Small-molecule arginase inhibitors

被引:0
作者
Ivanenkov, Yan A. [1 ,2 ]
Chufarova, Nina V. [1 ]
机构
[1] State Univ, Moscow Inst Phys & Technol, 9 Inst Skiy Lane, Dolgoprudny City 141700, Moscow Region, Russia
[2] ChemDiv, 6605 Nancy Ridge Dr, San Diego, CA 92121 USA
关键词
D O I
10.4155/PPA.13.75
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Arginase is an enzyme that metabolizes l-arginine to l-ornithine and urea. In addition to its fundamental role in the hepatic ornithine cycle, it also influences the immune systems in humans and mice. Arginase participates in many inflammatory disorders by decreasing the synthesis of nitric oxide and inducing fibrosis and tissue regeneration. l-arginine deficiency, which is modulated by myeloid cell arginase, suppresses T-cell immune response. This mechanism plays a fundamental role in inflammation-associated immunosuppression. Pathogens can synthesize their own arginase to elude immune reaction. Small-molecule arginase inhibitors are currently described as promising therapeutics for the treatment of several diseases, including allergic asthma, inflammatory bowel disease, ulcerative colitis, cardiovascular diseases (atherosclerosis and hypertension), diseases associated with pathogens (e.g., Helicobacter pylori, Trypanosoma cruzi, Leishmania, Mycobacterium tuberculosis and Salmonella), cancer and induced or spontaneous immune disorders. This article summarizes recent patents in the area of arginase inhibitors and discusses their properties.
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页码:65 / 85
页数:21
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