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探索新型吲唑衍生物作为 ASK1 抑制剂:设计、合成、生物评价及对接研究。

Exploring novel indazole derivatives as ASK1 inhibitors: Design, synthesis, biological evaluation and docking studies.

机构信息

College of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang 330004, PR China.

Fujian Provincial Key Laboratory of Hepatic Drug Research, Ningde 355300, PR China.

出版信息

Bioorg Chem. 2024 Jun;147:107391. doi: 10.1016/j.bioorg.2024.107391. Epub 2024 Apr 22.

Abstract

Apoptosis signal regulated kinase 1 (ASK1, MAP3K5) is a member of the mitogen activated protein kinase (MAPK) signaling pathway, involved in cell survival, differentiation, stress response, and apoptosis. ASK1 kinase inhibition has become a promising strategy for the treatment of Non-alcoholic steatohepatitis (NASH) disease. A series of novel ASK1 inhibitors with indazole scaffolds were designed and synthesized, and their ASK1 kinase activities were evaluated. The System Structure Activity Relationship (SAR) study discovered a promising compound 33c, which has a strong inhibitory effect on ASK1. Noteworthy observations included a discernible reduction in lipid droplets within LO2 cells stained with Oil Red O, coupled with a decrease in LDL, CHO, and TG content within the NASH model cell group. Mechanistic inquiries revealed that compound 33c could inhibit the protein expression levels of the upregulated ASK1-p38/JNK signaling pathway in TNF-α treated HGC-27 cells and regulate apoptotic proteins. In summary, these findings suggest that compound 33c may be valuable for further research as a potential candidate compound against NASH.

摘要

凋亡信号调节激酶 1(ASK1,MAP3K5)是丝裂原活化蛋白激酶(MAPK)信号通路的成员,参与细胞存活、分化、应激反应和细胞凋亡。ASK1 激酶抑制已成为治疗非酒精性脂肪性肝炎(NASH)疾病的一种有前途的策略。设计并合成了一系列具有吲唑骨架的新型 ASK1 抑制剂,并对其 ASK1 激酶活性进行了评估。系统结构活性关系(SAR)研究发现了一种有前途的化合物 33c,它对 ASK1 具有很强的抑制作用。值得注意的观察结果包括用油红 O 染色的 LO2 细胞内脂滴明显减少,同时 NASH 模型细胞组内 LDL、CHO 和 TG 含量降低。机制研究表明,化合物 33c 可以抑制 TNF-α处理的 HGC-27 细胞中上调的 ASK1-p38/JNK 信号通路的蛋白表达水平,并调节凋亡蛋白。总之,这些发现表明,化合物 33c 可能是一种有价值的研究工具,可作为治疗 NASH 的潜在候选化合物。

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