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首页> 外文期刊>Expert opinion on therapeutic targets >Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery.
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Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery.

机译:烟酰胺腺嘌呤二核苷酸代谢作为药物发现的有吸引力的目标。

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摘要

Nicotinamide adenine dinucleotide (NAD(+)) has crucial roles in many cellular processes, both as a coenzyme for redox reactions and as a substrate to donate ADP-ribose units. Enzymes involved in NAD(+) metabolism are attractive targets for drug discovery against a variety of human diseases, including cancer, multiple sclerosis, neurodegeneration and Huntington's disease. A small-molecule inhibitor of nicotinamide phosphoribosyltransferase, an enzyme in the salvage pathway of NAD(+) biosynthesis, is presently in clinical trials against cancer. An analog of a kynurenine pathway intermediate is efficacious against multiple sclerosis in an animal model. Indoleamine 2,3-dioxygenase plays an important role in immune evasion by cancer cells and other disease processes. Inhibitors against kynurenine 3-hydroxylase can reduce the production of neurotoxic metabolites while increasing the production of neuroprotective compounds. This review summarizes the existing knowledge on NAD(+) metabolic enzymes, with emphasis on their relevance for drug discovery.
机译:烟酰胺腺嘌呤二核苷酸(NAD(+))在许多细胞过程中都起着至关重要的作用,既是氧化还原反应的辅酶,又是捐赠ADP核糖单位的基质。涉及NAD(+)代谢的酶是针对多种人类疾病(包括癌症,多发性硬化症,神经退行性疾病和亨廷顿氏病)的药物开发的有吸引力的目标。烟酰胺磷酸核糖基转移酶的一种小分子抑制剂,是NAD(+)生物合成挽救途径中的一种酶,目前正在抗癌的临床试验中。犬尿氨酸途径中间体的类似物对动物模型中的多发性硬化有效。吲哚胺2,3-二加氧酶在癌细胞和其他疾病过程的免疫逃逸中起重要作用。犬尿氨酸3-羟化酶的抑制剂可以减少神经毒性代谢产物的产生,同时增加神经保护化合物的产生。这篇综述总结了有关NAD(+)代谢酶的现有知识,重点是它们与药物发现的相关性。

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