The potential for caspases in drug discovery.

Sarah H MacKenzie, Joshua L Schipper, A Clay Clark
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Abstract

Caspases are a family of proteases that are involved in the execution of apoptosis and the inflammatory response. A plethora of diseases occur as a result of the dysregulation of apoptosis and inflammation, and caspases have been targeted as a therapeutic strategy to halt the progression of such diseases. Hundreds of peptide and peptidomimetic inhibitors have been designed and tested, but only a few have advanced to clinical trials because of poor drug-like properties and pharmacological constraints. Although much effort has been focused on inhibiting caspases, there are many diseases that result from a decrease in apoptosis, thus activating procaspases could also be a viable therapeutic strategy. To this end, recent efforts have focused on the design of procaspase-3 activators. This review highlights the current progress in the rational design of both specific and pan-caspase inhibitors, as well as procaspase-3 activators.

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半胱天冬酶在药物发现中的潜力。
半胱天冬酶是一组参与细胞凋亡和炎症反应的蛋白酶。大量的疾病是由于细胞凋亡和炎症的失调而发生的,半胱天冬酶已经被作为一种治疗策略来阻止这些疾病的进展。已经设计和测试了数百种肽和拟肽抑制剂,但由于药物性质差和药理学限制,只有少数进入临床试验。尽管抑制半胱天冬酶的研究有很多,但许多疾病是由细胞凋亡减少引起的,因此激活半胱天冬酶也可能是一种可行的治疗策略。为此,最近的努力集中在procaspase-3激活剂的设计上。本文综述了目前在合理设计特异性和泛caspase抑制剂以及procaspase-3激活剂方面的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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