3-cyanoindole-based inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure-activity relationships

Bioorg Med Chem Lett. 2003 Oct 20;13(20):3557-60. doi: 10.1016/s0960-894x(03)00757-1.

Abstract

A series of novel small molecule inhibitors of inosine monophosphate dehydrogenase (IMPDH), based upon a 3-cyanoindole core, were explored. IMPDH catalyzes the rate determining step in guanine nucleotide biosynthesis and is a target for anticancer, immunosuppressive and antiviral therapy. The synthesis and the structure-activity relationships (SAR), derived from in vitro studies, for this new series of inhibitors is given.

MeSH terms

  • Catalysis
  • Enzyme Inhibitors / pharmacology*
  • IMP Dehydrogenase / antagonists & inhibitors*
  • Indoles / pharmacology*
  • Kinetics
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • Indoles
  • IMP Dehydrogenase