氯沙坦
化学
吲哚试验
血管紧张素Ⅱ受体1型
血管紧张素II
体内
药理学
羧酸
化学合成
血管紧张素受体
体外
口服
肾素-血管紧张素系统
放射性配体
受体
血压
立体化学
生物化学
内分泌学
医学
生物技术
生物
作者
Andrey V. Danilenko,Alexander N. Volov,Nikolai A. Volov,Yana B. Platonova,Serguei V. Savilov
标识
DOI:10.1016/j.bmcl.2023.129349
摘要
Molecular design, synthesis, in vitro and in vivo studies of novel derivatives of indole-3-carboxylic acid new series of angiotensin II receptor 1 antagonists is presented. Radioligand binding studies using [125I]-angiotensin II displayed that new derivatives of indole-3-carboxylic acid have a high nanomolar affinity for the angiotensin II receptor (AT1 subtype) on a par with the known pharmaceuticals such as losartan. Biological studies of synthesized compounds in spontaneously hypertensive rats have demonstrated that compounds can lower blood pressure when administered orally. Maximum the decrease in blood pressure was 48 mm Hg with oral administration of 10 mg/kg and antihypertensive effect was observed for 24 h, which is superior to losartan.
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