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Antagonism/Agonism modulation to build novel antihypertensives selectively triggering i1-imidazoline receptor activation

机译:拮抗/激动调节作用,以构建选择性触发i1-咪唑啉受体激活的新型降压药

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摘要

Pharmacological studies have suggested that I1-imidazoline receptors are involved in the regulation of cardiovascular function and that selective I1-agonists, devoid of the side effects associated with the common hypotensive α2-adrenoreceptor agonists, might be considered as a second generation of centrally acting antihypertensives. Therefore, in the present study, inspired by the antihypertensive behavior of our selective I1-agonist 4, we designed, prepared, and studied the novel analogues 5-9. A selective I1-profile, associated with significant hemodinamic effects, was displayed by 5, 8, and 9. Interestingly, the highest potency and longest lasting activity displayed by 8 (carbomethyline) suggested that van der Waals interactions, promoted by the ortho methyl decoration of its aromatic moiety, are particularly advantageous. In addition, in analogy to what was noted for (S)-(+)-4, the observation that only (S)-(+)-8 displayed significant hemodynamic effects unequivocally confirmed the stereospecific nature of the I1 proteins.
机译:药理学研究表明,I1-咪唑啉受体参与心血管功能的调节,而没有常见的降压α2-肾上腺素受体激动剂相关副作用的选择性I1-激动剂可被视为第二代中枢性降压药。因此,在本研究中,受选择性I1-激动剂4的抗高血压行为的启发,我们设计,制备和研究了新型类似物5-9。 5、8和9显示了选择性的I1谱,与显着的血液动力学作用有关。有趣的是,8(羧甲氨酸)显示的最高效能和最长的持久活性表明,邻甲基修饰可促进范德华相互作用其芳族部分的“α”是特别有利的。此外,类似于(S)-(+)-4的发现,只有(S)-(+)-8显示出显着的血液动力学作用的观察明确地证实了I1蛋白的立体特异性。

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