苯并咪唑及其衍生物抗高血压药物的合成、表征及生物学评价

Silky Sethy, S. Mandal, E. Ewies, Neerupma Dhiman, A. Garg
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引用次数: 1

摘要

本文合成了一种取代苯并咪唑和苯并咪唑衍生物,通过拮抗血管紧张素II (Ang II)受体而具有降压活性。用急性肾性高血压模型研究了化合物的体内降压活性。两种化合物TG 1和TG 3被发现具有与替米沙坦相当的降压活性,替米沙坦是血管紧张素II受体拮抗剂类药物的原型。在一项降压研究中,化合物TG 1、TG 2和TG 3的收缩压分别为147.2 mm/Hg、168.2 mm/Hg和126.3 mm/Hg。这一收缩压低于疾病对照组,后者的收缩压为167.2 mm/Hg。实验组舒张压分别为119.7 mm/Hg、124.7 mm/Hg和88.83 mm/Hg,对照组舒张压为122.3 mm/Hg。与替米沙坦相比,TG 3在MABP上有相当的下降。这些令人鼓舞的结果使复方甘油三酯成为有效的抗高血压候选药物,值得进一步研究。
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Synthesis, Characterization and Biological Evaluation of Benzimidazole and Benzindazole Derivatives as Anti-hypertensive Agents
A substituted benzimidazole and benzindazole derivatives had been synthesized having antihypertensive activity through antagonizing the angiotensin II (Ang II) receptors. The in vivo antihypertensive activity of the compounds was done with acute renal hypertension model. Two compounds TG 1 and TG 3 were found to have antihypertensive activity comparable to Telmisartan which is a prototype for Angiotensin II receptor antagonists class of drugs.In an antihypertensive study the compounds TG 1, TG 2 and TG 3 had systolic blood pressures of 147.2 mm/Hg, 168.2 mm/Hg, and 126.3 mm/Hg, respectively. This systolic blood pressure was lower than the disease control vehicle-treated rodents, which had a systolic blood pressure of 167.2 mm/Hg. The diastolic blood pressure was 119.7 mm/Hg, 124.7 mm/Hg and 88.83 mm/Hg, respectively and that of the disease control vehicle-treated rodents was 122.3 mm/Hg. TG 3 had comparable decrease in the MABP to Telmisartan. These encouraging results make compound TG 3 effective anti-hypertensive drug candidate and worthy of further investigation.
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