[Synthesis and immunosuppressive effects of novel phthalazine ketone derivatives]

Yao Xue Xue Bao. 2013 Oct;48(10):1579-84.
[Article in Chinese]

Abstract

A series of phthalazine ketone compounds were synthesized and the structures were confirmed by H NMR and HR-MS spectrum. All target compounds were obtained through 7 steps, including selective reduction, nitration, bromination, ring enlargement, reduction, Knoevenagel and acylated reaction. The compounds were evaluated for their immunosuppressive effects of T-cell proliferation and inhibitory activity of IMPDH type II in vitro, as well as their structure-activity relationship were assessed. Several compounds exhibited strong immunosuppressive properties, especially compounds 7f and 7h, with IC50 values of 0.093 micromol x L(-1) and 0.14 micromol x L(-1) respectively, which were superior to mycophenolic acid. The information obtained from the studies may be useful for further research on the immunosuppressive agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation / drug effects*
  • Female
  • IMP Dehydrogenase / metabolism
  • Immunosuppressive Agents / chemical synthesis*
  • Immunosuppressive Agents / chemistry
  • Immunosuppressive Agents / pharmacology
  • Inhibitory Concentration 50
  • Mice
  • Mice, Inbred BALB C
  • Phthalazines / chemical synthesis*
  • Phthalazines / chemistry
  • Phthalazines / pharmacology
  • Spleen / cytology
  • Structure-Activity Relationship
  • T-Lymphocytes / drug effects

Substances

  • Immunosuppressive Agents
  • Phthalazines
  • IMP Dehydrogenase
  • IMPDH2, mouse