新系列马来酰亚胺衍生物的设计、合成、生物学评价和分子对接研究。

IF 2.5 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Öznur Eyilcim, Fulya Günay, Yuk Yin Ng, Özlem Ulucan Açan, Zuhal Turgut, Ömer Tahir Günkara
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引用次数: 0

摘要

以各种杂环化合物作为侧链,合成了一系列新型马来酰亚胺衍生物。通过应用 1H-NMR 光谱、13C-NMR(APT)光谱和高分辨质谱法(HRMS),阐明了这些化合物的结构特征。随后,利用两种不同的乳腺癌细胞系(即 MDA-MB-231 和 MCF-7),通过 MTT 试验对这些化合物的抗癌潜力进行了体外评估。在这 12 个新合成的化合物中,4 a、4 b、4 c、4 d、5 a、5 b、5 c 和 5 d 被确定为对这两种乳腺癌细胞系具有最有希望的抗癌活性。此外,还利用光学显微镜观察了细胞在与这些化合物孵育 24 小时后发生的形态变化。此外,还进行了分子动力学模拟,以评估通过分子对接计算获得的化合物与靶蛋白 GSK-3β 结合构象的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design, Synthesis, Biological Evaluation and Molecular Docking Studies of a New Series of Maleimide Derivatives.

A series of novel maleimide derivatives were synthesized, with various heterocyclic compounds serving as side chains in the synthesis process. The structural characteristics of these compounds were elucidated through the application of 1H-NMR spectroscopy, 13C-NMR (APT) spectroscopy, and high-resolution mass spectrometry (HRMS). The anti-cancer potential of these compounds was subsequently assessed in vitro, utilizing two distinct breast cancer cell lines, namely MDA-MB-231 and MCF-7, via MTT assay. Among the 12 newly synthesized compounds, 4 a, 4 b, 4 c, 4 d, 5 a, 5 b, 5 c and 5 d were determined to show the most promising anti-cancer activity against both breast cancer cell lines. Moreover, the morphological changes induced in the cells following a 24-hour incubation period with these compounds were observed using light microscopy. Additionally, molecular dynamics simulations were conducted to assess the stability of the bound conformations of the compounds to the target protein GSK-3β as obtained through molecular docking calculations.

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来源期刊
ChemistryOpen
ChemistryOpen CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
4.80
自引率
4.30%
发文量
143
审稿时长
1 months
期刊介绍: ChemistryOpen is a multidisciplinary, gold-road open-access, international forum for the publication of outstanding Reviews, Full Papers, and Communications from all areas of chemistry and related fields. It is co-owned by 16 continental European Chemical Societies, who have banded together in the alliance called ChemPubSoc Europe for the purpose of publishing high-quality journals in the field of chemistry and its border disciplines. As some of the governments of the countries represented in ChemPubSoc Europe have strongly recommended that the research conducted with their funding is freely accessible for all readers (Open Access), ChemPubSoc Europe was concerned that no journal for which the ethical standards were monitored by a chemical society was available for such papers. ChemistryOpen fills this gap.
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