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首页> 外文期刊>International Journal of Pharmaceutical Sciences Review and Research >CHEWING GUM: A FRIENDLY ORAL MUCOSAL DRUG DELIVERY SYSTEMby Anand S. Surana, India. 013 REMEDIAL APPROACH: SWINE FLUby Pankaj Pradhan, Neha Kaushik, Pankaj Bhateja, Abhimanyu, India. 014 EVALUATION OF HEPATOPROTECTIVE ACTIVITY OF GLYCOSMIS PENTAPHYLLA ROOTS AGAINST CCl4 – INDUCED ACUTE LIVER INJURY IN RATSby N. Jaya raju*, B. Ganga rao, India. 015 FAST DISSOLVING TABLETS: PREPARATION, CHARACTERIZATION AND EVALUATION: AN OVERVIEW
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CHEWING GUM: A FRIENDLY ORAL MUCOSAL DRUG DELIVERY SYSTEMby Anand S. Surana, India. 013 REMEDIAL APPROACH: SWINE FLUby Pankaj Pradhan, Neha Kaushik, Pankaj Bhateja, Abhimanyu, India. 014 EVALUATION OF HEPATOPROTECTIVE ACTIVITY OF GLYCOSMIS PENTAPHYLLA ROOTS AGAINST CCl4 – INDUCED ACUTE LIVER INJURY IN RATSby N. Jaya raju*, B. Ganga rao, India. 015 FAST DISSOLVING TABLETS: PREPARATION, CHARACTERIZATION AND EVALUATION: AN OVERVIEW

机译:口香糖:一种友好的口腔粘膜药物输送系统,印度Anand S. Surana着。 013补救措施:猪流感印度印度阿比曼尤邦Pankaj Bhateja的Pankaj Pradhan,Neha Kaushik提供。 014对印度五加糖对大鼠CCl4诱发的急性肝损伤的预防作用N. Jaya raju *,B。Ganga rao,印度。 015快速溶解片剂:制备,鉴定和评估:概述

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A series of new 3-formyl coumarine (2) was synthesized in good yields by replacement of chlorine atom by 2nd amines. In addition, 5-chromeno-pyrido[2,3-d]pyrimidine-4-yl derivatives (5,6) was synthesized by cyclocondensation of 6- aminouracil, the respective ketones and 3-formyl coumarine (2) in one pot-synthesis. Also 2-S-nucleosides analogous of pyrido[2,3-d]-pyrimidines (12-15) was synthesized by a simple method in good yields, The new compounds were evaluated for their anti-inflammatory and analgesic activity. It has been found that the derivatives 5a, 5b, 14a, 14b, 15a and 15c exhibited the dual pharmacological activities with superior gastrointestinal safety profile when compared to indomethacin except 5a which resulted in ulcer lesions in many of the experimental rats.
机译:通过用第二种胺取代氯原子,以高收率合成了一系列新的3-甲酰基香豆碱(2)。另外,通过6-氨基尿嘧啶,相应的酮和3-甲酰基香豆碱(2)在一个锅中的环缩合反应,合成了5-chromeno-pyrido [2,3-d] pyrimidine-4-yl衍生物(5,6)。合成。还通过简单方法以高收率合成了类似吡啶并[2,3-d]-嘧啶(12-15)的2-S-核苷。评估了这些新化合物的抗炎和镇痛活性。已经发现,与吲哚美辛相比,衍生物5a,5b,14a,14b,15a和15c具有双重胃肠道药理活性,具有优异的胃肠道安全性,除了5a会导致许多实验大鼠的溃疡损伤。

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