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Synthesis and Antimicrobial Activity of Phthalide Derivatives of Cytisine, Anabasine, and Salsoline
Chemistry of Natural Compounds ( IF 0.8 ) Pub Date : 2023-11-10 , DOI: 10.1007/s10600-023-04213-2
O. A. Nurkenov , S. D. Fazylov , Zh. S. Nurmaganbetov , T. M. Seilkhanov , R. B. Seidakhmetova , Z. M. Muldakhmetov , A. M. Gazaliev

Aminophthalide derivatives of cytisine, anabasine, and salsoline were obtained in high yields via condensation of the alkaloids with o-formylbenzoic acid. Their structures were proven using 1H and 13C NMR spectroscopy and data from 2D COSY 1H–1H and HMQC 1H–13C spectra. Studies of their antimicrobial activity showed moderate antimicrobial activity of 3-(N-cytisin-1-yl)isobenzofuran-1(3H)-one and 3-(N-salsolin-1-yl)isobenzofuran-1(3H)-one against Gram-positive test strain Staphylococcus aureus ATCC 6538 and Gram-negative test strain Escherichia coli ATCC 25922.



中文翻译:

金雀花碱、新木木碱和猪毛菜碱的苯并呋喃衍生物的合成及抗菌活性

通过生物碱与邻甲酰基苯甲酸的缩合,高产率地获得了金雀花碱、新木香和猪油碱的氨基苯酞衍生物。使用1 H 和13 C NMR 光谱以及 2D COSY 1 H– 1 H 和 HMQC 1 H– 13 C 光谱数据证明了它们的结构。其抗菌活性研究表明,3-( N-金雀花素-1-基)异苯并呋喃-1(3H ) -一和3-( N -salsolin-1-基)异苯并呋喃-1(3H ) -具有中等抗菌活性一种针对革兰氏阳性测试菌株金黄色葡萄球菌ATCC 6538 和革兰氏阴性测试菌株大肠杆菌ATCC 25922。

更新日期:2023-11-11
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