Synthesis and biological activity of mycophenolic acid-amino acid derivatives

Eur J Med Chem. 2013 Nov:69:863-71. doi: 10.1016/j.ejmech.2013.09.026. Epub 2013 Sep 19.

Abstract

In search of new immunosuppressants we synthesized 11 amino acids derivatives of MPA as methyl esters 10a-k using EDCI/DMAP and their corresponding amino acid derivatives in free acid form 11a-k by hydrolysis of ester group with LiOH/MeOH. New analogs were evaluated as growth inhibitors of lymphoid cell line (Jurkat) and human peripheral blood mononuclear cells (PBMC) from healthy donors. According to obtained results recovering of free carboxylic group increased their activity. Additionally, the cytotoxic properties depends on the substituent and configuration at chiral center in amino acid unit. The compounds 10j, 11e and 11h exhibited higher potency than MPA 1 in vitro.

Keywords: Amino acid derivatives; Cytotoxic activity; IMPDH inhibitors; Mycophenolic acid derivatives.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemical synthesis
  • Amino Acids / chemistry
  • Amino Acids / pharmacology*
  • Amino Acids / toxicity
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Humans
  • Jurkat Cells
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / drug effects*
  • Molecular Structure
  • Mycophenolic Acid / chemical synthesis
  • Mycophenolic Acid / chemistry
  • Mycophenolic Acid / pharmacology*
  • Mycophenolic Acid / toxicity
  • Structure-Activity Relationship

Substances

  • Amino Acids
  • Mycophenolic Acid