Sutradhar Ranajit Kumar, Rahman Akm Matior, Ahmad Mesbahuddin, Bachar Sitesh Chandra, Saha Achinto, Roy Tapashi Ghosh
Department of Chemistry, Chittagong University of Engineering and Technology (CUET), Chittagong-4349, Bangladesh.
Pak J Pharm Sci. 2007 Jul;20(3):185-8.
The analgesic and anti-inflammatory activities of a new alkaloid, 1,2,3,9-tetrahydro-pyrrolo [2,1-b] quinazolin-3-ylamine (compound 1) isolated from Sida cordifolia Linn. were investigated in animal models. In the acetic acid induced writhing model, the compound 1 showed 25.4 (P<0.05) and 52.43% (P<0.01) inhibition of writhing response at doses of 25 and 50 mg/kg body weight respectively. The alkaloid also produced significant increase in the tail flick latency in radiant heat tail-flick method. In Carrageenan induced rat paw edema the compound 1 produced 16.93 and 24.43 % inhibition of paw edema at the doses of 25 and 50 mg/kg body weight respectively at the third hour of study.
对从心叶黄花稔中分离出的一种新生物碱1,2,3,9-四氢-吡咯并[2,1-b]喹唑啉-3-胺(化合物1)的镇痛和抗炎活性进行了动物模型研究。在醋酸诱导的扭体模型中,化合物1在体重剂量分别为25和50mg/kg时,对扭体反应的抑制率分别为25.4%(P<0.05)和52.43%(P<0.01)。该生物碱在辐射热甩尾法中还显著延长了甩尾潜伏期。在角叉菜胶诱导的大鼠足爪水肿模型中,在研究的第三小时,化合物1在体重剂量分别为25和50mg/kg时,对足爪水肿的抑制率分别为16.93%和24.43%。