Search for alpha-glucosidase inhibitors: new N-substituted valienamine and conduramine F-1 derivatives

Bioorg Med Chem. 2006 Sep 15;14(18):6255-82. doi: 10.1016/j.bmc.2006.05.080. Epub 2006 Jun 22.

Abstract

A solid-phase synthesis of new N-substituted valienamines has been developed and new synthesis of (+/-)-conduramine F-1, (-)-conduramine F-1, and (+)-ent-conduramine F-1 is presented, together with the preparation of N-benzylated conduramines F-1. N-Benzylation of both valienamine and (+)-ent-conduramine F-1 improves their inhibitory activity toward alpha-glucosidases significantly. The additional hydroxymethyl group makes valienamine derivatives more active than their (+)-ent-conduramine F-1 analogues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclohexanols / chemical synthesis
  • Cyclohexanols / chemistry
  • Cyclohexanols / pharmacology*
  • Cyclohexenes
  • Cyclohexylamines / chemical synthesis
  • Cyclohexylamines / chemistry
  • Cyclohexylamines / pharmacology*
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Glycoside Hydrolase Inhibitors*
  • Hexosamines / chemical synthesis
  • Hexosamines / chemistry
  • Hexosamines / pharmacology*
  • Molecular Structure
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • 6-aminocyclohex-4-ene-1,2,3-triol
  • Cyclohexanols
  • Cyclohexenes
  • Cyclohexylamines
  • Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • Hexosamines
  • valienamine