Dinucleoside polyphosphate NAD analogs as potential NMN adenylyltransferase inhibitors. Synthesis and biological evaluation

Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):865-8. doi: 10.1081/NCN-120022673.

Abstract

Two dinucleoside polyphosphate NAD analogs, P1-(adenosine-5')-P3-(nicotinamide riboside-5')triphosphate (Np3A, 1) and P1-(adenosine-5')-P4-(nicotinamide riboside-5')tetraphosphate (Np4A, 2), were synthesized and tested as inhibitors of both microbial and human recombinant NMN adenylyltransferase. Compounds 1 and 2 proved to be selective inhibitors of microbial enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Enzyme Inhibitors / chemical synthesis*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology
  • Humans
  • NAD / analogs & derivatives*
  • NAD / chemical synthesis*
  • NAD / chemistry
  • NAD / pharmacology
  • Nicotinamide-Nucleotide Adenylyltransferase / antagonists & inhibitors*
  • Recombinant Proteins / antagonists & inhibitors

Substances

  • Enzyme Inhibitors
  • Recombinant Proteins
  • NAD
  • Nicotinamide-Nucleotide Adenylyltransferase