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A novel selective GABA(A) alpha1 receptor agonist displaying sedative and anxiolytic-like properties in rodents.

机译:一种新型的选择性GABA(A)alpha1受体激动剂在啮齿动物中表现出镇静和抗焦虑的特性。

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摘要

In our pursuit to identify selective ligands for Bz/GABA(A) receptor subtypes, a novel pyrazolo[1,5-a]pyrimidine derivative (4), the azaisostere of zolpidem, was synthesized and evaluated in vitro on bovine brain homogenate and on recombinant benzodiazepine receptors (alphaxbeta2/3gamma2, x = 1-3, 5) expressed in HEK293 cells. Compound 4 displayed affinity only for alpha1beta2gamma2 subtype (K(i) = 31 nM), and in an in-depth, in vivo study it revealed sedative and anxiolytic-like properties without any amnesic and myorelaxant effects in rodents.
机译:为了确定Bz / GABA(A)受体亚型的选择性配体,我们合成了一种新颖的吡唑并[1,5-a]嘧啶衍生物(4),唑吡坦的氮杂异黄酮,并在牛脑匀浆上和体外进行了评估。 HEK293细胞中表达的重组苯并二氮杂pine受体(alphaxbeta2 / 3gamma2,x = 1-3,5)。化合物4仅显示对alpha1beta2gamma2亚型(K(i)= 31 nM)的亲和力,在一项深入的体内研究中,它显示出镇静和抗焦虑的特性,对啮齿类动物没有任何记忆消除和肌肉松弛作用。

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