Non-thiazolidinedione antihyperglycaemic agents. Part 3: The effects of stereochemistry on the potency of alpha-methoxy-beta-phenylpropanoic acids

Bioorg Med Chem. 1999 May;7(5):821-30. doi: 10.1016/s0968-0896(99)00034-6.

Abstract

Rhizopus delemar lipase catalysed ester hydrolysis of the alpha-methoxy-beta-phenylpropanoate 1 affords the (R)-(+) and (S)-(-) isomers in > 84% enantiomeric excess. Absolute stereochemistry was determined by a single crystal X-ray analysis of a related synthetic analogue. The activity of these two enantiomers on glucose transport in vitro and as anti-diabetic agents in vivo is reported and their unexpected equivalence attributed to an enzyme-mediated stereospecific isomerisation of the (R)-(+) isomer. Binding studies using recombinant human PPARgamma (peroxisomal proliferator activated receptor gamma), now established as a molecular target for this compound class, indicate a 20-fold higher binding affinity for the (S) antipode relative to the (R) antipode.

MeSH terms

  • Animals
  • Crystallography, X-Ray
  • Hypoglycemic Agents / chemical synthesis*
  • Hypoglycemic Agents / pharmacology*
  • Models, Chemical
  • Models, Molecular
  • Phenylpropionates / chemical synthesis*
  • Rats
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Stereoisomerism
  • Time Factors
  • Transcription Factors / metabolism

Substances

  • Hypoglycemic Agents
  • Phenylpropionates
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors