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小分子Nrf2调节剂开发的最新进展:专利综述(2012 - 2016年)

Recent progress in the development of small molecule Nrf2 modulators: a patent review (2012-2016).

作者信息

Sun Haopeng, Zhu Jie, Lin Hongzhi, Gu Kai, Feng Feng

机构信息

a Department of Medicinal Chemistry , China Pharmaceutical University , Nanjing , China.

b Key Laboratory of Biomedical Functional Materials, School of Science , China Pharmaceutical University , Nanjing , China.

出版信息

Expert Opin Ther Pat. 2017 Jul;27(7):763-785. doi: 10.1080/13543776.2017.1325464. Epub 2017 May 10.

DOI:10.1080/13543776.2017.1325464
PMID:28454500
Abstract

The NF-E2-related factor-2 (Nrf2) is a critical transcription factor that regulates the expression of many phase II and antioxidant genes to maintain the homeostasis. It has many biological functions and plays a central role in the cellular defensive machinery. The abnormal regulation of Nrf2 is closely associated with multiple diseases. Areas covered: This article first discusses the molecular regulatory mechanism of Nrf2-antioxidant response element (ARE) signaling. Then patents and publications about Nrf2 activators and inhibitors from 2012-2016 are reviewed. Several case studies are emphasized to introduce the molecular design strategy, especially on Keap1-Nrf2 protein-protein interaction (PPI) inhibitor. Expert opinion: Firstly, new chemotypes of Nrf2 modulators can be designed in a combination of the progress of both covalent modifiers and target selective Keap1-Nrf2 interaction inhibitors. The aim is to balance the activity and toxicity of Nrf2 modulators. Secondly, considering many known Nrf2 activators, such as DMF and SFN, are electrophilic entities with very small molecular weight, we need to update the concept of how to recognize a drug candidate. Finally, per the mechanism of the Nrf2 modulator, compounds with the most active Nrf2 inductivity maybe not the best choice for the design of an ideal chemopreventive agent.

摘要

核因子E2相关因子2(Nrf2)是一种关键的转录因子,它调节许多II期和抗氧化基因的表达以维持体内平衡。它具有多种生物学功能,在细胞防御机制中发挥核心作用。Nrf2的异常调节与多种疾病密切相关。涵盖领域:本文首先讨论Nrf2-抗氧化反应元件(ARE)信号通路的分子调节机制。然后综述了2012年至2016年关于Nrf2激活剂和抑制剂的专利及出版物。强调了几个案例研究以介绍分子设计策略,特别是关于Keap1-Nrf2蛋白-蛋白相互作用(PPI)抑制剂。专家观点:首先,可以结合共价修饰剂和靶向选择性Keap1-Nrf2相互作用抑制剂的进展来设计Nrf2调节剂的新化学类型。目的是平衡Nrf2调节剂的活性和毒性。其次,考虑到许多已知的Nrf2激活剂,如DMF和SFN,是分子量非常小的亲电实体,我们需要更新如何识别候选药物的概念。最后,根据Nrf2调节剂的作用机制,具有最高活性Nrf2诱导能力的化合物可能不是设计理想化学预防剂的最佳选择。

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