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For: Fedorowicz J, Sączewski J. Modifications of quinolones and fluoroquinolones: hybrid compounds and dual-action molecules. Monatsh Chem 2018;149:1199-245. [PMID: 29983452 DOI: 10.1007/s00706-018-2215-x] [Cited by in Crossref: 47] [Cited by in F6Publishing: 49] [Article Influence: 9.4] [Reference Citation Analysis]
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15 Varkhedkar R, Yang F, Dontha R, Zhang J, Liu J, Spingler B, van der Veen S, Duttwyler S. Natural-Product-Directed Catalytic Stereoselective Synthesis of Functionalized Fused Borane Cluster-Oxazoles for the Discovery of Bactericidal Agents. ACS Cent Sci 2022;8:322-31. [PMID: 35350606 DOI: 10.1021/acscentsci.1c01132] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
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17 Luo X. Mechanism of levofloxacin, tobramycin, and azithromycin in the treatment of bacterial conjunctivitis. 7TH INTERNATIONAL CONFERENCE ON MATHEMATICS: PURE, APPLIED AND COMPUTATION: Mathematics of Quantum Computing 2022. [DOI: 10.1063/5.0113013] [Reference Citation Analysis]
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19 López Y, Muñoz L, Gargallo-Viola D, Cantón R, Vila J, Zsolt I. Uptake of Ozenoxacin and Other Quinolones in Gram-Positive Bacteria. Int J Mol Sci 2021;22:13363. [PMID: 34948159 DOI: 10.3390/ijms222413363] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
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22 Aura Rusu, Ioana-Andreea Lungu, Octavia-Laura Moldovan, Corneliu Tanase, Gabriel Hancu. Structural Characterization of the Millennial Antibacterial (Fluoro)Quinolones—Shaping the Fifth Generation. Pharmaceutics 2021;13:1289. [PMID: 34452252 DOI: 10.3390/pharmaceutics13081289] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 8.0] [Reference Citation Analysis]
23 Desiatkina O, Johns SK, Anghel N, Boubaker G, Hemphill A, Furrer J, Păunescu E. Synthesis and Antiparasitic Activity of New Conjugates—Organic Drugs Tethered to Trithiolato-Bridged Dinuclear Ruthenium(II)–Arene Complexes. Inorganics 2021;9:59. [DOI: 10.3390/inorganics9080059] [Reference Citation Analysis]
24 Alaaeldin R, Mustafa M, Abuo-Rahma GEA, Fathy M. In vitro inhibition and molecular docking of a new ciprofloxacin-chalcone against SARS-CoV-2 main protease. Fundam Clin Pharmacol 2021. [PMID: 34268806 DOI: 10.1111/fcp.12708] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
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29 Surur AS, Sun D. Macrocycle-Antibiotic Hybrids: A Path to Clinical Candidates. Front Chem 2021;9:659845. [PMID: 33996753 DOI: 10.3389/fchem.2021.659845] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
30 Gultekin E, Bekircan O, Kolcuoğlu Y, Akdemir A. Synthesis of new 1,2,4-triazole-(thio)semicarbazide hybrid molecules: Their tyrosinase inhibitor activities and molecular docking analysis. Arch Pharm (Weinheim) 2021;354:e2100058. [PMID: 33900640 DOI: 10.1002/ardp.202100058] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
31 Al-Wahaibi LH, Amer AA, Marzouk AA, Gomaa HAM, Youssif BGM, Abdelhamid AA. Design, Synthesis, and Antibacterial Screening of Some Novel Heteroaryl-Based Ciprofloxacin Derivatives as DNA Gyrase and Topoisomerase IV Inhibitors. Pharmaceuticals (Basel) 2021;14:399. [PMID: 33922361 DOI: 10.3390/ph14050399] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 4.5] [Reference Citation Analysis]
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33 Verma K, Mahalapbutr P, Suriya U, Somboon T, Aiebchun T, Shi L, Maitarad P, Rungrotmongkol T. In Silico Screening of DNA Gyrase B Potent Flavonoids for the Treatment of Clostridium difficile Infection from PhytoHub Database. Braz arch biol technol 2021;64:e21200402. [DOI: 10.1590/1678-4324-2021200402] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
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35 Periyan D, Chinnasamy U. Maleimide-g-pyridine Octadecene Polymers: Synthesis, Characterization, Thermal Stability, Fluorescence and Biological Studies. Asian J Chem 2021;33:459-464. [DOI: 10.14233/ajchem.2021.22549] [Reference Citation Analysis]
36 Bokhtia RM, Panda SS, Girgis AS, Honkanadavar HH, Ibrahim TS, George RF, Kashef MT, Fayad W, Sakhuja R, Abdel-aal EH, Al-mahmoudy AMM. Fluoroquinolone-3-carboxamide Amino Acid Conjugates: Synthesis, Antibacterial Properties And Molecular Modeling Studies. MC 2020;17:71-84. [DOI: 10.2174/1573406415666190904143852] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
37 Dalhoff A. Selective toxicity of antibacterial agents-still a valid concept or do we miss chances and ignore risks? Infection 2021;49:29-56. [PMID: 33367978 DOI: 10.1007/s15010-020-01536-y] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
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39 Marciniec K, Beberok A, Pęcak P, Boryczka S, Wrześniok D. Ciprofloxacin and moxifloxacin could interact with SARS-CoV-2 protease: preliminary in silico analysis. Pharmacol Rep 2020;72:1553-61. [PMID: 33063271 DOI: 10.1007/s43440-020-00169-0] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 6.3] [Reference Citation Analysis]
40 Kraft O, Kozubek M, Hoenke S, Serbian I, Major D, Csuk R. Cytotoxic triterpenoid-safirinium conjugates target the endoplasmic reticulum. Eur J Med Chem 2021;209:112920. [PMID: 33049606 DOI: 10.1016/j.ejmech.2020.112920] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
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42 Kasabri V, Arabiyat S, Al-hiari Y, Zalloum H, Almaliti J, Telfah A, Bustanji YK, Alalawi S. Fluoroquinolones as a potentially novel class of antidiabesity and antiproliferative compounds: synthesis and docking studies. Can J Chem 2020;98:635-45. [DOI: 10.1139/cjc-2020-0162] [Reference Citation Analysis]
43 Ciura K, Fedorowicz J, Kapica H, Adamkowska A, Sawicki W, Sączewski J. Affinity of Fluoroquinolone–Safirinium Dye Hybrids to Phospholipids Estimated by IAM-HPLC. Processes 2020;8:1148. [DOI: 10.3390/pr8091148] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
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