止痛药
解热药
药理学
萜类
二萜
鼠尾草
毒性
急性毒性
卡拉胶
化学
医学
水肿
生药学
传统医学
生物活性
立体化学
体外
生物化学
外科
内科学
作者
M. Hernández‐Pérez,Rosa M. Rabanal,M. C. DE LA TORRE,Blanca Rodríguez
出处
期刊:Planta Medica
[Georg Thieme Verlag KG]
日期:1995-12-01
卷期号:61 (06): 505-509
被引量:90
标识
DOI:10.1055/s-2006-959358
摘要
Aethiopinone (1), an o-naphthoquinone diterpene from Salvia aethiopis L. roots and two hemisynthetic derivatives 2 and 3 have been evaluated for toxicity, anti-inflammatory, analgesic, antipyretic, and haemostatic activities. The compounds tested showed low toxicity and a pharmacological profile similar to other NSAI substances on reducing the edema induced by carrageenan and contractions induced by phenyl-p-quinone; the most active compounds were 1 and 2. In the same way and as expected with these types of substances, the bleeding time increased. In the TPA-induced ear inflammation model, the three compounds showed a moderate reduction of edema, and 1 produced a significant increase in the reaction time against thermal painful stimuli in the tail immersion test. The results demonstrated strong anti-inflammatory, peripheral and central analgesic properties for 1, as well as antiedematose topical action and peripheral analgesic properties for 2 and 3.
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