Pyrrolo[2,3-d]Pyrimidines as Kinase Inhibitors

Curr Med Chem. 2017;24(19):2059-2085. doi: 10.2174/0929867324666170303162100.

Abstract

The pyrrolo[2,3-d]pyrimidine nucleus is a deaza-isostere of adenine, the nitrogenous base of ATP, and is present in many ATP-competitive inhibitors of different kinases. In the last few years the number of articles and patents that have appeared involving this type of inhibitors has dramatically increased and some compounds have been approved for the treatment of inflammatory or myeloproliferative diseases. Other derivatives are currently being evaluated in clinical trials. This review deals with pyrrolo[2,3- d]pyrimidine derivatives active as kinase inhibitors that have been reported in the literature from 2011 to 2016, with a particular interest on the recently patented compounds. The molecules are classified depending on the inhibited kinase, focusing on their chemical structures.

Keywords: 3-d]pyrimidine; Pyrrolo[2; anti-inflammatory agents; anticancer agents; kinase inhibitors; patents.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Drug Design
  • Humans
  • Inflammation / drug therapy
  • Inflammation / enzymology
  • Molecular Docking Simulation
  • Neoplasms / drug therapy
  • Neoplasms / enzymology
  • Protein Kinase Inhibitors / chemistry*
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Pyrimidines / chemistry*
  • Pyrimidines / pharmacology*
  • Pyrimidines / therapeutic use
  • Pyrroles / chemistry*
  • Pyrroles / pharmacology*
  • Pyrroles / therapeutic use
  • Structure-Activity Relationship

Substances

  • Anti-Inflammatory Agents
  • Antineoplastic Agents
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Pyrroles