Integrating fragment assembly and biophysical methods in the chemical advancement of small-molecule antagonists of IL-2: an approach for inhibiting protein-protein interactions

J Med Chem. 2004 Jun 3;47(12):3111-30. doi: 10.1021/jm049967u.

Abstract

Fragment assembly has shown promise for discovering small-molecule antagonists for difficult targets, including protein-protein interactions. Here, we describe a process for identifying a 60 nM inhibitor of the interleukin-2 (IL-2)/IL-2 receptor (IL-2Ralpha) interaction. By use of fragment-based approaches, a compound with millimolar affinity was evolved to a hit series with low micromolar activity, and these compounds were optimized into a lead series with nanomolar affinity. Fragment assembly was useful not only for hit identification, but also for lead optimization. Throughout the discovery process, biophysical methods and structural biology demonstrated that compounds bound reversibly to IL-2 at the IL-2 receptor binding site.

MeSH terms

  • Acetylene / chemical synthesis*
  • Acetylene / chemistry
  • Acetylene / pharmacology
  • Animals
  • Benzene Derivatives / chemistry
  • Binding Sites
  • Combinatorial Chemistry Techniques
  • Crystallography, X-Ray
  • Dipeptides / chemical synthesis*
  • Dipeptides / chemistry
  • Dipeptides / pharmacology
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Interleukin-2 / antagonists & inhibitors*
  • Interleukin-2 / chemistry
  • Interleukin-2 Receptor alpha Subunit
  • Mice
  • Models, Molecular
  • Piperidines / chemistry
  • Pyrazoles / chemistry
  • Receptors, Interleukin / antagonists & inhibitors*
  • Receptors, Interleukin / chemistry

Substances

  • Benzene Derivatives
  • Dipeptides
  • IL2RA protein, human
  • Il2ra protein, mouse
  • Interleukin-2
  • Interleukin-2 Receptor alpha Subunit
  • Piperidines
  • Pyrazoles
  • Receptors, Interleukin
  • Acetylene