Design, synthesis and molecular docking of new N-4-piperazinyl ciprofloxacin-triazole hybrids with potential antimicrobial activity.

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ID: 57977
2019
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Abstract
New N-4-piperazinyl ciprofloxacin-triazole hybrids 6a-o were prepared and characterized. The in vitro antimycobacterial activity revealed that compound 6a experienced promising antimycobacterial activity against Mycobactrium smegmatis compared with the reference isoniazide (INH). Additionally, compound 6a exhibited broad spectrum antibacterial activity against all the tested strains either Gram-positive or Gram-negative bacteria compared with the reference ciprofloxacin. Also, compounds 6g and 6i displayed considerable antifungal activity compared with the reference ketoconazole. DNA cleavage assay of the highly active compounds 6c and 6h showed a good correlation between the Mycobactrium cleaved DNA gyrase assay and their in vitro antimycobactrial activity. Moreover, molecular modeling studies were done for the designed ciprofloxacin derivatives to predict their binding modes towards Topoisomerase II enzyme (PDB: 5bs8).
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mohammed2019designbioorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Mohammed, Hamada H H;Abdelhafez, El-Shimaa M N;Abbas, Samar H;Moustafa, Gamal A I;Hauk, Glenn;Berger, James M;Mitarai, Satoshi;Arai, Masayoshi;Abd El-Baky, Rehab M;Abuo-Rahma, Gamal El-Din A;
Journal Bioorganic chemistry
Year 2019
DOI
S0045-2068(18)30898-8
URL
Keywords
antibacterial molecular docking Ciprofloxacin antimycobacterial antifungal dna cleavage assay

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