Design, synthesis, molecular docking, and antibacterial activity evaluation of some novel norfloxacin analogues
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ONIGA, Smaranda Dafina, PALAGE, Mariana Doina, ARANICIU, Cătălin, MARC, Gabriel, ONIGA, Ovidiu, VLASE, Laurian, PRISAKARI, Viorel I., VALICA, Vladimir, CURLAT, Serghei, UNCU, Livia. Design, synthesis, molecular docking, and antibacterial activity evaluation of some novel norfloxacin analogues. In: Farmacia, 2018, nr. 6(66), pp. 1048-1058. ISSN 0014-8237. DOI: https://doi.org/10.31925/FARMACIA.2018.6.19
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Farmacia
Numărul 6(66) / 2018 / ISSN 0014-8237

Design, synthesis, molecular docking, and antibacterial activity evaluation of some novel norfloxacin analogues

DOI:https://doi.org/10.31925/FARMACIA.2018.6.19

Pag. 1048-1058

Oniga Smaranda Dafina1, Palage Mariana Doina1, Araniciu Cătălin1, Marc Gabriel1, Oniga Ovidiu1, Vlase Laurian1, Prisakari Viorel I.2, Valica Vladimir2, Curlat Serghei2, Uncu Livia2
 
1 Iuliu Haţieganu University of Medicine and Pharmacy Cluj-Napoca,
2 ”Nicolae Testemițanu” State University of Medicine and Pharmacy
 
 
Disponibil în IBN: 16 aprilie 2019


Rezumat

A novel series of 7 or 3-substituted norfloxacin derivatives were synthesized and characterized by1H NMR, MS and elemental analysis techniques. All the synthesized compounds were evaluated for antimicrobial activity against both Gram-positive and Gram-negative bacteria and the MIC and MBC values were calculated by the broth dilution method. To understand the influence of the different type of substituents on the pharmacokinetic properties and the interaction with the target enzyme of fluoroquinolones (DNA gyrase), we performed a molecular docking study, and we calculated the ADMET properties.

Cuvinte-cheie
DNA gyrase, Molecular docking, Norfloxacin