EconPapers    
Economics at your fingertips  
 

A question of library design

Philip J. Hajduk, Warren R. J. D. Galloway and David R. Spring
Additional contact information
Philip J. Hajduk: Abbott Laboratories, Abbott Park, Illinois 60064, USA. philip.hajduk@abbott.com
Warren R. J. D. Galloway: University of Cambridge, Cambridge CB2 1EW, UK. spring@ch.cam.ac.uk
David R. Spring: University of Cambridge, Cambridge CB2 1EW, UK. spring@ch.cam.ac.uk

Nature, 2011, vol. 470, issue 7332, 42-43

Abstract: Two approaches have emerged for creating libraries of compounds for use in biological screening assays for drug discovery — fragment-based ligand design and diversity-oriented synthesis. Advocates of each approach discuss their favoured strategy.

Date: 2011
References: Add references at CitEc
Citations: View citations in EconPapers (1)

Downloads: (external link)
https://www.nature.com/articles/470042a Abstract (text/html)
Access to the full text of the articles in this series is restricted.

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:470:y:2011:i:7332:d:10.1038_470042a

Ordering information: This journal article can be ordered from
https://www.nature.com/

DOI: 10.1038/470042a

Access Statistics for this article

Nature is currently edited by Magdalena Skipper

More articles in Nature from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().

 
Page updated 2025-03-19
Handle: RePEc:nat:nature:v:470:y:2011:i:7332:d:10.1038_470042a