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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Proteolysis targeting chimera (PROTAC) in drug discovery paradigm: Recent progress and future challenges
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Proteolysis targeting chimera (PROTAC) in drug discovery paradigm: Recent progress and future challenges

机译:蛋白水解靶向嵌合体(Protac)在药物发现范式中:最近的进展和未来的挑战

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摘要

Proteolysis targeting chimera (PROTAC), hijacking protein of interest (POI) and recruiting E3 ligase for target degradation via the ubiquitin-proteasome pathway, is a novel drug discovery paradigm which has been widely used as biological tools and medicinal molecules with the potential of clinical application value. Currently, ARV-110, an orally small molecule PROTAC was designed to specifically target Androgen receptor (AR), firstly enters clinical phase I trials for the treatment of metastatic castration-resistant prostate cancer, which turns a new avenue for the development of PROTAC. We herein provide a detail summary on the latest one year progress of PROTAC target various proteins and elucidate the advantages of PROTAC technology. Finally, the potential challenges of this vibrant field are also discussed. (C) 2020 Elsevier Masson SAS. All rights reserved.
机译:蛋白质水解靶向嵌合体(PROTAC)是通过泛素-蛋白酶体途径劫持感兴趣蛋白(POI)并招募E3连接酶进行靶向降解的一种新的药物发现范式,已被广泛用作生物工具和药物分子,具有潜在的临床应用价值。目前,ARV-110是专门针对雄激素受体(AR)设计的口服小分子PROTAC,首次进入治疗转移性去势抵抗前列腺癌的临床I期试验,为PROTAC的开发开辟了新途径。本文详细总结了PROTAC靶向各种蛋白质一年来的最新进展,并阐明了PROTAC技术的优势。最后,还讨论了这一充满活力的领域的潜在挑战。(C) 2020年爱思唯尔马森SAS。版权所有。

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