BioFocus DPI releases five new compound libraries

7 Apr 2008

BioFocus DPI today introduces new FieldFocus and SoftFocus libraries that were created with advanced modeling tools. The libraries consist of novel drug-like compounds specifically targeted towards kinases and voltage-dependent ion channels. These targets represent two of the most important and commonly studied protein classes for drug discovery. Two new lead-like ThemePair Fragment libraries from BioFocus DPI are also being released.

Following the success of the FieldFocus ion channel libraries, BioFocus DPI is introducing its first FieldFocus kinase (FFK) libraries. The FFK01 and FFK02 libraries have been designed using a new in silico, fragment-based approach to tackle kinase library design from a ligand perspective, complementing the highly successful SoftFocus kinase libraries.

BioFocus DPI is also releasing its latest SoftFocus ion channel (SFI) library. SFI08 contains approximately 500 compounds designed to target voltage-dependent ion channels. These libraries were created using BioFocus DPI’s proprietary chemogenomic tool Helical Domain Recognition Analysis, which has been proven to generate potent and selective hit series.

Two new ThemePair Fragment (TPF) libraries are also now available from BioFocus DPI. The TPF10 library contains lead-like compounds substituted with a single heavy atom and are designed for use in X-ray crystallographic screening. The TPF11 library is based on nine bicyclic scaffolds suitable for both conventional bioassays as well as high-throughput affinity screening.

“We are constantly evolving the design tools used in the production of our focused libraries and the latest FieldFocus kinase libraries are an exciting new addition to our portfolio,” said Richard Hill, Director Discovery Products, BioFocus DPI.

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