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Synthesis and pharmacological activity of pyrazolopyrrolopyrimidine derivatives having vasorelaxing activity.

机译:具有血管松弛活性的吡唑并吡咯并嘧啶衍生物的合成和药理活性。

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摘要

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.
机译:合成了一系列新的5-取代和5-未取代的吡唑并吡咯并嘧啶衍生物,并评估了它们的血管舒张作用和降压活性。如方案I-III所示,通过使用三种关键中间体(7、16和24)有效地完成了合成。根据大鼠主动脉的血管舒张活性(体外)和大鼠的降压活性(体内),确定了所需的药理活性。具体而言,化合物25表现出最强的活性,并且似乎是开发新的抗高血压药的有希望的临床先导。

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