Discovery of cyclic guanidine-linked sulfonamides as inhibitors of LMTK3 kinase

Bioorg Med Chem Lett. 2020 May 1;30(9):127108. doi: 10.1016/j.bmcl.2020.127108. Epub 2020 Mar 17.

Abstract

Lemur tyrosine kinase 3 (LMTK3) is oncogenic in various cancers. In breast cancer, LMTK3 phosphorylates and modulates the activity of estrogen receptor-α (ERα) and is essential for the growth of ER-positive cells. LMTK3 is highly expressed in ER-negative breast cancer cells, where it promotes invasion via integrin β1. LMTK3 abundance and/or high nuclear expression have been linked to shorter disease free and overall survival time in a variety of cancers, supporting LMTK3 as a potential target for anticancer drug development. We sought to identify small molecule inhibitors of LMTK3 with the ultimate goal to pharmacologically validate this kinase as a novel target in cancer. We used a homogeneous time resolve fluorescence (HTRF) assay to screen a collection of mixture-based combinatorial chemical libraries containing over 18 million compounds. We identified several cyclic guanidine-linked sulfonamides with sub-micromolar activity and evaluated their binding mode using a 3D homology model of the LMTK3 KD.

Keywords: Breast cancer; Combinatorial chemistry; Guanidine-linked sulfonamide; LMTK3; Small molecule kinase inhibitors; Solid-phase synthesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Combinatorial Chemistry Techniques
  • Drug Discovery
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Humans
  • Membrane Proteins / antagonists & inhibitors*
  • Molecular Structure
  • Neoplasms / metabolism*
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Small Molecule Libraries
  • Sulfonamides / chemistry*
  • Sulfonamides / pharmacology*

Substances

  • Antineoplastic Agents
  • Membrane Proteins
  • Small Molecule Libraries
  • Sulfonamides
  • LMTK3 protein, human
  • Protein Serine-Threonine Kinases