Asymmetric synthesis and biological evaluations of (+)- and (-)-6-dimethoxymethyl-1,4-dihydropyridine-3-carboxylic acid derivatives blocking N-type calcium channels

Bioorg Med Chem Lett. 2011 Jun 1;21(11):3317-9. doi: 10.1016/j.bmcl.2011.04.007. Epub 2011 Apr 9.

Abstract

An efficient asymmetric synthesis of 1,4-dihydropyridine derivatives is described. The key step is the stereoselective Michael addition using t-butyl ester of L-valine as a chiral auxiliary to achieve good ee (>95% for all the tested experiments) and moderate yield. With this method, (+)-4-(3-chlorophenyl)-6-dimethoxymethyl-2-methyl-1,4-dihydropyridine-3,5-dicarboxylic acid cinnamyl ester was obtained and was characterized as a promising N-type calcium channel blocker with improved selectivity over L-type compared to its (-)- and racemic isomers.

MeSH terms

  • Animals
  • Calcium Channels, N-Type / drug effects*
  • Carboxylic Acids / chemical synthesis*
  • Carboxylic Acids / chemistry
  • Carboxylic Acids / pharmacology*
  • Cell Line, Tumor
  • Dihydropyridines / chemical synthesis
  • Dihydropyridines / chemistry
  • Dihydropyridines / pharmacology
  • Humans
  • Methyl Ethers / chemical synthesis
  • Methyl Ethers / chemistry
  • Methyl Ethers / pharmacology
  • Molecular Structure
  • Protein Binding / drug effects
  • Rats
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • Calcium Channels, N-Type
  • Carboxylic Acids
  • Dihydropyridines
  • Methyl Ethers
  • 1,4-dihydropyridine