吲哚试验
化学
药效团
吡咯
部分
戒指(化学)
组合化学
双环分子
拓扑异构酶
立体化学
生物化学
酶
有机化学
作者
Reyaz Hassan Mir,Roohi Mohi-ud-din,Taha Umair Wani,Mohammad Ovais Dar,Abdul Jalil Shah,Bashir A. Lone,Pooja A. Chawla,Mubashir Hussain Masoodi
标识
DOI:10.2174/1385272825666210208142108
摘要
Heterocyclic are a class of compounds that are intricately entwined into life processes. Almost more than 90% of marketed drugs carry heterocycles. Synthetic chemistry, in turn, allocates a cornucopia of heterocycles. Among the heterocycles, indole, a bicyclic structure consisting of a six-membered benzene ring fused to a five-membered pyrrole ring with numerous pharmacophores that generate a library of various lead molecules. Due to its profound pharmacological profile, indole got wider attention around the globe to explore it fully in the interest of mankind. The current review covers recent advancements on indole in the design of various anti-cancer agents acting by targeting various enzymes or receptors, including (HDACs), sirtuins, PIM kinases, DNA topoisomerases, and σ receptors.
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