Exploring a cascade Heck-Suzuki reaction based route to kinase inhibitors using design of experiments

Org Biomol Chem. 2015 Mar 21;13(11):3382-92. doi: 10.1039/c4ob02694b.

Abstract

Design of Experiments (DoE) has been used to optimize a diversity oriented palladium catalyzed cascade Heck-Suzuki reaction for the construction of 3-alkenyl substituted cyclopenta[b]indole compounds. The obtained DoE model revealed a reaction highly dependent on the ligand. Guided by the model, an optimal ligand was chosen that selectively delivered the desired products in high yields. The conditions were applicable with a variety of boronic acids and were used to synthesize a library of 3-alkenyl derivatized compounds. Focusing on inhibition of kinases relevant for combating melanoma, the library was used in an initial structure-activity survey. In line with the observed kinase inhibition, cellular studies revealed one of the more promising derivatives to inhibit cell proliferation via an apoptotic mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Catalysis
  • Cell Proliferation / drug effects
  • Dose-Response Relationship, Drug
  • Drug Design*
  • Humans
  • Indoles / chemical synthesis
  • Indoles / chemistry
  • Indoles / pharmacology*
  • Leukocytes, Mononuclear / drug effects*
  • Molecular Structure
  • Palladium / chemistry
  • Phenols / chemical synthesis
  • Phenols / chemistry
  • Phenols / pharmacology*
  • Phosphotransferases / antagonists & inhibitors*
  • Phosphotransferases / metabolism
  • Protein Kinase Inhibitors / chemical synthesis*
  • Protein Kinase Inhibitors / chemistry
  • Structure-Activity Relationship

Substances

  • Indoles
  • Phenols
  • Protein Kinase Inhibitors
  • scytonemin
  • Palladium
  • Phosphotransferases