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首页> 外文期刊>Bioorganic and medicinal chemistry >Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent alpha-glucosidase inhibitors.
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Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent alpha-glucosidase inhibitors.

机译:作为有效的α-葡萄糖苷酶抑制剂的硫糖基sulf盐,新花生米酚和新ponkoranol的分离,结构鉴定和SAR研究。

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摘要

Two hitherto missing members of sulfonium salts family in Salacia genus plants as a new class of alpha-glucosidase inhibitors, neoponkoranol (7) and neosalaprinol (8), were isolated from the water extracts, and their structures were unambiguously identified. For further SAR studies on this series of sulfonium salts, several epimers of 7 and 8 were synthesized, and their inhibitory activities against rat small intestinal alpha-glucosidases were evaluated. Among them, 3'-epimer of 7 was found most potent in this class of molecules, and revealed as potent as currently used antidiabetics, voglibose and acarbose.
机译:从水提取物中分离出褐藻属植物中迄今缺失的missing盐家族的两个成员,它们是一类新的α-葡萄糖苷酶抑制剂,新ponkoranol(7)和neasalaprinol(8),其结构得到明确鉴定。为了进一步研究该系列salts盐的SAR,合成了7和8的几种差向异构体,并评估了它们对大鼠小肠α-葡萄糖苷酶的抑制活性。其中,在此类分子中发现7的3'-末端最有效,并且显示出与当前使用的抗糖尿病药,伏格列波糖和阿卡波糖一样有效。

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