Chapter 12: Unleashing the Power of Semi-Synthesis: The Discovery of Torisel® Check Access
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Published:30 Jul 2014
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Series: Drug Discovery Series
J. S. Skotnicki and M. A. Abou-Gharbia, in Orphan Drugs and Rare Diseases, ed. D. C. Pryde and M. Palmer, The Royal Society of Chemistry, 2014, ch. 12, pp. 347-366.
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Natural products offer unique and creative opportunities for drug discovery. With their complex architecture and multi-faceted functionality, these secondary metabolites often display exquisite pharmacological profiles and properties. Accordingly, natural products provide versatile and innovative starting points to apply the tenets of medicinal chemistry. Rapamycin (Rapamune®) is a potent, polyketide immunosuppressive agent, produced by Streptomyces hygroscopicus. Rapamycin forms a complex with FKBP and mTOR that elicits its unique mechanism of action, central in a number of biological processes. It is approved for the treatment of transplantation rejection. As part of a programme aimed at the identification of novel rapamycin analogues, we have explored systematic semi-synthetic point modifications to functional groups at essential regions of the molecule. The medicinal chemistry design rationale and strategy is highlighted, culminating in the discovery of CCI-779 (temsirolimus, Torisel®). Torisel® was approved (USA, May 2007) for the treatment of advanced renal cell carcinoma.