首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antiproliferative and anti-inflammatory activities of some novel 6-aryl-2-(p-(methanesulfonyl)phenyl)-4,5-dihydropyridazi-3(2H)-ones
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Synthesis, antiproliferative and anti-inflammatory activities of some novel 6-aryl-2-(p-(methanesulfonyl)phenyl)-4,5-dihydropyridazi-3(2H)-ones

机译:一些新型6-芳基-2-(P-(甲磺酰基)苯基)-4,5-二氢吡啶唑-3(2H) - 酮的合成,抗增殖和抗炎活性

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摘要

Sixteen new 6-aryl-2-(p-(methanesulfonyl)phenyl)-4,5-dihydropyridazi-3(2 H)-ones (2a-p) were synthesized and tested for in vitro anticancer and in vivo anti-inflammatory activities. Eleven (2b, 2d , 2-ej and 2m-p) of the obtained compounds were screened for their antiproliferative activity towards 60 human cancer cell lines by the National Cancer Institute (USA). Compound 2f showed remarkable activity with GI50 less than 1 μM on 36 human tumor cell lines and has been referred to Biological Evaluation Committee (NCI) for advance study. Compound 2g also displayed promising antiproliferative activity against 20 different cell lines with GI50 less than 1 μM. Compounds 2k and 2n were found to have a comparable anti-inflammatory activity to that of standard drug etoricoxib in carrageenan-induced rat hind paw edema model at 5 h.
机译:1六个新的6-芳基-2-(p-(甲磺酰基)苯基)-4,5-二氢吡啶唑-3(2小时) - 酮(2A-P)被合成并测试体外抗癌和体内抗炎活性 。 通过国家癌症研究所(美国)筛选所得化合物的110℃(2B,2D,2-EJ和2M-P)的所得化合物的抗增殖活性。 化合物2F在36例人肿瘤细胞系上显示出少于1μm的GI50的显着活性,并已提交预先研究的生物评估委员会(NCI)。 化合物2g还显示出对20种不同细胞系的抗增殖活性,GI50小于1μm。 发现化合物2K和2N在5小时的角叉菜胶诱导的大鼠后爪水肿模型中对标准药物肉毒毒毒剂具有相当的抗炎活性。

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