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SYNTHESIS AND CHARACTERIZATION OF SOME ISOXAZOLE DERIVATIVES FOR ANTIMICROBIAL ACTIVITY

机译:一些异恶唑衍生物的抗菌活性的合成与表征

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In the present work, some newer 3,5-substituted diphenyl isoxazole derivatives (compounds 1-10) were synthesised by reaction of hydroxylamine hydrochloride with various freshly synthesised 1-(substituted phenyl)-3-(substituted phenyl)prop-2en-1-one derivatives (compounds. 1A-10A) in the presence of pyridine and catalytic amount of sodium hydroxide. Compounds 2, 4, 5, 10 were found to possess good antibacterial activity and compounds 3 and 10 showed good antifungal activity when compared with standard drugs ciprofloxacin and fluconazole at the concentration 50 ug ml_1. These results suggest that the synthesized isoxazole derivatives exhibit promising activity and this work may pave the way for future development of promising compounds for this purpose.
机译:在本作工作中,通过将盐酸羟胺与各种新合成的1-(取代的苯基)-3-(取代的苯基)-3-(取代的苯基)-3-(取代的苯基)-3-(取代的苯基)-3-2EN 1反应合成了一些新的3,5-取代的二苯基异恶唑衍生物(化合物1-10) - 在吡啶和催化量的氢氧化钠存在下,衍生物(化合物。1A-10A)。 发现化合物2,4,5,10具有良好的抗菌活性和化合物3和10显示出与标准药物Ciprofloxacin和浓度50ug mL_1的氟康唑相比的良好的抗真菌活性。 这些结果表明,合成的异恶唑衍生物表现出有希望的活动,这项工作可以为此目的的未来发展的未来发展铺平道路。

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