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Details of Grant 

EPSRC Reference: GR/S19929/01
Title: Synthesis of Bioactive Marine Macrolides: Peloruside A and Reidispongiolide A
Principal Investigator: Paterson, Professor I
Other Investigators:
Researcher Co-Investigators:
Project Partners:
Department: Chemistry
Organisation: University of Cambridge
Scheme: Standard Research (Pre-FEC)
Starts: 01 May 2003 Ends: 31 October 2006 Value (£): 246,498
EPSRC Research Topic Classifications:
Biological & Medicinal Chem. Chemical Synthetic Methodology
EPSRC Industrial Sector Classifications:
Chemicals Healthcare
Pharmaceuticals and Biotechnology No relevance to Underpinning Sectors
Related Grants:
Panel History:  
Summary on Grant Application Form
Peloruside A, isolated from a New Zealand sponge, is a potent inhibitor of cell proliferation at the nanomolar level, causing cell cycle arrest at the G2/M phase, and inducing apoptosis. By sharing the same microtubule-stabilising mechanism as the clinically important anticancer drug, Taxol, peloruside A joins an elite group of natural products (including discodermolide, the epothilones, eleuthorobin and laulimalide) as potential chemotherapeutic agents for the treatment of solid tumours (such as breast, ovarian and colorectal cancers). Reidispongiolide A, isolated from a New Caledonian sponge, is a potent antimicrofilament agent and is active against (P-glycoprotein-mediated) multi-drug resistant cancer cells. By exploiting novel methods of substrate and reagent based stereocontrol, this research programme will focus on developing a flexible synthesis of the 16-membered macrolide, peloruside A, along with conducting studies towards the synthesis of the 26-membered macrolide, reidispongiolide A, in order to establish their absolute configurations and to enable further preclinical biological evaluation.
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Organisation Website: http://www.cam.ac.uk