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新型哒嗪酮衍生物用于合成具有环氧化酶抑制活性的强效镇痛和抗炎化合物的研究。

Investigations of new pyridazinone derivatives for the synthesis of potent analgesic and anti-inflammatory compounds with cyclooxygenase inhibitory activity.

作者信息

Okçelik Berna, Unlü Serdar, Banoglu Erden, Küpeli Esra, Yeşilada Erdem, Sahin M Fethi

机构信息

Division of Pharmaceutical Sciences, Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Gazi University, 6330 Etiler, Ankara, Turkey.

出版信息

Arch Pharm (Weinheim). 2003 Sep;336(9):406-12. doi: 10.1002/ardp.200300778.

DOI:10.1002/ardp.200300778
PMID:14528488
Abstract

In this study we describe the synthesis of two novel 4-phenyl-and 4-(2-chlorophenyl)-6-(5-chloro-2-oxo-3H-benzoxazol-7-yl)-3(2H)-pyridazinone derivatives (compounds 8a and b) and their testing as inhibitors of cyclooxygenases (COX-1 and COX-2). Both compounds inhibited COX-1 (by 59 % and 61 % for compounds 8a and 8b respectively and COX-2 (by 37 % and 28 % for compounds 8a and 8b respectively) at a concentration of 10 microM. Furthermore, we tested the analgesic and anti-inflammatory activities of the synthesized compounds in vivo by using the p-benzoquinone-induced writhing test and the carrageenan-induced hind paw edema model, respectively. Compounds 8a and 8b showed potent analgesic and anti-inflammatory activities without causing gastric lesions in the tested animals.

摘要

在本研究中,我们描述了两种新型4-苯基和4-(2-氯苯基)-6-(5-氯-2-氧代-3H-苯并恶唑-7-基)-3(2H)-哒嗪酮衍生物(化合物8a和8b)的合成及其作为环氧化酶(COX-1和COX-2)抑制剂的测试。在浓度为10微摩尔时,两种化合物均抑制COX-1(化合物8a和8b分别为59%和61%)以及COX-2(化合物8a和8b分别为37%和28%)。此外,我们分别使用对苯醌诱导的扭体试验和角叉菜胶诱导的后爪水肿模型,在体内测试了合成化合物的镇痛和抗炎活性。化合物8a和8b显示出强效的镇痛和抗炎活性,且在受试动物中未引起胃部损伤。

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