Phosphonomethylphosphorylmethyl(oxy)-analogues of geranylgeranyl diphosphate as stable and selective geranylgeranyl protein transferase inhibitors

Farmaco. 2004 Nov;59(11):887-92. doi: 10.1016/j.farmac.2004.08.002.

Abstract

The diphosphate moiety of geranylgeranyldiphosphate (GGdP) was replaced with metabolically and hydrolytically stable analogous polar portions, in an attempt to obtain new geranylgeranyltransferase (GGTase) inhibitors, which could also be selective over congener enzyme farnesyltransferase (FTase). In particular, the phosphonomethylphosphorylmethoxy derivative showed the highest inhibition potency, accompanied by a satisfactory GGTase/FTase selectivity.

MeSH terms

  • Alkyl and Aryl Transferases / antagonists & inhibitors*
  • Diterpenes / chemical synthesis*
  • Diterpenes / pharmacology
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / pharmacology
  • Inhibitory Concentration 50
  • Organophosphorus Compounds / chemical synthesis*
  • Organophosphorus Compounds / pharmacology
  • Polyisoprenyl Phosphates / chemical synthesis*
  • Polyisoprenyl Phosphates / pharmacology

Substances

  • Diterpenes
  • Enzyme Inhibitors
  • Organophosphorus Compounds
  • Polyisoprenyl Phosphates
  • Alkyl and Aryl Transferases
  • geranylgeranyltransferase type-I
  • geranylgeranyl pyrophosphate