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Current Medicinal Chemistry

Volume 17 Issue 19
ISSN: 0929-8673
eISSN: 1875-533X

 

   All Titles

  Statistical Molecular Design of Balanced Compound Libraries for QSAR Modeling
  pp.2001-2016 (16) Authors: A. Linusson, M. Elofsson, I.E. Andersson, M.K. Dahlgren
 
 
      Abstract

A fundamental step in preclinical drug development is the computation of quantitative structure-activity relationship (QSAR) models, i.e. models that link chemical features of compounds with activities towards a target macromolecule associated with the initiation or progression of a disease. QSAR models are computed by combining information on the physicochemical and structural features of a library of congeneric compounds, typically assembled from two or more building blocks, and biological data from one or more in vitro assays. Since the models provide information on features affecting the compounds' biological activity they can be used as guides for further optimization. However, in order for a QSAR model to be relevant to the targeted disease, and drug development in general, the compound library used must contain molecules with balanced variation of the features spanning the chemical space believed to be important for interaction with the biological target. In addition, the assays used must be robust and deliver high quality data that are directly related to the function of the biological target and the associated disease state. In this review, we discuss and exemplify the concept of statistical molecular design (SMD) in the selection of building blocks and final synthetic targets (i.e. compounds to synthesize) to generate information-rich, balanced libraries for biological testing and computation of QSAR models.

 
  Keywords: Statistical molecular design, quantitative structure-activity relationship, factorial design, D-optimal design, Principal Component Analysis, library design, drug design, parallel synthesis
  Affiliation: Umea University, Linnaeus vag 10, SE-901 87, Umea, Sweden.
 
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