Guest Open Access Plus | Free Content | About | Sign in | New Users: Sign up | Mark List  

Combinatorial Chemistry & High Throughput Screening

Volume 14 Issue 6
ISSN: 1386-2073
eISSN: 1875-5402

 

   All Titles

  The Design and Application of Target-Focused Compound Libraries
  pp.521-531 (11) Authors: C. John Harris, Richard D. Hill, David W. Sheppard, Martin J. Slater, Pieter F.W. Stouten
 
 
      Abstract

Target-focused compound libraries are collections of compounds which are designed to interact with an individual protein target or, frequently, a family of related targets (such as kinases, voltage-gated ion channels, serine/cysteine proteases). They are used for screening against therapeutic targets in order to find hit compounds that might be further developed into drugs. The design of such libraries generally utilizes structural information about the target or family of interest. In the absence of such structural information, a chemogenomic model that incorporates sequence and mutagenesis data to predict the properties of the binding site can be employed. A third option, usually pursued when no structural data are available, utilizes knowledge of the ligands of the target from which focused libraries can be developed via scaffold hopping. Consequently, the methods used for the design of target-focused libraries vary according to the quantity and quality of structural or ligand data that is available for each target family. This article describes examples of each of these design approaches and illustrates them with case studies, which highlight some of the issues and successes observed when screening target-focused libraries.

 
  Keywords: Library design, target focus, kinase, ion channel, GPCR, PPI, HTS, hit rate, BioFocus, Galapagos, SoftFocus
  Affiliation: BioFocus, Chesterford Research Park, CB10 1XL, UK.
 
  Key: New Content Free Content Open Access Plus Subscribed Content

Bentham Science Publishers
www.benthamscience.com

 

  Copyright © 1994 - 2014   Bentham Science Publishers