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赞比亚黄木中的夫糖胺异构体和糖苷。

Fagomine isomers and glycosides from Xanthocercis zambesiaca.

作者信息

Kato A, Asano N, Kizu H, Matsui K

机构信息

Faclty of Pharmaceuitcal Sciences, Hokuriku University, Japan.

出版信息

J Nat Prod. 1997 Mar;60(3):312-4. doi: 10.1021/np960646y.

Abstract

50% aqueous MeOH extracts from the leaves and roots of Xanthocercis zambesiaca (Leguminosae) were subjected to various ion-exchange column chromatographic steps to give fagomine (1), 3-epi-fagomine (2), 3,4-di-epi-fagomine (3), 3-O-beta-D-glucopyranosylfagomine (4), and 4-O-beta-D-glucopyranosylfagomine (5). Their structures were determined by spectroscopic analyses, particularly by extensive 1D and 2D NMR studies. Compounds 3 and 4 are new natural products. Compound 1 is a good inhibitor of isomaltase and certain alpha- and beta-galactosidases. Whereas 2 is a more potent inhibitor of isomaltase and beta-galactosidases than 1, it does not inhibit alpha-galactosidase. Compounds 3-5 exhibited no significant inhibition against the glycosidases used.

摘要

对赞比亚黄木犀(豆科)叶和根的50%甲醇水溶液提取物进行了各种离子交换柱色谱步骤,得到了法戈明(1)、3-表-法戈明(2)、3,4-二表-法戈明(3)、3-O-β-D-吡喃葡萄糖基法戈明(4)和4-O-β-D-吡喃葡萄糖基法戈明(5)。通过光谱分析,特别是广泛的一维和二维核磁共振研究确定了它们的结构。化合物3和4是新的天然产物。化合物1是异麦芽糖酶以及某些α-和β-半乳糖苷酶的良好抑制剂。虽然2是比1更有效的异麦芽糖酶和β-半乳糖苷酶抑制剂,但它不抑制α-半乳糖苷酶。化合物3-5对所使用的糖苷酶没有显著抑制作用。

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