Synthesis of Fluorinated Piperazinyl Substituted Quinazolines as Potential Antibacterial Agents

Amit B. Patel, P. Patel, Kajal Patel, K. Prajapati
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引用次数: 2

Abstract

In present study, fluorinated piperazine and benzonitrile/nicotinonitrile fused quinazoline derivatives have synthesized, characterized using FT-IR, 1H & 13C NMR, 19F NMR and MS analysis and evaluated as potential antibacterial agents. They were also tested against the multidrug resistant strains. The antibacterial activity results revealed that the majority of synthesized compounds exhibited potential antibacterial with the extraordinary level of minimum inhibitory concentrations comparable to the control drugs. Moreover, the influence of presence or absence of fluoro and trifluoromethyl functional groups on the piperazine ring systems towards different biological species is elaborated. The synthesized compounds were also found non-toxic on the human cervical (HeLa) cells at their minimum inhibitory concentrations.
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本研究合成了氟化哌嗪和苯腈/烟腈熔接的喹唑啉衍生物,利用FT-IR、1H & 13C NMR、19F NMR和MS对其进行了表征,并评价其作为潜在的抗菌剂。他们还对多重耐药菌株进行了测试。抑菌活性结果表明,大多数合成的化合物具有潜在的抑菌活性,其最低抑菌浓度与对照药物相当。此外,还阐述了氟和三氟甲基官能团的存在或不存在对哌嗪环体系对不同生物物种的影响。合成的化合物在其最低抑制浓度下对人宫颈(HeLa)细胞无毒。
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