Anticancer agents incorporating the N-acylhydrazone scaffold: Progress from 2017 to present

被引:9
作者
Kassab, Asmaa E. [1 ,2 ]
机构
[1] Cairo Univ, Fac Pharm, Dept Pharmaceut Organ Chem, Cairo, Egypt
[2] Cairo Univ, Fac Pharm, Dept Pharmaceut Organ Chem, 33 Kasr El Aini St, Cairo 11562, Egypt
关键词
anticancer; apoptosis; caspases; N-acylhydrazone; structure-activity relationship; BIOLOGICAL EVALUATION; PHARMACOLOGICAL EVALUATION; PROCASPASE-3; ACTIVATION; COX-2; INHIBITORS; IN-VITRO; DERIVATIVES; DESIGN; CANCER; DRUG; APOPTOSIS;
D O I
10.1002/ardp.202200548
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The N-acylhydrazone motif has been shown to be particularly adaptable and promising in the area of medicinal chemistry and drug development, due to its significant biological and pharmacological characteristics. Moreover, N-acylhydrazones are appealing synthetic and biological tools because of their simple and straightforward synthesis. This scaffold has emerged as a fundamental building block for the synthesis of bioactive compounds. Particularly, the N-acylhydrazone scaffold served as a base for the synthesis of a number of potent anticancer agents acting via different mechanisms. An updated summary of the anticancer activity of N-acylhydrazone derivatives described in the literature (from 2017 to 2022) is provided in the current review. It discusses the structure-activity relationship (SAR) of N-acylhydrazone derivatives exhibiting anticancer potential, which could be helpful in designing and developing new derivatives as effective antiproliferative candidates in the future.
引用
收藏
页数:22
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