噻唑类腙衍生物的合成、计算、溶剂化变色及生物学研究

Q4 Materials Science
C. K. Yadav, B. Nandeshwarappa, K. Mussuvir Pasha
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引用次数: 1

摘要

在本工作中,我们合成了噻唑腙偶联物5(a–h),并使用各种分析技术(如UV、IR、NMR和质谱)对其进行了表征。使用DFT研究在具有不同极性和量子化学参数的十种溶剂中评估了溶剂致变色性质。抗菌活性结果表明,化合物5c、5d和5g表现出良好的抗菌效果,其余化合物表现出显著的抗菌活性。筛选合成的化合物对HepG2和MCF-7细胞系的细胞毒性活性,所有合成的化合物都对筛选的癌症细胞系表现出显著的效力。测定了合成的噻唑衍生物对MMP-2和MMP-9的抗炎作用,并且一些化合物显示出显著的活性。此外,用COX-2受体进行了计算机分子对接。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, computational study, solvatochromism and biological studies of thiazole-owing hydrazone derivatives
In the present work, we have synthesized thiazole-hydrazone conjugates 5(a–h) and characterized them using various analytical techniques such as UV, IR, NMR, and mass spectrometry. Solvatochromic properties were evaluated in ten solvents with different polarity and quantum chemical parameters using a DFT study. The antibacterial activity results revealed that compounds 5c, 5d and 5g exhibited good efficacy and that the remaining compounds displayed significant activity. The synthesized compounds were screened for their cytotoxic activity against HepG2 and MCF-7 cell lines, and all the synthesized compounds exhibited significant potency towards the screened cancer cell lines. The anti-inflammatory efficacy of the synthesized thiazole derivatives was determined against MMP-2 and MMP-9, and some of the compounds showed significant activity. Furthermore, the in silico molecular docking was performed with the COX-2 receptor.
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来源期刊
Chimica Techno Acta
Chimica Techno Acta Chemical Engineering-Chemical Engineering (all)
CiteScore
1.00
自引率
0.00%
发文量
67
审稿时长
4 weeks
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