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首页> 外文期刊>Bioorganic and medicinal chemistry >A facile synthesis of D-glucose-type gem-diamine 1-N-iminosugars: a new family of glucosidase inhibitors.
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A facile synthesis of D-glucose-type gem-diamine 1-N-iminosugars: a new family of glucosidase inhibitors.

机译:D-葡萄糖型宝石二胺1-N-亚氨基糖的简便合成:一种新的葡萄糖苷酶抑制剂家族。

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摘要

gem-Diamine 1-N iminosugars of D-glucose-type, a new type of glycosidase inhibitors, have been synthesized from siastatin B, isolated from Streptomyces culture. 2-Trifluoroacetamido-1-N-iminosugar, (2S,3R,4R,5R)-2-trifluoroacetamido-5-hydroxymethylpiperidine -3,4-diol was proved to be a potent inhibitor for alpha-D- and beta-D-glucosidases (IC50 1.9x10(-7) and 4.2x10(-7) M, respectively). 2-Acetamido-1-N-iminosugar, (2S,3R,4R,5R)-2-acetamido-5-hydroxymethylpiperidine-3,4-diol also affected these enzymes (IC50 2.9x10(-6) and 5.4x10(-6) M, respectively).
机译:D-葡萄糖类型的gem-Diamine 1-N亚氨基糖,一种新型的糖苷酶抑制剂,是从从链霉菌培养物中分离的siastatin B合成的。已证明2-三氟乙酰氨基-1-N-亚氨基糖,(2S,3R,4R,5R)-2-三氟乙酰氨基-5-羟甲基哌啶-3,4-二醇是α-D-和β-D-的有效抑制剂葡糖苷酶(IC50分别为1.9x10(-7)和4.2x10(-7)M)。 2-乙酰胺基-1-N-亚氨基糖,(2S,3R,4R,5R)-2-乙酰氨基-5-羟甲基哌啶-3,4-二醇也影响这些酶(IC50 2.9x10(-6)和5.4x10(- 6)M)。

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