Pyrrolopyridazine MEK inhibitors.

Zhong Chen, Soong-Hoon Kim, Stephanie A Barbosa, Tram Huynh, David R Tortolani, Kenneth J Leavitt, Donna D Wei, Veeraswamy Manne, Carolyn S Ricca, Johnni Gullo-Brown, Michael A Poss, Wayne Vaccaro, Mark E Salvati
Author Information
  1. Zhong Chen: Bristol-Myers Squibb, Pharmaceutical Research Institute, PO Box 4000, Princeton, NJ 08543-4000, USA. zhong.chen@bms.com

Abstract

The synthesis and SAR of a series of pyrrolopyridazine MEK inhibitors are reported. Optimal activity was achieved by incorporation of a 4-phenoxyaniline substituent at C4 and an acylated amine at C6.

MeSH Term

Acylation
Amines
Aniline Compounds
Animals
Drug Design
Enzyme Inhibitors
Humans
Mitogen-Activated Protein Kinase Kinases
Pyridazines
Pyrroles
Rats
Structure-Activity Relationship

Chemicals

Amines
Aniline Compounds
Enzyme Inhibitors
Pyridazines
Pyrroles
Pyrrolopyridazine
pyridazine
Mitogen-Activated Protein Kinase Kinases
aniline

Word Cloud

Created with Highcharts 10.0.0MEKinhibitorssynthesisSARseriespyrrolopyridazinereportedOptimalactivityachievedincorporation4-phenoxyanilinesubstituentC4acylatedamineC6Pyrrolopyridazine

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