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Summary
September 2004, Vol. 13, No. 9, Pages 1149-1157
, DOI 10.1517/13543784.13.9.1149
Exploitation of silicon medicinal chemistry in drug discoveryJohn S MillsAmedis Pharmaceuticals Ltd, 162 Cambridge Science Park, Milton Road, Cambridge, CB4 0GP, UK. john.mills@amedis-pharma.com There remains considerable pressure on the pharmaceutical industry to increase productivity and reduce the attrition of drug candidates. Genomics, parallel chemistry and high-throughput biology have not yielded the anticipated benefits, resulting in a renewed focus on validated targets and an aim to generate drugs directed towards such targets, which have a clear advantage. One strategy to identify and develop best-in-class drugs is to apply a high degree of innovation in chemistry and apply this to targets from gene families that have been clinically validated as tractable and drugable. The application of organosilicon medicinal chemistry in the context of privileged structures to aid drug design and development is one such innovative approach that is reviewed in this paper. Forward Links to Citing ArticlesW. Peter Lippert, Christian Burschka, Kathrin Götz, Martin Kaupp, Diana Ivanova, Claudine Gaudon, Yoshiteru Sato, Pierre Antony, Natacha Rochel, Dino Moras, Hinrich Gronemeyer, Reinhold Tacke. (2009) Silicon Analogues of the RXR-Selective Retinoid Agonist SR11237 (BMS649): Chemistry and Biology. ChemMedChem 4:7, 1143-1152 Online publication date: 6-Aug-2009. CrossRef Henrik Ottosson, Patrick G. Steel. (2006) Silylenes, Silenes, and Disilenes: Novel Silicon-Based Reagents for Organic Synthesis?. Chemistry - A European Journal 12:6, 1576 CrossRef |
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