Design of purine nucleoside phosphorylase inhibitors

Fed Proc. 1986 Nov;45(12):2773-8.

Abstract

Purine nucleoside phosphorylase inhibitors hold promise as specific immunosuppressive, anti-T cell leukemic, and antiuricopoietic agents. The best inhibitors available that are biologically active have Ki values from 10(-6) to 10(-7) M and fall into two categories: noncleavable nucleosides preferably iodinated at the C-5' position and C-8-substituted guanine or acycloguanosines. More potent inhibition is shown by phosphorylated acyclonucleosides that function as multisubstrate analogs, but these compounds are excluded from cells. The X-ray analysis of the human erythrocytic enzyme is beginning to reveal the nature of the active site and to explain the structure-activity relationships that have been established with analog substrates and inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Humans
  • Kinetics
  • Pentosyltransferases / antagonists & inhibitors*
  • Phosphorylation
  • Protein Conformation
  • Purine-Nucleoside Phosphorylase / antagonists & inhibitors*
  • Purine-Nucleoside Phosphorylase / deficiency
  • Structure-Activity Relationship
  • X-Ray Diffraction

Substances

  • Pentosyltransferases
  • Purine-Nucleoside Phosphorylase