importance. Herein we report the development of a series of tetrahydroindazole compounds that are highly potent and selective for sigma‐2. Structure–activity relationship data were used to generate a pharmacophore model that summarizes the common features present in the potent ligands. Assays for solubility and microsomal stability showed that several members of this compound series possess promising characteristics
业已证明sigma-2受体在许多重要疾病(包括中枢神经系统(CNS)疾病和癌症)中起着重要作用。但是,尚不清楚sigma-2促成这些疾病的机制。因此,开发新的sigma-2
配体非常重要,该
配体可用于探测这种蛋白质的功能,并有可能作为药物开发的先导。在本文中,我们报告了一系列对sigma-2具有高度效力和选择性的四氢
吲唑化合物的开发。结构-活性关系数据被用于生成药效基团模型,该模型总结了有效
配体中存在的共同特征。