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首页> 外文期刊>Journal of Medicinal Chemistry >8-(4-Methoxyphenyl)pyrazolo[1,5-a]-1,3,5-triazines: Selective and Centrally Active Corticotropin-Releasing Factor Receptor-1 (CRF1) Antagonists
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8-(4-Methoxyphenyl)pyrazolo[1,5-a]-1,3,5-triazines: Selective and Centrally Active Corticotropin-Releasing Factor Receptor-1 (CRF1) Antagonists

机译:8-(4-甲氧基苯基)吡唑并[1,5-a] -1,3,5-三嗪:选择性和中枢活性促肾上腺皮质激素释放因子受体1(CRF1)拮抗剂。

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This report describes the syntheses and structure-activity relationships of 8-(4-methoxyphenyl)pyrazolo[1,5-a]-1,3,5-triazine corticotropin releasing factor receptor-1 (CRF1) receptor antagonists. CRF1 receptor antagonists may be potential anxiolytic or antidepressant drugs. This research culminated in the discovery of analogue 12-3. which is a potent, selective CRF1 antagonist (hCRF(1) IC50 = 4.7 +/- 2.0 nM) with weak affinity for the CRF-binding protein and biogenic amine receptors. This compound also has a good pharmacokinetic profile in dogs. Analogue 12-3 is orally effective in two rat models of anxiety: the defensive withdrawal (situational anxiety) model and the elevated plus maze test. Analogue 12-3 has been advanced to clinical trials.
机译:该报告描述了8-(4-甲氧基苯基)吡唑并[1,5-a] -1,3,5-三嗪促肾上腺皮质激素释放因子受体-1(CRF1)受体拮抗剂的合成与构效关系。 CRF1受体拮抗剂可能是潜在的抗焦虑药或抗抑郁药。这项研究最终发现了类似物12-3。它是一种有效的选择性CRF1拮抗剂(hCRF(1)IC50 = 4.7 +/- 2.0 nM),对CRF结合蛋白和生物胺受体的亲和力较弱。该化合物在狗中也具有良好的药代动力学特征。在两个大鼠焦虑模型中,类似物12-3口服有效:防御性戒断(情境焦虑)模型和高架迷宫测试。类似物12-3已被推进临床试验。

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