Synthesis and Biological Evaluation of 3-Arylindazoles as Selective MEK4 Inhibitors

Kristine K. Deibler, Gary E Schiltz, Matt Clutter, Rama K Mishra, Purav P. Vagadia, Matthew O'Connor, Mariam Donny George, Ryan Gordon, Graham Fowler, Raymond Bergan, Karl A Scheidt*

*Corresponding author for this work

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Herein we report the discovery of a novel series of highly potent and selective mitogen-activated protein kinase kinase 4 (MEK4) inhibitors. MEK4 is an upstream kinase in MAPK signaling pathways that phosphorylates p38 MAPK and JNK in response to mitogenic and cellular stress queues. MEK4 is overexpressed and induces metastasis in advanced prostate cancer lesions. However, the value of MEK4 as an oncology target has not been pharmacologically validated because selective chemical probes targeting MEK4 have not been developed. Optimization of this series via structure–activity relationships and molecular modeling led to the identification of compound 6 ff (4-(6-fluoro-2H-indazol-3-yl)benzoic acid), a highly potent and selective MEK4 inhibitor. This series of inhibitors is the first of its kind in both activity and selectivity and will be useful in further defining the role of MEK4 in prostate and other cancers.

Original languageEnglish (US)
Pages (from-to)615-620
Number of pages6
JournalChemMedChem
Volume14
Issue number6
DOIs
StatePublished - Mar 22 2019

Keywords

  • MEK4
  • antitumor agents
  • indazoles
  • kinases
  • prostate cancer

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Pharmacology
  • Drug Discovery
  • Pharmacology, Toxicology and Pharmaceutics(all)
  • Organic Chemistry

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