硫氧还蛋白还原酶
酶
硒蛋白
生物化学
硫氧还蛋白
化学
硒代半胱氨酸
药物发现
计算生物学
生物
半胱氨酸
谷胱甘肽
谷胱甘肽过氧化物酶
作者
Baoxin Zhang,Junmin Zhang,Shoujiao Peng,Ruijuan Liu,Xinming Li,Yanan Hou,Xiao Han,Jianguo Fang
标识
DOI:10.1080/13543776.2017.1272576
摘要
Mammalian thioredoxin reductases (TrxRs) are selenocysteine-containing homodimeric flavin enzymes that catalyze the NADPH-dependent reduction of oxidized thioredoxins. Increasing evidence indicates that TrxRs are potential targets for anticancer drug development. This review summarizes patented inhibitors of mammalian TrxRs with an emphasis on those having potential applications in treatment of cancer. Areas covered: A background introduction of TrxR as well as the relevance of TrxR and cancer is provided in the first part of this review. Then, a brief discussion of TrxR assays is followed in the second part. The patented TrxRs' inhibitors that were categorized into four classes, i. e., metal complexes, Michael acceptors, sulfur/selenium-containing compounds and others, are summarized in the third part of the review. Expert opinion: There is currently no clinical anticancer drug that specifically targets TrxR. One major hurdle in finding a successful TrxR inhibitor as a therapeutic drug is the specific inhibition of TrxR by an inhibitor. As most inhibitors described in literature and patents target the selenol group in the C-terminus of TrxR enzymes, it is hard to avoid cross interactions of such inhibitors with thiols. Novel strategies are proposed to achieve discovery of highly selective inhibitors of TrxR enzymes.
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