摘要
为寻找活性更高、降压作用更理想的钾通道开放剂 ,合成了 10个苯并吡喃酯类衍生物及3个中间体 ,并对它们进行了体外低钾诱导的血管收缩抑制试验 .结果表明 :化合物浓度为 1×10 -4 mol/L时对低钾 (2 0mmol/L)引起的血管收缩有不同程度的抑制作用 ,化合物 (Ⅰ )和 (Ⅱa)的活性较好 ,抑制率分别为 86 .4%和 79.3 %
In order to search for new novel antihypertensives,considerable attention was given to the potassium channel openers of benzopyrans.10 esters of benzopyrans were designed and synthesized.The biological activities of the compounds were evaluated.At the dose of 1×10 -4 mol·L -1 ,(Ⅰ) and (Ⅱa) could inhibit the low potassium induced vessel contraction by 86 4% and 79 3% respectively.
出处
《中国药物化学杂志》
CAS
CSCD
2000年第3期157-160,共4页
Chinese Journal of Medicinal Chemistry
基金
国家自然科学基金!No .39370 811
关键词
苯并吡喃酯类衍生物
钾通道开放剂
降压药
合成
esters of benzopyrans
potassium channel openers
synthesis
hypotensive activity