Timmermans P B, Carini D J, Chiu A T, Duncia J V, Price W A, Wells G J, Wong P C, Wexler R R, Johnson A L
E.I. du Pont de Nemours & Company, Medical Products Department, Wilmington, Del.
Blood Vessels. 1990;27(2-5):295-300. doi: 10.1159/000158821.
The most direct approach to block the function of the renin-angiotensin system would be to antagonize angiotensin II (AII) at the level of its receptor. However, the AII receptor antagonists currently available, such as saralasin, are peptides which still retain agonistic activity and lack oral bioavailability. We have identified the N-benzylimidazoles, S-8307 and S-8308, as weak, but selective nonpeptide AII receptor antagonists. These initial leads were subsequently converted into more potent compounds, such as EXP6155, EXP6803 and EXP7711, while maintaining the selectivity. The compounds displace 3H-AII from its specific binding sites in adrenal cortical membranes and smooth muscle cells. They competitively inhibit the vasoconstrictor response to AII in various in vivo and in vitro preparations, but do not influence those to KCl, norepinephrine, and vasopressin. Converting enzyme and renin are not affected by these agents. In renal hypertensive rats and sodium-depleted dogs our compounds cause a sustained decrease in arterial pressure following intravenous and oral (EXP7711) administration, and are devoid of agonistic properties. Taken together, these nonpeptide structures are true competitive AII receptor antagonists and represent a new class of effective antihypertensive agents.
阻断肾素-血管紧张素系统功能的最直接方法是在其受体水平拮抗血管紧张素II(AII)。然而,目前可用的AII受体拮抗剂,如沙拉新,是仍保留激动活性且缺乏口服生物利用度的肽类。我们已确定N-苄基咪唑类化合物S-8307和S-8308为弱的但具有选择性的非肽类AII受体拮抗剂。这些最初的先导化合物随后被转化为更有效的化合物,如EXP6155、EXP6803和EXP7711,同时保持选择性。这些化合物可从肾上腺皮质膜和平滑肌细胞中的特异性结合位点置换3H-AII。它们在各种体内和体外实验制剂中竞争性抑制对AII的血管收缩反应,但不影响对氯化钾、去甲肾上腺素和血管加压素的反应。转化酶和肾素不受这些药物影响。在肾性高血压大鼠和失钠犬中,我们的化合物静脉注射和口服(EXP7711)后可使动脉压持续降低,且无激动特性。综上所述,这些非肽结构是真正的竞争性AII受体拮抗剂,代表了一类新型有效的抗高血压药物。