indolyl-Containing 4-Hydroxy-2-Pyridone Type II DNA Topoisomerase Inhibitors Active against Multidrug Resistant Gram-negative Bacteria.EBI Ptc Therapeutics
29596745 13 Imidazopyrazinones (IPYs): Non-Quinolone Bacterial Topoisomerase Inhibitors Showing Partial Cross-Resistance with Quinolones.EBI Sanofi R&D
29661533 7 Design, synthesis, and evaluation of novel N-1 fluoroquinolone derivatives: Probing for binding contact with the active site tyrosine of gyrase.EBI University of Iowa
18690678 66 Novel dual-targeting benzimidazole urea inhibitors of DNA gyrase and topoisomerase IV possessing potent antibacterial activity: intelligent design and evolution through the judicious use of structure-guided design and structure-activity relationships.BDB Vertex Pharmaceuticals