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新型马来酰亚胺衍生物系列的设计、合成、生物学评价及分子对接研究

Design, Synthesis, Biological Evaluation and Molecular Docking Studies of a New Series of Maleimide Derivatives.

作者信息

Eyilcim Öznur, Günay Fulya, Ng Yuk Yin, Ulucan Açan Özlem, Turgut Zuhal, Günkara Ömer Tahir

机构信息

Department of Chemistry, Faculty of Arts & Science, Yıldız Technical University, Davutpaşa Campus, 34220, Esenler, Istanbul, Türkiye.

Food Technology Programme, Vocational School of Health Services, Üsküdar University, Carsi Campus, Üsküdar, Istanbul, Türkiye.

出版信息

ChemistryOpen. 2024 Dec;13(12):e202400058. doi: 10.1002/open.202400058. Epub 2024 Sep 23.

DOI:10.1002/open.202400058
PMID:39313991
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11625963/
Abstract

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 H-NMR spectroscopy, C-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.

摘要

合成了一系列新型马来酰亚胺衍生物,在合成过程中使用了各种杂环化合物作为侧链。通过应用氢核磁共振光谱、碳核磁共振(APT)光谱和高分辨率质谱(HRMS)对这些化合物的结构特征进行了阐明。随后,利用MTT法,在体外使用两种不同的乳腺癌细胞系,即MDA-MB-231和MCF-7,评估了这些化合物的抗癌潜力。在12种新合成的化合物中,确定4 a、4 b、4 c、4 d、5 a、5 b、5 c和5 d对两种乳腺癌细胞系均显示出最有前景的抗癌活性。此外,使用光学显微镜观察了用这些化合物孵育24小时后细胞中诱导的形态变化。另外,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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/c12d0c22397b/OPEN-13-e202400058-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/76006c655e15/OPEN-13-e202400058-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/adcd03a2e5a8/OPEN-13-e202400058-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/4d89c75fb9d7/OPEN-13-e202400058-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/fea12f90e60b/OPEN-13-e202400058-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/d4b65b3409d6/OPEN-13-e202400058-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/2323d39f113e/OPEN-13-e202400058-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/23f1c6879829/OPEN-13-e202400058-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/c12d0c22397b/OPEN-13-e202400058-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/76006c655e15/OPEN-13-e202400058-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/adcd03a2e5a8/OPEN-13-e202400058-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/4d89c75fb9d7/OPEN-13-e202400058-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/fea12f90e60b/OPEN-13-e202400058-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/d4b65b3409d6/OPEN-13-e202400058-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/2323d39f113e/OPEN-13-e202400058-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/23f1c6879829/OPEN-13-e202400058-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4318/11625963/c12d0c22397b/OPEN-13-e202400058-g009.jpg

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