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5-HT1A 受体药效团筛选用于筛选 α1-肾上腺素能受体拮抗剂的非靶标活性。

5-HT1A receptor pharmacophores to screen for off-target activity of α1-adrenoceptor antagonists.

机构信息

Department of Pharmacology, School of Medical Sciences, The University of New South Wales, UNSW Sydney, NSW, 2052, Australia.

出版信息

J Comput Aided Mol Des. 2013 Apr;27(4):305-19. doi: 10.1007/s10822-013-9647-5. Epub 2013 Apr 27.

Abstract

The α1-adrenoceptors (α1-ARs), in particular the α1A-AR subtype, are current therapeutic targets of choice for the treatment of urogenital conditions, such as benign prostatic hyperplasia (BPH). Due to the similarity between the transmembrane domains of the α1-AR subtypes, and the serotonin receptor subtype 1A (5-HT1A-R), currently used α1-AR subtype-selective drugs to treat BPH display considerable off-target affinity for the 5-HT1A-R, leading to side effects. We describe the construction and validation of pharmacophores for 5-HT1A-R agonists and antagonists. Through the structural diversity of the training sets used in their development, these pharmacophores define the properties of a compound needed to bind to 5-HT1A receptors. Using these and previously published pharmacophores in virtual screening and profiling, we have identified unique chemical compounds (hits) that fit the requirements to bind to our target, the α1A-AR, selectively over the off-target, the 5-HT1A-R. Selected hits have been obtained and their affinities for α1A-AR, α1B-AR and 5-HT1A-R determined in radioligand binding assays, using membrane preparations which contain human receptors expressed individually. Three of the tested hits demonstrate statistically significant selectivity for α1A-AR over 5-HT1A-R. All seven tested hits bind to α1A-AR, with two compounds displaying K i values below 1 μM, and a further two K i values of around 10 μM. The insights and knowledge gained through the development of the new 5-HT1A-R pharmacophores will greatly aid in the design and synthesis of derivatives of our lead compound, and allow the generation of more efficacious and selective ligands.

摘要

α1-肾上腺素受体(α1-ARs),特别是 α1A-AR 亚型,是治疗泌尿生殖系统疾病(如良性前列腺增生症,BPH)的当前首选治疗靶点。由于 α1-AR 亚型和 5-羟色胺受体亚型 1A(5-HT1A-R)的跨膜结构域相似,目前用于治疗 BPH 的 α1-AR 亚型选择性药物对 5-HT1A-R 具有相当大的非靶点亲和力,导致副作用。我们描述了 5-HT1A-R 激动剂和拮抗剂的药效团构建和验证。通过在其开发过程中使用的训练集的结构多样性,这些药效团定义了与 5-HT1A 受体结合所需的化合物的性质。通过使用这些和以前发表的药效团进行虚拟筛选和分析,我们已经确定了独特的化学化合物(命中物),它们符合结合我们的靶标,即 α1A-AR,而不是非靶标,5-HT1A-R 的要求。已获得选定的命中物,并使用包含单独表达的人受体的膜制剂在放射性配体结合测定中确定了它们对 α1A-AR、α1B-AR 和 5-HT1A-R 的亲和力。测试的三个命中物显示出对 α1A-AR 的统计学上显著选择性,超过 5-HT1A-R。所有七种测试的命中物都与 α1A-AR 结合,两种化合物的 K i 值低于 1 μM,另外两种化合物的 K i 值约为 10 μM。通过开发新的 5-HT1A-R 药效团获得的见解和知识将极大地有助于我们的先导化合物的设计和合成,并允许生成更有效和选择性的配体。

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