Synthesis and Structural Revision of Glyphaeaside C
收藏NIAID Data Ecosystem2026-03-12 收录
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https://figshare.com/articles/dataset/Synthesis_and_Structural_Revision_of_Glyphaeaside_C/14519208
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资源简介：
The iminosugar core of natural glyphaeaside
C, originally assigned
as a derivative of the piperidine natural product 1-deoxynojirimycin
(DNJ), has been revised as a derivative of 2,5-dideoxy-2,5-imino-l-mannitol (l-DMDP) by the total synthesis of its enantiomer.
This revised l-DMDP-derived configuration is the first of
its kind to be observed in nature. The prepared iminosugars displayed
the nanomolar inhibition of bovine liver β-glucosidase and β-galactosidase.
创建时间：
2021-04-30
