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烷基硫基-1,2,4-三唑,一种新型别构缬氨酸含有蛋白抑制剂。合成与构效关系。

Alkylsulfanyl-1,2,4-triazoles, a new class of allosteric valosine containing protein inhibitors. Synthesis and structure-activity relationships.

机构信息

Nerviano Medical Sciences S.r.l., Oncology, Viale Pasteur 10, 20014 Nerviano (MI), Italy.

出版信息

J Med Chem. 2013 Jan 24;56(2):437-50. doi: 10.1021/jm3013213. Epub 2013 Jan 4.

Abstract

Valosine containing protein (VCP), also known as p97, is a member of AAA ATPase family that is involved in several biological processes and plays a central role in the ubiquitin-mediated degradation of misfolded proteins. VCP is an ubiquitously expressed, highly abundant protein and has been found overexpressed in many tumor types, sometimes associated with poor prognosis. In this respect, VCP has recently received a great deal of attention as a potential new target for cancer therapy. In this paper, the discovery and structure-activity relationships of alkylsulfanyl-1,2,4-triazoles, a new class of potent, allosteric VCP inhibitors, are described. Medicinal chemistry manipulation of compound 1, identified via HTS, led to the discovery of potent and selective inhibitors with submicromolar activity in cells and clear mechanism of action at consistent doses. This represents a first step toward a new class of potential anticancer agents.

摘要

包含缬氨酸的蛋白(VCP),也被称为 p97,是 AAA ATP 酶家族的一员,参与多种生物学过程,并在泛素介导的错误折叠蛋白降解中发挥核心作用。VCP 是一种广泛表达的、高度丰富的蛋白质,在许多肿瘤类型中发现过度表达,有时与预后不良有关。在这方面,VCP 最近作为癌症治疗的潜在新靶点受到了极大的关注。本文描述了烷基硫基-1,2,4-三唑的发现和构效关系,这是一类新的强效、变构的 VCP 抑制剂。通过高通量筛选(HTS)鉴定的化合物 1 的药物化学修饰导致发现了具有亚微摩尔细胞活性的强效和选择性抑制剂,并在一致剂量下具有明确的作用机制。这代表着向一类新的潜在抗癌药物迈出了第一步。

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