Drug discovery: A question of library design.

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Bibliographic Details
Title: Drug discovery: A question of library design.
Authors: Hajduk, Philip J., Galloway, Warren R. J. D., Spring, David R.
Source: Nature. 2/3/2011, Vol. 470 Issue 7332, p42-43. 2p. 1 Color Photograph, 1 Diagram.
Subjects: Drug design, Experimental design, Molecular weights, Bioactive compounds, Experiments
Abstract: The article offers the authors' insights on the benefits and defects of fragment-based screening (FBS) and diversity-oriented synthesis (DOS) methods in creating libraries of compounds for drug discovery. It says that FBS design offers varied libraries and improved use of synthetic resources. It tells that DOS libraries develop diverse molecules whose molecular weights are proximate to the masses of drug-like compounds. It adds that unlike DOS, FBS would not offer non-traditional target hints.
Database: Psychology and Behavioral Sciences Collection
Description
Abstract:The article offers the authors' insights on the benefits and defects of fragment-based screening (FBS) and diversity-oriented synthesis (DOS) methods in creating libraries of compounds for drug discovery. It says that FBS design offers varied libraries and improved use of synthetic resources. It tells that DOS libraries develop diverse molecules whose molecular weights are proximate to the masses of drug-like compounds. It adds that unlike DOS, FBS would not offer non-traditional target hints.
ISSN:00280836
DOI:10.1038/470042a