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硫氧还蛋白还原酶抑制剂:更新的专利审查(2017 年至今)。

Thioredoxin reductase inhibitors: updated patent review (2017-present).

机构信息

Institute of Chemistry, Saint Petersburg State University, Saint Petersburg Russian Federation.

Institute for Living Systems, Immanuel Kant Baltic Federal University, Kaliningrad Russian Federation.

出版信息

Expert Opin Ther Pat. 2021 Aug;31(8):745-758. doi: 10.1080/13543776.2021.1899160. Epub 2021 Mar 22.

DOI:10.1080/13543776.2021.1899160
PMID:33666133
Abstract

: Thioredoxin reductase (TrxR) is a selenocysteine-containing enzyme which is responsible - as a part of the thioredoxin system - for maintaining redox homeostasis in cells. It is upregulated in cancerous state as a defense against oxidative stress. TrxR has been mostly considered an anticancer drug target although it has applications in other therapeutic areas such as neurodegeneration, inflammation, microbial infections, and neonatal hyperoxic lung injury.: The present review covers the patent literature that appeared in the period 2017-2020, i.e. since the publication of the previous expert opinion patent review on TrxR inhibitors. The recent additions to the following traditional classes of inhibitors are discussed: metal complexes, Michael acceptors as well as arsenic and selenium compounds. At the same time, a novel group of nitro (hetero)aromatic compounds have emerged which likely acts via covalent inhibition mechanism. Several miscellaneous chemotypes are grouped under Miscellaneous subsection.: While specificity over glutathione reductase is achieved easily, TrxR is still moving toward the later stages of development at a very slow rate. Michael acceptors, particularly based on TRXR substrate-mimicking scaffolds, are gaining impetus and so are dual and hybrid compounds. The development prospects of the emerging nitro (hetero)aromatic chemotypes remain uncertain.

摘要

硫氧还蛋白还原酶(TrxR)是一种含硒半胱氨酸的酶,作为硫氧还蛋白系统的一部分,负责维持细胞内的氧化还原平衡。在癌变状态下,它被上调,作为抵御氧化应激的一种防御机制。尽管 TrxR 在神经退行性疾病、炎症、微生物感染和新生儿高氧肺损伤等其他治疗领域也有应用,但它主要被认为是一种抗癌药物靶点。

本综述涵盖了 2017 年至 2020 年期间发表的专利文献,即自上次关于 TrxR 抑制剂的专家意见专利综述出版以来。讨论了以下传统抑制剂类别的最新进展:金属配合物、迈克尔受体以及砷和硒化合物。同时,出现了一类新型的硝基(杂)芳族化合物,它们可能通过共价抑制机制发挥作用。几种杂类化学型被归为杂项部分。

虽然很容易实现对谷胱甘肽还原酶的特异性,但 TrxR 的开发仍然非常缓慢,处于后期阶段。迈克尔受体,特别是基于 TRXR 底物模拟支架的迈克尔受体,正在获得动力,双和杂合化合物也是如此。新兴的硝基(杂)芳族化学型的发展前景仍不确定。

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