Novel carbocyclic nucleoside analogs suppress glomerular mesangial cells proliferation and matrix protein accumulation through ROS-dependent mechanism in the diabetic milieu. II. Acylhydrazone-functionalized pyrimidines

Bioorg Med Chem Lett. 2016 Feb 1;26(3):1020-1024. doi: 10.1016/j.bmcl.2015.12.042. Epub 2015 Dec 12.

Abstract

We report herein the synthesis of a novel series of carbocyclic acylhydrazone derivatives of uracil, thymine and cytosine from the corresponding nucleic bases and their biological activity to treat diabetic nephropathy. Intriguingly, five derivatives significantly reduced high-glucose induced glomerular mesangial cells proliferation and matrix protein accumulation in vitro. The anti-oxidative effects displayed by these molecules suggest that their activity might involve a ROS-dependent mechanism.

Keywords: Acylhydrazones; Carbocyclic nucleosides; Cytosine; Diabetic nephropathy; Thymine; Uracil.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / pathology
  • Fibronectins / metabolism
  • Glucose / pharmacology
  • Mesangial Cells / cytology
  • Mesangial Cells / drug effects
  • Mesangial Cells / metabolism
  • Nucleosides / chemical synthesis
  • Nucleosides / chemistry*
  • Nucleosides / pharmacology
  • Pyrimidines / chemical synthesis
  • Pyrimidines / chemistry*
  • Pyrimidines / pharmacology
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • Actins
  • Fibronectins
  • Nucleosides
  • Pyrimidines
  • Reactive Oxygen Species
  • Glucose