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Design of Aminobenzothiazole Inhibitors of Rho Kinases 1 and 2 by Using Protein Kinase A as a Structure Surrogate.

Russell A JudgeAnil VasudevanVictoria E ScottGricelda H SimlerSteve D PrattMarian T NamovicC Brent PutmanAna AguirreVincent S StollMulugeta MamoSteven I SwannSteven C CassarConnie R FaltynekKaren L KageJanel M Boyce-RustayAdrian D Hobson
Published in: Chembiochem : a European journal of chemical biology (2018)
We describe the design, synthesis, and structure-activity relationships (SARs) of a series of 2-aminobenzothiazole inhibitors of Rho kinases (ROCKs) 1 and 2, which were optimized to low nanomolar potencies by use of protein kinase A (PKA) as a structure surrogate to guide compound design. A subset of these molecules also showed robust activity in a cell-based myosin phosphatase assay and in a mechanical hyperalgesia in vivo pain model.
Keyphrases
  • protein kinase
  • neuropathic pain
  • chronic pain
  • high throughput
  • single cell
  • cell therapy
  • pain management
  • stem cells
  • spinal cord injury
  • binding protein
  • bone marrow
  • postoperative pain