BioFocus DPI Launches Compound Library Targeting Protein-Protein Interactions Plus Three New Kinase Libraries

20 Sept 2009
Sarah Sarah
Marketing / Sales

Product news

BioFocus DPI today announced the launch of four new biologically targeted libraries. These new libraries contain novel, drug-like compounds that specifically target kinases and - for the first time - protein-protein interactions.

BioFocus DPI’s new Helix Mimetic library (HM01) is based on a novel structural motif that interacts with protein helices. This library is designed specifically to inhibit protein-protein interactions, but also targets other helical recognition motifs such as the pore region of ion channels.

BioFocus DPI’s three new SoftFocus® kinase libraries (SFK58, SFK59 and SFK60) target either the hinge region or novel binding modes. The SFK collection has been independently determined to have the greatest population of kinase-like molecules available for screening.

“Ten years after the launch of our first SoftFocus® kinase library, we are proud to launch our 100th focused library, HM01,” said Chris Newton, SVP BioFocus DPI. “This protein-protein interaction library is a reflection of our constantly evolving approach to library design, thereby providing clients with cutting-edge tools to accelerate drug discovery”.

Tags

Data MiningData mining is an important process for extracting information, patterns and trends from data. Data mining software, databases, reference materials and storage packages are available to process lab data.Compound LibrariesCompound libraries, or chemical libraries, are used in drug discovery for the identification of potential therapeutics compounds. Used in conjunction with high-throughput screening, the libraries of stored compounds are often generated for specific purposes as a drug target or disease model. Cheminformatics are commonly used when designing a compound library and software can be used to analyze the screening process.  
BioFocus DPI Launches Compound Library Targeting Protein-Protein Interactions Plus Three New Kinase Libraries