Khan Javed A, Forouhar Farhad, Tao Xiao, Tong Liang
Columbia University, Department of Biological Sciences, New York, NY 10027, USA.
Expert Opin Ther Targets. 2007 May;11(5):695-705. doi: 10.1517/14728222.11.5.695.
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.
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。