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Bioorg Chem. 2024 Apr;145:107235. doi: 10.1016/j.bioorg.2024.107235. Epub 2024 Feb 20.
3
Design, synthesis, antitumor evaluation, and molecular docking of novel pyrrolo[2,3-d]pyrimidine as multi-kinase inhibitors.新型吡咯并[2,3-d]嘧啶作为多激酶抑制剂的设计、合成、抗肿瘤评估及分子对接
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J Med Chem. 2023 Jan 26;66(2):1112-1136. doi: 10.1021/acs.jmedchem.2c01606. Epub 2023 Jan 16.
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5-羟基苯并噻吩衍生物的开发作为具有潜在抗癌活性的多激酶抑制剂。

Development of 5-hydroxybenzothiophene derivatives as multi-kinase inhibitors with potential anti-cancer activity.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy & Biotechnology, German University in Cairo, Cairo, 11835, Egypt.

Department of Medical Research, E-Da Hospital, I-Shou University, Kaohsiung, 824410, Taiwan.

出版信息

Future Med Chem. 2024;16(12):1239-1254. doi: 10.1080/17568919.2024.2342708. Epub 2024 May 22.

DOI:10.1080/17568919.2024.2342708
PMID:38989990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11249150/
Abstract

Chemoresistance in cancer challenges the classical therapeutic strategy of 'one molecule-one target'. To combat this, multi-target therapies that inhibit various cancer-relevant targets simultaneously are proposed. We introduce 5-hydroxybenzothiophene derivatives as effective multi-target kinase inhibitors, showing notable growth inhibitory activity across different cancer cell lines. Specifically, compound , featuring a 5-hydroxybenzothiophene hydrazide scaffold, emerged as a potent inhibitor, displaying low IC values against key kinases and demonstrating significant anti-cancer effects, particularly against U87MG glioblastoma cells. It induced G2/M cell cycle arrest, apoptosis and inhibited cell migration by modulating apoptotic markers. represents a promising lead for developing new anti-cancer agents targeting multiple kinases with affinity to the hydroxybenzothiophene core.

摘要

癌症的化学抗性对“一个分子,一个靶点”的经典治疗策略提出了挑战。为了应对这一挑战,人们提出了同时抑制多种与癌症相关靶点的多靶点治疗方法。

我们介绍了 5-羟基苯并噻吩衍生物作为有效的多靶点激酶抑制剂,在不同的癌细胞系中表现出显著的生长抑制活性。具体来说,化合物 ,具有 5-羟基苯并噻吩酰肼骨架,是一种有效的抑制剂,对关键激酶的 IC 值较低,并表现出显著的抗癌作用,特别是对 U87MG 神经胶质瘤细胞。它通过调节凋亡标志物诱导 G2/M 细胞周期停滞、细胞凋亡和抑制细胞迁移。 代表了一种有前途的先导化合物,可用于开发针对多种激酶的新型抗癌药物,对羟基苯并噻吩核心具有亲和力。