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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of novel 2-mercapto benzothiazole and 1,2,3-triazole based bis-heterocycles: their anti-inflammatory and anti-nociceptive activities.
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Synthesis of novel 2-mercapto benzothiazole and 1,2,3-triazole based bis-heterocycles: their anti-inflammatory and anti-nociceptive activities.

机译:新型2-巯基苯并噻唑的合成和基于1,2,3-三唑的双杂环:它们的抗炎和抗伤害活性。

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摘要

A focused library of novel bis-heterocycles encompassing 2-mercapto benzothiazole and 1,2,3-triazoles were synthesized using click chemistry approach. The synthesized compounds have been tested for their anti-inflammatory activity by using biochemical cyclooxygenase (COX) activity assays and carrageenan-induced hind paw edema. Among the tested compounds, compound 4d demonstrated a potent selective COX-2 inhibition with COX-2/COX-1 ratio of 0.44. Results from carrageenan-induced hind paw edema showed that compounds 4a, 4d, 4e and 4f posses significant anti-inflammatory activity as compared to the standard drug Ibuprofen. The compounds showing significant activity were further subjected to anti-nociceptive activity by writhing test. These four compounds have shown comparable activity with the standard Ibuprofen. Further ulcerogenic studies shows that none of these compounds causing gastric ulceration.
机译:使用咔哒化学方法合成了包含2-巯基噻唑和1,2,3-三唑的新型双杂环的重点进行了一种聚焦的双杂环库。 已经通过使用生物化学环氧氢止酶(COX)活性测定和角叉菜胶诱导的后爪水肿来测试合成的化合物的抗炎活性。 在测试的化合物中,化合物4D用COX-2 / COX-1的比例显示了有效的选择性COX-2抑制作用0.44。 阿拉胶诱导的后爪水肿的结果表明,与标准药物布洛芬相比,化合物4a,4d,4e和4f具有显着的抗炎活性。 通过卷曲试验,显示出显着活性的化合物进一步进行抗伤害活性。 这四种化合物与标准的布洛芬显示了可比活性。 进一步的溃疡性研究表明,这些化合物都没有引起胃溃疡。

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