Synthesis and Pharmacological Activity of a New Series of 1-(1<i>H</i>-Indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol Analogs
作者:Marek Bednarski、Monika Otto、Magdalena Dudek、Marcin Kołaczkowski、Adam Bucki、Agata Siwek、Grażyna Groszek、Elżbieta Maziarz、Piotr Wilk、Jacek Sapa
DOI:10.1002/ardp.201500234
日期:2016.3
different mechanisms, such as nitric oxide (NO) release, β2‐agonistic action, α1‐blockade, antioxidant action, and Ca2+ entry blockade. Here, a study on evaluation of the cardiovascular activity of five new compounds is presented. Compound 3a is a methyl and four of the tested compounds (3b–e) are dimethoxy derivatives of 1‐(1H‐indol‐4‐yloxy)‐3‐(2‐(2‐methoxyphenoxy)ethylamino)propan‐2‐ol. The obtained results
β-肾上腺素能受体拮抗剂是治疗心血管疾病的重要疗法。在β-受体阻滞剂组中,除抑制β-肾上腺素能受体外,还具有重要辅助特性的第三代药物备受关注。这些药物的血管舒张活性是通过不同的机制产生的,例如一氧化氮 (NO) 释放、β2 激动作用、α1 阻断、抗氧化作用和 Ca2+ 进入阻断。在这里,介绍了对五种新化合物的心血管活性评估的研究。化合物 3a 是甲基,四个测试化合物 (3b-e) 是 1-(1H-indol-4-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol 的二甲氧基衍生物。