作用机理
核酸
柔红霉素
拓扑异构酶
阿霉素
化学
药理学
药品
机制(生物学)
DNA
生物化学
生物
体外
化疗
遗传学
认识论
哲学
作者
Manish Shandilya,Shrutika Sharma,Prabhu Prasad Das,Sonika Charak
出处
期刊:IntechOpen eBooks
[IntechOpen]
日期:2020-11-06
被引量:15
标识
DOI:10.5772/intechopen.94180
摘要
Anthracyclines drugs are used as a treatment regime to combat cancer owing to their great chemotherapeutic potential. They are characterized by the presence of a wide range of derivatives, the most famous are doxorubicin and daunorubicin. The proposed action mechanism of anthracyclines and their derivatives to exert cytotoxic effect involves the intercalation of the drug molecule into nucleic acid and inhibition of the activity of topoisomerases. These events consequences in halting DNA replication and transcription mechanisms of the cell. Understanding of the structural and conformational changes associated with nucleic acid after binding with drugs provides significant knowledge for the development of more effective drugs. A comprehensive elucidation of the molecular mechanism(s) of action of anthracyclines drugs plays a significant role in the rational drug designing to obtain an effective, selective, and safe anti-cancer drugs.
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