2-氨基吡啶内酯的合成及其抗氧化、抗菌和抗真菌性能研究

ECSOC-25 Pub Date : 2021-11-15 DOI:10.3390/ecsoc-25-11709
Fadila Salhi, N. Cheikh, D. Villemin, N. Bar
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引用次数: 0

摘要

本文研究了取代2-氨基吡啶δ -内酯衍生物的合成及其生物活性。以4-羟基-4-甲基戊烷-2- 1为原料合成4,6,6-三甲基-2-氧-5,6-二氢- 2h -吡喃-3-碳腈,然后用DMFDMA在氨基腈中转化。DPPH法评价了取代2-氨基吡啶δ -内酯衍生物的抗氧化作用,发现其具有较强的抗氧化能力。采用圆盘扩散法研究其对临床革兰氏阴性菌和临床真菌的抑菌活性。研究表明,新取代的2-氨基吡啶δ -内酯衍生物具有中等到极好的抗菌和抗真菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of 2-aminopyridine Lactones and Studies of Their Antioxidant, Antibacterial and Antifungal Properties
: In the present work, the synthesis and biological activities of substituted 2-aminopyridine δ -lactone derivatives were achieved. 4,6,6-trimethyl-2-oxo-5,6-dihydro-2H-pyran-3-carbonitrile was synthesised from 4-hydroxy-4-methylpentan-2-one, followed by its transformation in enaminonitrile with DMFDMA. The antioxidant effects of substituted 2- aminopyridine δ -lactone derivatives were evaluated through DPPH assay and revealed a great antioxidant capacity. The antifungal and antibacterial activities were investigated by disc diffusion method against clinical Gram-nega-tive bacteria and against clinical fungi. The study shows moderate to very good antibacterial and antifungal activities for the new substituted 2- aminopyridine δ -lactone derivatives .
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