Summary
September 2004, Vol. 13, No. 9, Pages 1149-1157 , DOI 10.1517/13543784.13.9.1149

Exploitation of silicon medicinal chemistry in drug discovery

John S Mills, Graham A Showell
Amedis 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.

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Forward Links to Citing Articles

W. 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
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Authors:
John S Mills
Graham A Showell
Keywords:
drug discovery
privileged structure
silicon