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首页> 外文期刊>Oriental Journal of Chemistry: An International Research Journal of Pure & Applied Chemistry >Synthesis, Characterization, Antimicrobial Activity and Molecular Docking Studies of New Benzimidazole, Benzoxazole, Imidazole and Tetrazole Derivatives
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Synthesis, Characterization, Antimicrobial Activity and Molecular Docking Studies of New Benzimidazole, Benzoxazole, Imidazole and Tetrazole Derivatives

机译:新苯并咪唑,苯并恶唑,咪唑和四唑衍生物的合成,表征,抗菌活性和分子对接研究

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摘要

In the present research work, 12 new compounds, such as benzimidazole (3, 3a-c), benzoxazole(4), imidazole(5,5a-c) and tetrazole(6,6a-c) were synthesized. FT-IR, Proton NMR (1H), (13)~C-NMR, Mass spectral values were used to prove the structures of the compounds. The antimicrobial potential of the representative compounds was assessed using the Disc diffusion process. All the benzoxazole, benzimidazole, imidazole and tetrazole derivatives prepared in this investigation show good antimicrobial activity. However the antimicrobial activities of the compounds are less compared with standard drugs. Molecular docking studies have also done for the synthesized compounds all the compounds show hydrogen bond interactions with receptor protein.
机译:在本研究工作中,合成了12种新化合物,例如苯并咪唑(3,3a-C),苯并恶唑(4),咪唑(5,5A-C)和四唑(6,6A-C)。 FT-IR,质子NMR(1H),(13)〜C-NMR,质谱值用于证明化合物的结构。 使用盘扩散过程评估代表性化合物的抗微生物电位。 本研究中制备的所有苯并恶唑,苯并咪唑,咪唑和四唑衍生物显示出良好的抗微生物活性。 然而,与标准药物相比,化合物的抗微生物活性较少。 为合成化合物进行了分子对接研究,所有化合物都显示出与受体蛋白质的氢键相互作用。

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