LipE guided discovery of isopropylphenyl pyridazines as pantothenate kinase modulators

Bioorg Med Chem. 2021 Dec 15:52:116504. doi: 10.1016/j.bmc.2021.116504. Epub 2021 Nov 12.

Abstract

Pantothenate kinase (PANK) is the critical regulator of intracellular levels of coenzyme A and has emerged as an attractive target for treating neurological and metabolic disorders. This report describes the optimization, synthesis, and full structure-activity relationships of a new chemical series of pantothenate competitive PANK inhibitors. Potent drug-like molecules were obtained by optimizing a high throughput screening hit, using lipophilic ligand efficiency (LipE) derived from human PANK3 IC50 values to guide ligand development. X-ray crystal structures of PANK3 with index inhibitors from the optimization were determined to rationalize the emerging structure activity relationships. The analysis revealed a key bidentate hydrogen bonding interaction between pyridazine and R306' as a major contributor to the LipE gain observed in the optimization. A tractable series of PANK3 modulators with nanomolar potency, excellent LipE values, desirable physicochemical properties, and a well-defined structural binding mode was produced from this study.

Keywords: Hit-to-lead; Lipophilic ligand efficiency; Pantothenate Kinase; Pyridazine.

Publication types

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

MeSH terms

  • Dose-Response Relationship, Drug
  • Drug Discovery*
  • High-Throughput Screening Assays*
  • Humans
  • Hydrogen Bonding
  • Ligands
  • Molecular Structure
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism*
  • Pyridazines / chemical synthesis
  • Pyridazines / chemistry
  • Pyridazines / pharmacology*
  • Structure-Activity Relationship

Substances

  • Ligands
  • Pyridazines
  • Phosphotransferases (Alcohol Group Acceptor)
  • pantothenate kinase