Brown Stephen, Meroueh Samy O, Fridman Rafael, Mobashery Shahriar
Department of Chemistry and Biochemistry, 423 Nieuwland Science Center, University of Notre Dame, IN 46556, USA.
Curr Top Med Chem. 2004;4(12):1227-38. doi: 10.2174/1568026043387854.
Matrix metalloproteinases (MMPs), of which at least 26 are known in humans, have been linked to a number of pathological conditions including tumor metastasis, inflammation, neurological and cardiovascular diseases. Inhibition of MMPs has been widely sought as a strategy in intervention of these disease processes. Whereas a large number of broad-spectrum MMP inhibitors have been developed over the past decade, these inhibitors have not met the promise and expectations in clinical trials. The broad-spectrum inhibition, which besides MMPs often targets other metalloproteinases, has been considered one of the potential problems that affects the therapeutic efficacy of MMPs inhibitors. Several MMP inhibitors that show selectivity for various MMPs have been reported in the past few years. This report describes the structural and inhibitory properties of these novel inhibitors, which hold considerable promise for effective targeting of these important enzymes.
基质金属蛋白酶(MMPs)在人类中已发现至少有26种,与多种病理状况有关,包括肿瘤转移、炎症、神经和心血管疾病。抑制MMPs已被广泛视为干预这些疾病进程的一种策略。尽管在过去十年中已开发出大量广谱MMP抑制剂,但这些抑制剂在临床试验中并未达到预期效果。除MMPs外,广谱抑制通常还靶向其他金属蛋白酶,这被认为是影响MMP抑制剂治疗效果的潜在问题之一。在过去几年中已报道了几种对各种MMPs具有选择性的MMP抑制剂。本报告描述了这些新型抑制剂的结构和抑制特性,它们在有效靶向这些重要酶方面具有很大前景。