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

硫氧还蛋白还原酶 硫氧还蛋白 硒蛋白 硒代半胱氨酸 化学 生物化学 还原酶 谷胱甘肽 药理学 生物 氧化应激 谷胱甘肽过氧化物酶 半胱氨酸
作者
Evgeny Chupakhin,Mikhail Krasavin
出处
期刊:Expert Opinion on Therapeutic Patents [Taylor & Francis]
卷期号:31 (8): 745-758 被引量:28
标识
DOI:10.1080/13543776.2021.1899160
摘要

Introduction: 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.Areas covered: 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.Expert opinion: 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.
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