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烟酰胺腺嘌呤二核苷酸代谢作为药物研发的一个有吸引力的靶点。

Nicotinamide adenine dinucleotide metabolism as an attractive target for drug discovery.

作者信息

Khan Javed A, Forouhar Farhad, Tao Xiao, Tong Liang

机构信息

Columbia University, Department of Biological Sciences, New York, NY 10027, USA.

出版信息

Expert Opin Ther Targets. 2007 May;11(5):695-705. doi: 10.1517/14728222.11.5.695.

Abstract

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.

摘要

烟酰胺腺嘌呤二核苷酸(NAD(+))在许多细胞过程中发挥着关键作用,既是氧化还原反应的辅酶,又是捐赠ADP - 核糖单元的底物。参与NAD(+)代谢的酶是针对多种人类疾病(包括癌症、多发性硬化症、神经退行性变和亨廷顿舞蹈症)进行药物研发的有吸引力的靶点。烟酰胺磷酸核糖转移酶是NAD(+)生物合成补救途径中的一种酶,其小分子抑制剂目前正在进行抗癌临床试验。犬尿氨酸途径中间体的类似物在动物模型中对多发性硬化症有效。吲哚胺2,3 - 双加氧酶在癌细胞免疫逃逸和其他疾病过程中起重要作用。针对犬尿氨酸3 - 羟化酶的抑制剂可减少神经毒性代谢物的产生,同时增加神经保护化合物的产生。本综述总结了关于NAD(+)代谢酶的现有知识,重点在于它们与药物研发的相关性。

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