Synthesis, Characterization, In-Silico Docking Study and In-Vitro AntiInflammatory Activities of Novel Chalcone Derivatives

R. Bharathi, N. Santhi
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Abstract

A series of chalcones were synthesised by condensation of appropriate acetophenones with appropriate aromatic aldehydes, and their anti-inflammatory activities were investigated. In comparison to standard drugs, some have been found to have important activity. In silico docking, tests on chalcones were shown to be more selective to COX-2. Further anti-inflammatory results were supported by docking studies with COX-2. The results from the anti-inflammatory and docking indicate that the synthesised compounds 3b, 3g and 3h can be seen as therapeutic drugs.
新型查尔酮衍生物的合成、表征、硅对接研究及体外抗炎活性
通过适当的苯乙酮与适当的芳醛缩合反应,合成了一系列查尔酮,并对其抗炎活性进行了研究。与标准药物相比,有些已被发现具有重要的活性。在硅对接中,对查尔酮的测试显示对COX-2更具选择性。与COX-2的对接研究进一步支持了抗炎结果。抗炎和对接的结果表明,合成的化合物3b、3g和3h可视为治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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