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沉默调节蛋白抑制剂:亲和力与选择性的研究方法

Sirtuins inhibitors: the approach to affinity and selectivity.

作者信息

Cen Yana

机构信息

Department of Pharmacology, Weill Medical College of Cornell University, New York, NY 10065, USA.

出版信息

Biochim Biophys Acta. 2010 Aug;1804(8):1635-44. doi: 10.1016/j.bbapap.2009.11.010. Epub 2009 Nov 18.

Abstract

Accumulating evidence has indicated the importance of sirtuins (class III histone deacetylases) in various biological processes. Their potential roles in metabolic and neurodegenerative diseases have encouraged scientists to seek potent and selective sirtuin inhibitors to investigate their biological functions with a view to eventual new therapeutic treatments. This article surveys current knowledge of sirtuin inhibitors including those discovered via high-throughput screening (HST) or via mechanism-based drug design from synthetic or natural sources. Their inhibitory affinity, selectivities, and possible inhibition mechanisms are discussed.

摘要

越来越多的证据表明,沉默调节蛋白(Ⅲ类组蛋白去乙酰化酶)在各种生物过程中具有重要作用。它们在代谢性疾病和神经退行性疾病中的潜在作用促使科学家寻找强效且具有选择性的沉默调节蛋白抑制剂,以研究其生物学功能,最终实现新的治疗方法。本文综述了目前关于沉默调节蛋白抑制剂的知识,包括那些通过高通量筛选(HST)或基于机制的药物设计从合成或天然来源发现的抑制剂。讨论了它们的抑制亲和力、选择性和可能的抑制机制。

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