止痛药
化学
醋酸
单萜
急性毒性
热板试验
生物活性
热板
药理学
立体化学
毒性
有机化学
生物化学
受体
体外
医学
材料科学
复合材料
伤害
作者
Konstantin Ponomarev,Е. А. Морозова,А. В. Павлова,Е. В. Суслов,Д. В. Корчагина,Andrey A. Nefedov,Т. Г. Толстикова,К. П. Волчо,N. F. Salakhutdinov
出处
期刊:Medicinal Chemistry
[Bentham Science Publishers]
日期:2017-11-08
卷期号:13 (8)
被引量:8
标识
DOI:10.2174/1573406413666170525124316
摘要
It was found earlier that compounds combining diazaadamantane and monoterpene moieties possessed promising analgesic activity along with low acute toxicity and the lack of ulcerogenic activity.In this paper, new structural analogues of the most active compounds were synthesized and evaluated for their analgesic activity.Their structures were confirmed by various analytical methods, such as 1H and 13C NMR, HRMS. All of them were evaluated for analgesic activity at a dose of 20 mg/kg or less using acetic acid-induced writhing test and hot plate test.Some compounds showed analgesic activity in acetic acid-induced writhing test. One of the synthesized compounds demonstrated high analgesic activity in both tests with 46% effect in acetic acid-induced writhing test and 89% effect in hot plate test. Both structural fragments of this compound did not possess any analgesic effect at a dose of 20 mg/kg.Structure-activity relationships indicated that the most active compound combines fragments of (-)-myrtenal and 6-amino-5,7-dimethyl-1,3-diazaadamantane. Both parts of the molecule are important for demonstrating analgesic activity.
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