Structure-activity relationships in a series of C2-substituted gluco-configured tetrahydroimidazopyridines as β-glucosidase inhibitors

Bioorg Med Chem. 2011 Apr 1;19(7):2136-44. doi: 10.1016/j.bmc.2011.02.043. Epub 2011 Feb 26.

Abstract

Inhibition of glycoside hydrolases has widespread application in treatment of diabetes, viral infections, lysosomal storage diseases and cancers. Gluco-configured tetrahydroimidazopyridines are the most potent β-glucosidase inhibitors reported to date. Using transition state mimic strategy, a series of C2-substituted gluco-configured tetrahydroimidazopyridines were designed and synthesized. Compounds 3 (K(i)=0.64 nM) and 5 (K(i)=0.58 nM) showed stronger inhibitory potency against β-glucosidase. Maestro 9.1 was used to study the structure-activity relationships by docking the compounds into the β-glucosidase active sites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology*
  • Imidazoles / chemistry
  • Imidazoles / pharmacology
  • Kinetics
  • Models, Molecular
  • Plant Extracts / antagonists & inhibitors
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Prunus / enzymology
  • Pyridines / chemistry*
  • Pyridines / pharmacology*
  • Stereoisomerism
  • Structure-Activity Relationship
  • beta-Glucosidase / antagonists & inhibitors*
  • beta-Glucosidase / chemistry

Substances

  • Enzyme Inhibitors
  • Imidazoles
  • Plant Extracts
  • Pyridines
  • beta-Glucosidase