Synthesis and evaluation of a novel series of quinoline derivatives with immunosuppressive activity

Bioorg Med Chem. 2009 Aug 1;17(15):5433-41. doi: 10.1016/j.bmc.2009.06.043. Epub 2009 Jun 26.

Abstract

A series of quinoline derivatives were synthesized and their immunosuppressive activity and cytotoxicity were evaluated with a T-cell functional assay and MTT method, respectively. Most of 5,7-dimethoxyquinolin-4-yl ortho-substituted benzoate derivatives (18, 22, 24, 28, 31 and 37) showed a quite stronger inhibitory activity compared to other analogs. Among the synthesized compounds, 5,7-dimethoxyquinolin-4-yl 2,6-dichlorobenzoate (22) and 5,7-dimethoxyquinolin-4-yl 4-methylbenzenesulfonate (40) exhibited a potent inhibitory activity without significant cytotoxicity at 10 microM concentration. The preliminary mechanism of the active compounds 22 and 40 was further clarified based on the fluorescence activated cell sorter (FACS) assay, and the compounds exerted immunosuppressive activity via inhibiting the T cell activation in a dose dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation / drug effects*
  • Female
  • Immunosuppressive Agents / chemical synthesis
  • Immunosuppressive Agents / chemistry*
  • Immunosuppressive Agents / pharmacology*
  • Mice
  • Mice, Inbred BALB C
  • Molecular Structure
  • Quinolines / chemical synthesis
  • Quinolines / chemistry*
  • Quinolines / pharmacology*
  • Spleen / cytology
  • Structure-Activity Relationship
  • T-Lymphocytes / cytology
  • T-Lymphocytes / drug effects*

Substances

  • Immunosuppressive Agents
  • Quinolines