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Synthesis and Characterization of 2-Pyrazoline Derivatives and their in silico and in vitro Studies on Antimicrobial and Anticancer Activities

机译:二吡唑啉衍生物的合成与表征及其在抗微生物和抗癌活动中的体外研究

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摘要

The new series of 1-(4,5-dihydro-5-phenyl-3-diphenylpyrazol-l-yl)butan-l-one derivatives were synthesized by cyclization method using biphenyl chalcone with n-butyric acid and hydrazine hydrate. The synthesized l-(4,5-dihydro-5-phenyl-3-diphenylpyrazol-l-yl)butan-l-one derivatives chemical strucmres were confirmed from spectral data such as FT-IR, 'H and 13C NMR. 2-Pyrazoline derivatives were docked with bacterial (1UAG) and breast cancer (10QA) protein. Based on high binding affinity score, the best compound was subjected to in vitro anticancer activity by MTT assay. Also, antimicrobial activity were studied for synthesized 2-pyrazoline derivatives.
机译:通过使用具有正丁酸和肼水合物的联苯醌和肼水合物,通过环化方法合成了新的1-(4,5-二氢-5-苯基-3-二苯基吡唑-1-基-1-炔胺的新系列丁烷-1-一种衍生物。 合成的L-(4,5-二氢-5-苯基-3-二苯基吡唑-1-基)从诸如FT-IR,H和13C NMR等光谱数据证实了Butan-L-One衍生物化学曲率。 将2-吡唑啉衍生物与细菌(1UAG)和乳腺癌(10QA)蛋白停靠。 基于高结合亲和力评分,通过MTT测定对最佳化合物进行体外抗癌活性。 此外,研究了合成的2-吡唑啉衍生物的抗微生物活性。

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