Guérémy C, Audiau F, Renault C, Benavides J, Uzan A, Le Fur G
J Med Chem. 1986 Aug;29(8):1394-8. doi: 10.1021/jm00158a013.
A series of 4-amino-6-chloro-2-piperazinopyrimidines were synthesized and evaluated for their ability to interact with alpha 1- and alpha 2-adrenoceptors in vitro in binding assays using [3H]WB-4101, [3H]clonidine, and [3H]idazoxan as radioligands. Some compounds were also tested as inhibitors of [3H]spiroperidol binding. Several members of this series showed high and selective affinity for alpha 2-adrenoceptors. The nature of the 4-amino substituent seems to be the most critical factor in determining the potency at these receptors.
合成了一系列4-氨基-6-氯-2-哌嗪基嘧啶,并在体外结合试验中使用[3H]WB-4101、[3H]可乐定和[3H]咪唑克生作为放射性配体,评估它们与α1和α2肾上腺素能受体相互作用的能力。一些化合物还作为[3H]螺哌啶醇结合的抑制剂进行了测试。该系列中的几个成员对α2肾上腺素能受体表现出高亲和力和选择性。4-氨基取代基的性质似乎是决定这些受体活性的最关键因素。