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Preparation and biological evaluation of 6/7-trifluoromethyl(nitro)-, 6,7-difluoro-3-alkyl (aryl)-substituted-quinoxalin-2-ones. Part 3.
Il Farmaco Pub Date : 1999-06-17 , DOI: 10.1016/s0014-827x(99)00011-7
P Sanna , A Carta , M Loriga , S Zanetti , L Sechi

A new series of quinoxalinones 6/7-trifluoromethyl or nitro- and 6,7-difluoro substituted bearing various side-chains (alkyl, halogenoalkyl, benzyl and phenyl groups) at C-3 of the ring system was synthesized and submitted to preliminary in vitro evaluation for antibacterial, antifungal, antimycobacterial, anticancer and anti-HIV activities. Results of these screenings showed that compounds 23-28 exhibited a good inhibition activity against various strains of Candida. Compound 24 showed also an interesting in vitro anticancer activity.

中文翻译:

6 / 7-三氟甲基(硝基)-,6,7-二氟-3-烷基(芳基)取代的喹喔啉-2-酮的制备和生物学评价。第三部分

合成了在环系统C-3上带有各种侧链(烷基,卤代烷基,苄基和苯基)的一系列新的喹喔啉酮6 / 7-三氟甲基或硝基和6,7-二氟取代基,并准备在体外评估抗菌,抗真菌,抗分枝杆菌,抗癌和抗HIV活性。这些筛选的结果表明,化合物23-28显示出对各种念珠菌菌株的良好抑制活性。化合物24还显示出令人感兴趣的体外抗癌活性。
更新日期:2019-11-01
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