奥西多尔
吲哚试验
药物发现
小分子
纳米技术
计算生物学
抗癌药
化学
医学
药品
生物
生物信息学
药理学
生物化学
材料科学
催化作用
作者
Xiang Li,Yanqing Liu,Wei Huang,Xin Xie,Hongping Zhu,Cheng Peng,Bo Han
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2023-06-01
卷期号:23 (10): 1164-1173
标识
DOI:10.2174/1871520622666220509175305
摘要
: Indole and spiro-fused oxindole frameworks widely exist in a variety of natural bioactive products, pharmaceuticals, and drug candidates, featuring unique functions in the regulation of proliferation, infiltration, and metastasis of cancer cells. In recent years, significant progress in proteolysis targeting chimeric (PROTAC) technology that employs ubiquitin-proteasome system (UPS) to eliminate disease-associated proteins has been witnessed, thus opening a promising avenue to the discovery of new indole-related drugs. : In this review, we focus on summarizing the achievements of small molecule PROTACs that involve indole/spirofused oxindole scaffolds in the part of ligands of the protein of interest (POI). Current challenges and future directions in this promising field are discussed at the end of this review. For the convenience of readers, our review is divided into five parts according to the types of target proteins. We hope this review could bring a quick look and some inspiration to researchers in relevant fields.
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