Novelli Federica, Sparatore Fabio
Dipartimento di Scienze Farmaceutiche, University of Genoa, Viale Benedetto XV, 3, 16132 Genova, Italy.
Farmaco. 2002 Nov;57(11):871-82. doi: 10.1016/s0014-827x(02)01293-4.
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.
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。