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首页> 外文期刊>Scientific reports. >New α-glucosidase inhibitors from marine algae-derived Streptomyces sp. OUCMDZ-3434
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New α-glucosidase inhibitors from marine algae-derived Streptomyces sp. OUCMDZ-3434

机译:来自海洋藻类的新α-葡萄糖苷酶抑制剂 - 衍生的链霉菌 - sp。 OUCMDZ-3434.

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摘要

Wailupemycins H ( 1 ) and I ( 2 ) with a new skeleton coupled two 6-(2-phenylnaphthalene-1-yl)pyrane-2-one nuclei to a –CH2– linkage were identified from the culture of Streptomyces sp. OUCMDZ-3434 associated with the marine algae, Enteromorpha prolifera . Compounds 1 and 2 are two new α-glucosidase inhibitors with the Ki/IC50 values of 16.8/19.7 and 6.0/8.3 μ M, respectively. In addition, the absolute configurations of wailupemycins D ( 3 ) and E ( 4 ) are also resolved in this paper for the first time.
机译:Wailupemycins H(1)和I(2)具有新的骨架偶联两种6-(2-苯基萘-1-基)吡喃-2-一核,鉴定为-CH 2 - 键streptomyces sp的培养。 oucmdz-3434与海藻藻类相关,肠道藻藻植物。化合物1和2是两种新的α-葡萄糖苷酶抑制剂,其k i / in 50 值分别为16.8 / 19.7和6.0 / 8.0 / 8.0 / 8.0 / 8.0 / 8.0 / 8.0 /米。另外,第一次在本文中解析了Wailupmycins D(3)和E(4)的绝对配置。

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