具有血管舒张活性的吡唑吡喃嘧啶衍生物的合成及药理活性。

Drug design and discovery Pub Date : 1999-08-01
T Kumagai, H Matsunaga, S Kaneda, H Shimizu, E Ebisawa, M Kitamura, T Suzuki, M Yuasa, Y Nagao
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引用次数: 0

摘要

合成了一系列新的5-取代和5-非取代吡唑吡喃嘧啶衍生物,并对其血管舒张和降压活性进行了评价。通过使用三个关键中间体(7,16和24),如方案I-III所示,有效地完成了合成。通过对大鼠主动脉的血管舒张活性(体外)和对大鼠的降血压活性(体内)来确定预期的药理活性。具体而言,化合物25表现出最强的活性,似乎是一种新的抗高血压药物开发的有希望的临床先导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and pharmacological activity of pyrazolopyrrolopyrimidine derivatives having vasorelaxing activity.

A new series of 5-substituted and 5-nonsubstituted pyrazolopyrrolopyrimidine derivatives were synthesized, and their vasorelaxing and hypotensive activities were evaluated. The syntheses were efficiently accomplished through the use of three key intermediates (7, 16, and 24), as shown in Schemes I-III. The desired pharmacological activities were confirmed on the basis of vasorelaxing activity in rat aorta (in vitro) and hypotensive activity in rats (in vivo). Specifically, compound 25 exhibited the strongest activity and appears to be a promising clinical lead for the development of a new antihypertensive agent.

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