Looking-glass synergistic pharmacological chaperones: DGJ and L-DGJ from the enantiomers of tagatose.

Journal article

The enantiomers of tagatose are converted to L-DGJ [a noncompetitive inhibitor of human lysosome α-galactosidase A (α-Gal A), K(i) 38.5 μM] and DGJ [a competitive inhibitor of α-Gal A, K(i) 15.1 nM] in 66% yield. L-DGJ and DGJ provide the first examples of pharmacological chaperones that (a) are enantiomeric iminosugars and (b) have synergistic activity with implications for the treatment of lysosomal storage disorders and other protein deficiencies.

Authors: Jenkinson, S; Fleet, G; Nash, R; Koike, Y; Adachi, I

• Publication status: Published
• Journal: Organic letters
• Volume: 13
• Issue: 15
• Pages: 4064-4067
• Publication date: 2011-08-01
• DOI: 10.1021/ol201552q
• EISSN: 1523-7052
• ISSN: 1523-7060
• Language: English
• Keywords: Hexoses; Humans; Lysosomes; Glass; Fibroblasts; Molecular Structure; Stereoisomerism; alpha-Galactosidase