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基于靶点的抗癌吲哚衍生物及其构效关系洞察:机制综述更新(2018 - 2021年)

Target-based anticancer indole derivatives and insight into structure‒activity relationship: A mechanistic review update (2018-2021).

作者信息

Dhiman Ashima, Sharma Rupam, Singh Rajesh K

机构信息

Department of Pharmaceutical Chemistry, Shivalik College of Pharmacy, IKG Punjab Technical University, Jalandhar 140126, India.

出版信息

Acta Pharm Sin B. 2022 Jul;12(7):3006-3027. doi: 10.1016/j.apsb.2022.03.021. Epub 2022 Apr 1.

Abstract

Cancer, which is the uncontrolled growth of cells, is the second leading cause of death after heart disease. Targeting drugs, especially to specific genes and proteins involved in growth and survival of cancer cells, is the prime need of research world-wide. Indole moiety, which is a combination of aromatic-heterocyclic compounds, is a constructive scaffold for the development of novel leads. Owing to its bioavailability, high unique chemical properties and significant pharmacological behaviours, indole is considered as the most inquisitive scaffold for anticancer drug research. This is illustrated by the fact that the U.S. Food and Drug Administration (FDA) has recently approved several indole-based anticancer agents such as panobinostat, alectinib, sunitinib, osimertinib, anlotinib and nintedanib for clinical use. Furthermore, hundreds of studies on the synthesis and activity of the indole ring have been published in the last three years. Taking into account the facts stated above, we have presented the most recent advances in medicinal chemistry of indole derivatives, encompassing hot articles published between 2018 and 2021 in anticancer drug research. The recent advances made towards the synthesis of promising indole-based anticancer compounds that may act various targets such as topoisomerase, tubulin, apoptosis, aromatase, kinases, etc., have been discussed. This review also summarizes some of the recent efficient green chemical synthesis for indole rings using various catalysts for the period during 2018-2021. The review also covers the synthesis, structure‒activity relationship, and mechanism by which these leads have demonstrated improved and promising anticancer activity. Indole molecules under clinical and preclinical stages are classified into groups based on their cancer targets and presented in tabular form, along with their mechanism of action. The goal of this review article is to point the way for medicinal chemists to design and develop effective indole-based anticancer agents.

摘要

癌症是细胞的无节制生长,是仅次于心脏病的第二大死因。靶向药物,尤其是针对参与癌细胞生长和存活的特定基因和蛋白质的药物,是全球研究的首要需求。吲哚部分是一种芳香杂环化合物的组合,是开发新型先导化合物的建设性支架。由于其生物利用度、独特的化学性质和显著的药理行为,吲哚被认为是抗癌药物研究中最具探索性的支架。美国食品药品监督管理局(FDA)最近批准了几种基于吲哚的抗癌药物,如帕比司他、阿来替尼、舒尼替尼、奥希替尼、安罗替尼和尼达尼布用于临床,这一事实就说明了这一点。此外,在过去三年里,已经发表了数百篇关于吲哚环合成和活性的研究。考虑到上述事实,我们介绍了吲哚衍生物药物化学的最新进展,包括2018年至2021年发表的关于抗癌药物研究的热门文章。讨论了在合成有前景的基于吲哚的抗癌化合物方面取得的最新进展,这些化合物可能作用于各种靶点,如拓扑异构酶、微管蛋白、凋亡、芳香化酶、激酶等。本综述还总结了2018 - 2021年期间使用各种催化剂对吲哚环进行的一些最新高效绿色化学合成。该综述还涵盖了这些先导化合物表现出改善和有前景的抗癌活性的合成、构效关系和作用机制。处于临床和临床前阶段的吲哚分子根据其癌症靶点进行分类,并以表格形式呈现,同时列出其作用机制。这篇综述文章的目的是为药物化学家设计和开发有效的基于吲哚的抗癌药物指明方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7171/9293743/3807e8cb3978/ga1.jpg

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