吲哚试验
长春碱
体内
体外
药理学
计算生物学
生物化学
生物
化学
医学
生物技术
化疗
内科学
作者
Anuradha Mehra,Vikas Sharma,Anil Verma,Sneha Venugopal,Amit Mittal,Gurdeep Singh,Balwinder Kaur
标识
DOI:10.1002/slct.202202361
摘要
Abstract Indole moiety is a magnificent nucleus in the development of anticancer drugs. The pharmacological profile of indole is excellent in targeting a wide range of proteins, enzymes. An indole has a nitrogen atom that is capable of forming hydrogen bonds with the targets emphasizing its potential. Many studies have demonstrated the effectiveness of indole in the treatment of cancer by working through various pathways. Indole‐based drugs got market approval to be used as chemotherapeutics, such as vincristine and vinblastine which encourage researchers to work on indole derivatives for cancer treatment with a better pharmacokinetic profile. This prompted us to review on indole derivatives as anticancer agents to bring out their potential derivatives under study. This study encompasses literature published between 2014 and 2021 on indole scaffold that exhibits in vitro and in vivo potential against cancer by searching PubMed, Google Scholar, and Science Direct databases. The search terms were “anticancer”, “indole”, “cell lines”, “structure‐activity relationship” and “cytotoxic activity.”
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