首页> 外文期刊>Pharmaceutical Chemistry Journal >Synthesis, Affinity for Central Benzodiazepine Receptors, and Hypnosedative and Anxiolytic Properties of 3-Acyloxy-5-Aryl-7-Bromo-1,2-Dihydro-3H-1,4-Benzodiazepin-2-Ones
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Synthesis, Affinity for Central Benzodiazepine Receptors, and Hypnosedative and Anxiolytic Properties of 3-Acyloxy-5-Aryl-7-Bromo-1,2-Dihydro-3H-1,4-Benzodiazepin-2-Ones

机译:合成,对中枢苯二氮卓受体的亲和力,以及3-酰氧基-5-芳基-7-溴-1,2-二氢-3H-1,4-苯并二氮嘧啶-2-β-1,4-苯并二氮素-2-抑制性和抗焦力性质

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摘要

3-Acyloxy-5-aryl-7-bromo-1,2-dihydro-3H-1,4-benzodiazepin-2-ones (3 - 18) were synthesized and shown to possess (ED50 = 0.05 - 5 mg/kg) hypnotic, sedative, anticonvulsant, and anxiolytic properties. The hypnotic activity of the tested compounds varied in the dose range 0.22 - 1.50 mg/kg i.p. in mice. The pharmacological properties of 3 - 14 were comparable to those of cinazepam (Levana((R)) IC) and its metabolite 3-hydroxyphenazepam. The CBDR affinity was shown to increase with acyl length in the series C2-C5 whereas it decreased significantly in the series C6-C8. The tested compounds were characterized by low toxicity with LD50 > 650 mg/kg i.p. in mice.
机译:合成3-酰氧基-5-芳基-7-溴-1,2-二氢-3H-1,4-苯并二氮杂-2- 1,4-苯并二氮素-2-α-1,4-苯并二氮素-2-β-1,4-苯并二氮藻(3-18),所示(ED50 = 0.05-5 mg / kg) 催眠,镇静剂,抗惊厥和抗焦虑性。 测试化合物的催眠活性在剂量范围内变化0.22-1.50mg / kg I.P。 在老鼠中。 3-14的药理学特性与Cazazepam(Levana(r))IC)及其代谢物3-羟基血红素泮相当。 显示CBDR亲和力在C2-C5系列中的酰基长度增加,而C6-C8系列中显着降低。 测试化合物的特征在于LD50> 650mg / kg I.P的低毒性。 在老鼠中。

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