拓扑异构酶
化学
咪唑
药品
药物发现
微管
激酶
生物
计算生物学
药理学
DNA
生物化学
细胞生物学
作者
Salik Abdullah,Swastika Ganguly
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2023-09-01
卷期号:15 (17): 1621-1646
被引量:2
标识
DOI:10.4155/fmc-2023-0020
摘要
The quest for novel, physiologically active imidazoles remains an exciting topic of research among medicinal chemists. The imidazole ring is a five-membered aromatic heterocycle that is found in both natural and synthesized compounds. Multiple anticancer drug classes are currently available on the market, but concerns including toxicity, limited efficacy and solubility have lowered the overall therapeutic index. Therefore, the hunt for new potential chemotherapeutic agents persists. The development of imidazole as a reliable and safer alternative to anticancer treatment is generating much attention among experts. Tubulin or microtubule polymerization inhibition and changes in the structure and function of DNA, VEGF, topoisomerase, kinases, histone deacetylases and certain other proteins that affect gene expression are among the putative targets.
科研通智能强力驱动
Strongly Powered by AbleSci AI