| Literature DB >> 21441415 |
Jean Christophe Hau1, Patrizia Fontana, Catherine Zimmermann, Alain De Pover, Dirk Erdmann, Patrick Chène.
Abstract
The development of new drugs with better pharmacological and safety properties mandates the optimization of several parameters. Today, potency is often used as the sole biochemical parameter to identify and select new molecules. Surprisingly, thermodynamics, which is at the core of any interaction, is rarely used in drug discovery, even though it has been suggested that the selection of scaffolds according to thermodynamic criteria may be a valuable strategy. This poor integration of thermodynamics in drug discovery might be due to difficulties in implementing calorimetry experiments despite recent technological progress in this area. In this report, the authors show that fluorescence-based thermal shift assays could be used as prescreening methods to identify compounds with different thermodynamic profiles. This approach allows a reduction in the number of compounds to be tested in calorimetry experiments, thus favoring greater integration of thermodynamics in drug discovery.Mesh:
Substances:
Year: 2011 PMID: 21441415 DOI: 10.1177/1087057111399573
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571