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新型吡唑-苯并咪唑衍生物的设计、合成及体外抗肿瘤活性评价。

Design, synthesis and in vitro antitumor evaluation of novel pyrazole-benzimidazole derivatives.

机构信息

Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling, 712100 Shaanxi, PR China.

Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling, 712100 Shaanxi, PR China.

出版信息

Bioorg Med Chem Lett. 2021 Jul 1;43:128097. doi: 10.1016/j.bmcl.2021.128097. Epub 2021 May 9.

Abstract

A series of novel pyrazole-benzimidazole derivatives (6-42) have been designed, synthesized and evaluated for their in vitro antiproliferative activity against the HCT116, MCF-7 and Huh-7 cell lines. Among them, compounds 17, 26 and 35 showed significant antiproliferative activity against HCT116 cell lines with the IC values of 4.33, 5.15 and 4.84 μM, respectively. Moreover, fluorescent staining studies showed compound 17 could induce cancer cells apoptosis. The flow cytometry assay revealed that compound 17 could induce cell cycle arrest at G0/G1 phase. All in all, these consequences suggest that pyrazole-benzimidazole derivatives could serve as promising compounds for further research to develop novel and highly potent cancer therapy agents.

摘要

一系列新型吡唑并苯并咪唑衍生物(6-42)被设计、合成并评估了它们对 HCT116、MCF-7 和 Huh-7 细胞系的体外增殖活性。其中,化合物 17、26 和 35 对 HCT116 细胞系表现出显著的增殖活性,IC 值分别为 4.33、5.15 和 4.84 μM。此外,荧光染色研究表明,化合物 17 能够诱导癌细胞凋亡。流式细胞术检测显示,化合物 17 能够诱导细胞周期停滞在 G0/G1 期。总之,这些结果表明,吡唑并苯并咪唑衍生物可能是进一步研究开发新型高效抗癌药物的有前途的化合物。

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