R-stereopreference analysis of lipase Novozym 435 in kinetic resolution of flurbiprofen

Chirality. 2007 May 5;19(4):245-9. doi: 10.1002/chir.20347.

Abstract

Immobilized lipase from Candida antarctica (Novozym 435) was employed in the kinetic resolution of racemic flurbiprofen by enantioselective esterification with methanol. It was found that the lipase has the R-stereopreference and the reaction matches Bi Bi Ping Pong mechanism with dead-end inhibition of methanol. Furthermore, the R-stereopreference was analyzed in details from the aspects of enzymatic kinetic mechanism and reaction activation energy of both enantiomers. The R-enantiomer shows lower activation energy and higher maximum reaction rate than the S-enantiomer, which implies the R-stereopreference of the lipase and makes the kinetic resolution of flurbiprofen via enzymatic reaction feasible.

MeSH terms

  • Candida / enzymology
  • Carbonic Anhydrase Inhibitors / chemistry
  • Dose-Response Relationship, Drug
  • Enzymes, Immobilized / chemistry
  • Esterification
  • Flurbiprofen / chemistry*
  • Fungal Proteins
  • Kinetics
  • Lipase / chemistry*
  • Methanol / chemistry
  • Models, Chemical
  • Models, Statistical
  • Models, Theoretical
  • Stereoisomerism
  • Temperature

Substances

  • Carbonic Anhydrase Inhibitors
  • Enzymes, Immobilized
  • Fungal Proteins
  • Flurbiprofen
  • Novozyme 435
  • Lipase
  • Methanol