al-Deeb O A, al-Rashood K A, Elkhawad I E, el-Shafie F S, el-Tahir K E
Department of Pharmaceutical Chemistry, and Pharmacology, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Boll Chim Farm. 1997 Dec;136(11):691-5.
A series of 1H-1,4-benzothiazineylides was synthesized and characterized. The influence of this series of compounds 1-7 was examined on the cardiovascular system of the rat, the isolated jejunum of the rabbit, the guinea-pig ileum and the isolated uteri of late pregnant rats. The results of the present study revealed the bradicardiogenic effect of the ethyl, propyl and isobutyl derivatives when tested in the dose range of (10-53 mumole Kg-1). Furthermore, the isobutyl derivative also exhibited an ability to decrease the arterial blood pressure. All the test compounds exhibited non-spasmolytic activity against ACh, histamine and BaCl2. The butyl, isobutyl and isopropyl derivatives were found to be the most potent. The results direct the attention to a new potential group of cardiovascular depressant and spasmolytic agents.
合成并表征了一系列1H-1,4-苯并噻嗪叶立德。考察了该系列化合物1-7对大鼠心血管系统、兔离体空肠、豚鼠回肠和晚期妊娠大鼠离体子宫的影响。本研究结果显示,当在(10-53微摩尔·千克-1)剂量范围内测试时,乙基、丙基和异丁基衍生物具有心动过缓作用。此外,异丁基衍生物还具有降低动脉血压的能力。所有受试化合物对乙酰胆碱、组胺和氯化钡均表现出非解痉活性。发现丁基、异丁基和异丙基衍生物活性最强。这些结果将注意力引向了一类新的潜在心血管抑制剂和解痉剂。