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The effect of heteroatom substitution of sulfur for selenium in glucosidase inhibitors on intestinal α-glucosidase activities

机译:葡萄糖苷酶抑制剂中硫的杂原子取代硒对肠道α-葡萄糖苷酶活性的影响

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摘要

The synthesis of selenium analogues of de-O-sulfonated ponkoranol, a naturally occurring sulfonium-ion glucosidase inhibitor isolated from Salacia reticulata, and their evaluation as glucosidase inhibitors against two recombinant intestinal enzymes maltase glucoamylase (MGAM) and sucrase isomaltase (SI) are described.
机译:描述了脱O-磺化ponkoranol的硒类似物的合成,这是一种从网状海藻中分离的天然sulf离子葡糖苷酶抑制剂,并被评估为针对两种重组肠酶麦芽糖酶葡糖淀粉酶(MGAM)和蔗糖异麦芽糖酶(SI)的葡糖苷酶抑制剂。 。

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  • 来源
    《Chemical Communications》 |2011年第32期|p.9134-9136|共3页
  • 作者单位

    Department of Chemistry, Simon Fraser University, Burnaby,British Colombia, Canada V5A 1S6;

    Department of Biology, University of Waterloo, Waterloo, Ontario,Canada N2L 3G1;

    Department of Biology, University of Waterloo, Waterloo, Ontario,Canada N2L 3G1;

    Department of Chemistry, Simon Fraser University, Burnaby,British Colombia, Canada V5A 1S6;

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  • 入库时间 2022-08-17 13:22:40

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