首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Synthesis and biological evaluation of some novel 6-aryl-2-(p- sulfamylphenyl)-4,5-dihydropyridazin-3(2H)-ones as anti-cancer, antimicrobial, and anti-inflammatory agents
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Synthesis and biological evaluation of some novel 6-aryl-2-(p- sulfamylphenyl)-4,5-dihydropyridazin-3(2H)-ones as anti-cancer, antimicrobial, and anti-inflammatory agents

机译:一些新型的6-芳基-2-(对氨基磺酰基苯基)-4,5-二氢哒嗪-3(2H)-酮类化合物的合成及生物学评价,用于抗癌,抗菌和消炎

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摘要

A series of 6-aryl-2-(p-sulfamylphenyl)-4,5-dihydropyridazin-3(2H)-ones (2aj) were synthesized by condensation of the appropriate β-aroylpropionic acid and 4-hydrazinobenzenesulfonamide hydrochloride in ethanol and tested for anti-cancer, anti-inflammatory, and antimicrobial actions. According to the protocol of the National Cancer Institute (NCI) in vitro disease-oriented human cells screening panel assay, compound 2g showed high activity against HL-60 (TB) (leukemia), SR (leukemia), NCI-H522 (non-small-cell lung cancer), and BT-549 (breast cancer) with a GI50 value of less than 2 μM. Two compounds (2c and 2f) were found to have promising anti-inflammatory activity, while a fair number of compounds showed good antifungal activity.
机译:通过将适当的β-芳酰基丙酸和4-肼基苯磺酰胺盐酸盐在乙醇中缩合,合成了一系列6-芳基-2-(对磺酰胺基苯基)-4,5-二氢哒嗪-3(2H)-酮(2aj)。具有抗癌,抗炎和抗菌作用。根据美国国家癌症研究所(NCI)的针对疾病的体外人体细胞筛选小组分析的协议,化合物2g对HL-60(TB)(白血病),SR(白血病),NCI-H522(非GI50值小于2μM的小细胞肺癌)和BT-549(乳腺癌)。发现两种化合物(2c和2f)具有良好的抗炎活性,而相当数量的化合物则具有良好的抗真菌活性。

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