首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis and characterization of 1,3-dihydro-benzo(b)(1,4)diazepin-2-one derivatives: Part 4. In vivo active potent and selective non-competitive metabotropic glutamate receptor 2/3 antagonists.
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Synthesis and characterization of 1,3-dihydro-benzo(b)(1,4)diazepin-2-one derivatives: Part 4. In vivo active potent and selective non-competitive metabotropic glutamate receptor 2/3 antagonists.

机译:1,3-二氢苯并(b)(1,4)二氮杂-2-酮衍生物的合成和表征:第4部分。体内活性有效和选择性非竞争性代谢型谷氨酸受体2/3拮抗剂。

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摘要

This study completes a series of papers devoted to the characterization of the non-competitive mGluR2/3 antagonist properties of 1,3-dihydro-benzo[b][1,4]diazepin-2-one derivatives with particular emphasis on derivatizations compatible with brain penetration and in vivo activity. Especially the compounds bearing a para-pyridine consistently showed in vivo activity in rat behavioral models after oral administration, for example, blockade of the mGluR2/3 agonist LY354740-induced hypoactivity and improvement of a working memory deficit induced either by LY354740 or scopolamine in the delayed match to position task (DMTP). Moreover, combination studies with a cholinesterase inhibitor show apparent synergistic effects on working memory impairment induced by scopolamine.
机译:这项研究完成了一系列致力于1,3-二氢-苯并[b] [1,4]二氮杂-2--2-酮衍生物的非竞争性mGluR2 / 3拮抗剂特性表征的论文,特别着重于与脑部渗透和体内活性。特别是带有对吡啶的化合物在口服后在大鼠行为模型中始终表现出体内活性,例如,mGluR2 / 3激动剂LY354740诱导的机能减退被阻断,以及LY354740或东pol碱引起的工作记忆障碍的改善。延迟匹配定位任务(DMTP)。此外,与胆碱酯酶抑制剂的联合研究表明,对东pol碱引起的工作记忆障碍有明显的协同作用。

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