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螺[1,2,4-苯并三嗪-3(4H),4'-(1'-取代)哌啶]及相关化合物作为σ受体的配体。

Spiro[1,2,4-benzotriazine-3(4H),4'-(1'-substituted)piperidines] and related compounds as ligands for sigma receptors.

作者信息

Novelli Federica, Sparatore Fabio

机构信息

Dipartimento di Scienze Farmaceutiche, University of Genoa, Viale Benedetto XV, 3, 16132 Genova, Italy.

出版信息

Farmaco. 2002 Nov;57(11):871-82. doi: 10.1016/s0014-827x(02)01293-4.

Abstract

As analogues of some conformationally restricted spiropiperidine derivatives which are endowed with high affinity for sigma1 receptor, a set of 16 spiro[1,2,4-benzotriazine-3(4H),4'-(1'-substituted)piperidines] and congeneric compounds was prepared and tested for affinity to sigma1 receptor subtype. All N-arylalkyl substituted derivatives exhibited high affinity for the relevant receptor, with Ki in the low nanomolar range. Affinity for sigma2 subtype (assayed only for a few representative compounds) was from one to three order of magnitude lower. Spiro[1,2,4-benzotriazine-3(4H),4'-(1'-benzyl)piperidine] (2), with a ratio Ki sigma2/Ki sigma1 = 7000 should represent the most selective sigma1 ligand so far described.

摘要

作为一些对σ1受体具有高亲和力的构象受限螺哌啶衍生物的类似物,制备了一组16种螺[1,2,4-苯并三嗪-3(4H),4'-(1'-取代)哌啶]及其同类化合物,并测试了它们对σ1受体亚型的亲和力。所有N-芳基烷基取代衍生物对相关受体均表现出高亲和力,其抑制常数(Ki)处于低纳摩尔范围。对σ2亚型的亲和力(仅对少数代表性化合物进行了测定)低一至三个数量级。螺[1,2,4-苯并三嗪-3(4H),4'-(1'-苄基)哌啶](2),其Kiσ2/Kiσ1比值为7000,应是迄今为止所描述的最具选择性的σ1配体。

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