NAAG peptidase inhibitors and their potential for diagnosis and therapy

被引:191
作者
Zhou, J
Neale, JH
Pomper, MG
Kozikowski, AP
机构
[1] Acenta Discovery Inc, Tucson, AZ 85747 USA
[2] Georgetown Univ, Dept Biol, Washington, DC 20057 USA
[3] Johns Hopkins Univ, Dept Radiol, Baltimore, MD 21287 USA
[4] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Drug Discovery Program, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrd1903
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Modulation of N-acetyl-L-aspartyl-L-glutamate peptidase activity with small-molecule inhibitors holds promise for a wide variety of diseases that involve glutamatergic transmission, and has implications for the diagnosis and therapy of cancer. This new class of compounds, of which at least one has entered clinical trials and proven to be well tolerated, has demonstrated efficacy in experimental models of pain, schizophrenia, amyotrophic lateral sclerosis, traumatic brain injury and, when appropriately functionalized, can image prostate cancer. Further investigation of these promising drug candidates will be needed to bring them to the marketplace. The recent publication of the X-ray crystal structure for the enzymatic target of these compounds should facilitate the development of other new agents with enhanced activity that could improve both the diagnosis and treatment of neurological disorders.
引用
收藏
页码:1015 / 1026
页数:12
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