半胱氨酸蛋白酶
合理设计
细胞凋亡
癌变
细胞毒性T细胞
细胞
坏死
癌症治疗
癌症
凋亡细胞死亡
生物
癌症研究
化学
程序性细胞死亡
生物化学
纳米技术
体外
材料科学
基因
遗传学
作者
Pelin Çıkla‐Süzgün,Ş. Güniz Küçükgüzel
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2021-02-10
卷期号:22 (16): 1844-1900
被引量:5
标识
DOI:10.2174/1389450122666210208181128
摘要
Apoptosis is often called programmed cell death and is defined as a self-directed cell destruction process. It is different from necrosis due to the activation of caspases during this process. Apoptosis is directly related to cancer progression and plays a vital role in carcinogenesis; all cytotoxic drugs and radiation therapy programs initiate apoptosis in tumor cells. Today, studies show that heterocyclic compounds that contain triazole functionality have anticancer activities; triazoles are 5- membered rings, which contain two carbon and three nitrogen atoms. Therefore, many researchers have synthesized these small active compounds as target structures and evaluated their apoptotic activities. The present review describes recent medicinal aspects of triazoles as anticancer agents that have been reported during the past few years. We hope that the bioactivity of triazole derivatives will be beneficial for the rational design of a new generation of small molecule drugs.
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