Title of article :
β-C-Glycosiduronic acids and β-C-glycosyl compounds: New PTP1B inhibitors
Author/Authors :
Li Lin، نويسنده , , Qiang Shen، نويسنده , , Guorong Chen، نويسنده , , Li Juan Xie، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Abstract :
β-C-Glycosiduronic acid quinones and β-C-glycosyl compounds have been synthesized as sugar-based PTP1B inhibitors. Benzoyl protected quinone derivatives (14 and 35) as well as aryl β-C-glycosyl compounds (18, 22, 23 and 34) showed IC50 values of 0.77–5.27 μM against PTP1B, with compounds 18 and 23 bearing an acidic function being the most potent.
Keywords :
inhibitor , Diabetes , C-Glycosyl compounds , Quinone , Uronic acid , Protein tyrosine phosphatase 1B
Journal title :
Bioorganic & Medicinal Chemistry Letters
Journal title :
Bioorganic & Medicinal Chemistry Letters