Incorporation of rapid thermodynamic data in fragment-based drug discovery

J Med Chem. 2013 Mar 14;56(5):2155-9. doi: 10.1021/jm301603n. Epub 2013 Feb 27.

Abstract

Fragment-based drug discovery (FBDD) has enjoyed increasing popularity in recent years. We introduce SITE (single-injection thermal extinction), a novel thermodynamic methodology that selects high-quality hits early in FBDD. SITE is a fast calorimetric competitive assay suitable for automation that captures the essence of isothermal titration calorimetry but using significantly fewer resources. We describe the principles of SITE and identify a novel family of fragment inhibitors of the enzyme ketosteroid isomerase displaying high values of enthalpic efficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calorimetry / methods
  • Drug Discovery / methods*
  • Enzyme Inhibitors / chemical synthesis*
  • Enzyme Inhibitors / isolation & purification
  • Small Molecule Libraries*
  • Steroid Isomerases / antagonists & inhibitors*
  • Surface Plasmon Resonance
  • Thermodynamics*

Substances

  • Enzyme Inhibitors
  • Small Molecule Libraries
  • Steroid Isomerases
  • steroid delta-isomerase

Associated data

  • PDB/3VSY