Tuning glycosidase inhibition through aglycone interactions: pharmacological chaperones for Fabry disease and GM1 gangliosidosis.

نویسندگان

  • M Aguilar-Moncayo
  • T Takai
  • K Higaki
  • T Mena-Barragán
  • Y Hirano
  • K Yura
  • L Li
  • Y Yu
  • H Ninomiya
  • M I García-Moreno
  • S Ishii
  • Y Sakakibara
  • K Ohno
  • E Nanba
  • C Ortiz Mellet
  • J M García Fernández
  • Y Suzuki
چکیده

Competitive inhibitors of either α-galactosidase (α-Gal) or β-galactosidase (β-Gal) with high affinity and selectivity have been accessed by exploiting aglycone interactions with conformationally locked sp(2)-iminosugars. Selected compounds were profiled as potent pharmacological chaperones for mutant lysosomal α- and β-Gal associated with Fabry disease and GM(1) gangliosidosis.

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عنوان ژورنال:
  • Chemical communications

دوره 48 52  شماره 

صفحات  -

تاریخ انتشار 2012