首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Discovery of NBI-77860/GSK561679, a potent corticotropin-releasing factor (CRF1) receptor antagonist with improved pharmacokinetic properties.
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Discovery of NBI-77860/GSK561679, a potent corticotropin-releasing factor (CRF1) receptor antagonist with improved pharmacokinetic properties.

机译:发现NBI-77860 / GSK561679,一种有效的促肾上腺皮质激素释放因子(CRF1)受体拮抗剂,具有改善的药代动力学特性。

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摘要

Antagonists of the corticotropin-releasing factor (CRF) neuropeptide may prove effective in treating stress and anxiety related disorders. In an effort to identify antagonists with improved physico-chemical properties a new series of CRF(1) antagonists were designed to substitute the propyl groups at the C7 position of the pyrazolo[1,5-a]pyrimidine core of 1 with heterocycles. Compound (S)-8d was identified as a high affinity ligand with a pK(i) value of 8.2 and a functional CRF(1) antagonist with pIC(50) value of 7.0 in the in vitro CRF ACTH production assay.
机译:促肾上腺皮质激素释放因子(CRF)神经肽的拮抗剂可能被证明可有效治疗压力和焦虑症。为了鉴定具有改善的理化性质的拮抗剂,设计了一系列新的CRF(1)拮抗剂,用杂环取代吡唑并[1,5-a]嘧啶核1的C7位置处的丙基。在体外CRF ACTH生产试验中,化合物(S)-8d被鉴定为pK(i)值为8.2的高亲和力配体,而pIC(50)值为7.0的功能性CRF(1)拮抗剂。

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