Optimisation of a novel series of potent and orally bioavailable azanaphthyridine SYK inhibitors

Bioorg Med Chem Lett. 2016 Oct 1;26(19):4606-4612. doi: 10.1016/j.bmcl.2016.08.070. Epub 2016 Aug 23.

Abstract

The optimisation of the azanaphthyridine series of Spleen Tyrosine Kinase inhibitors is described. The medicinal chemistry strategy was focused on optimising the human whole blood activity whilst achieving a sufficient margin over hERG activity. A good pharmacokinetic profile was achieved by modification of the pKa. Morpholine compound 32 is a potent SYK inhibitor showing moderate selectivity, good oral bioavailability and good efficacy in the rat Arthus model but demonstrated a genotoxic potential in the Ames assay.

Keywords: Azanaphthyridine; Lead optimisation; Medicinal chemistry; Orally bioavailable; Potent; SYK; Selective; Spleen Tyrosine Kinase.

MeSH terms

  • Administration, Oral
  • Animals
  • Biological Availability
  • Crystallography, X-Ray
  • Humans
  • Mutagenicity Tests
  • Naphthyridines / administration & dosage
  • Naphthyridines / pharmacokinetics
  • Naphthyridines / pharmacology*
  • Protein Kinase Inhibitors / administration & dosage
  • Protein Kinase Inhibitors / pharmacokinetics
  • Protein Kinase Inhibitors / pharmacology*
  • Rats
  • Structure-Activity Relationship

Substances

  • Naphthyridines
  • Protein Kinase Inhibitors