EPSRC Reference: |
EP/C007247/1 |
Title: |
Development of an efficient approach for the synthesis of LL-Z1640-2 and related resorcyclic lactones. |
Principal Investigator: |
Marquez, Dr R |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
College of Life Sciences |
Organisation: |
University of Dundee |
Scheme: |
First Grant Scheme Pre-FEC |
Starts: |
01 September 2005 |
Ends: |
31 May 2006 |
Value (£): |
111,054
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EPSRC Research Topic Classifications: |
Chemical Synthetic Methodology |
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EPSRC Industrial Sector Classifications: |
Healthcare |
Pharmaceuticals and Biotechnology |
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Related Grants: |
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Panel History: |
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Summary on Grant Application Form |
The powerful compound LL-Z1640-2 was isolated in 1978, and it was originally classified as anti-bacterial agent. However, in the early 1990's major discoveries regarding its biological activities were reported. Some of these new discoveries included new and selective ant-tumour properties (i.e. can target tumours without targeting other biological processes). Interestingly, other compounds closely resembling LL-Z1640-2 have also been recentky isolated and they also seem to have very high potency against cancer processes. Unfortunately, none of these compounds (LL-Z1640-2, hypothemycin, 87-250904-F1, 7-oxo-zeaenol, zeaenol, and radicicol) can be isolated in large enough amounts from their natural sources to make them useful for development as cancer treatment agents.This low natural abundance makes a syntheses of these important compounds imperative if we are to benefit from its biological properties. Thus far, two research groups have developed a way to make LL-Z1640-2 in the laboratory. However, their difficult approach can only produce LL-Z1640-2 in very small amounts, after a long time and at a very high cost.We are proposing to take advantage of the structural similarities between all these compounds to develop a general and flexible way to prodice LL-Z1640-2, hypothemycin, 87-250904-F1, 7-oxo-zeaenol, and zeaenol 5. Our approach will be a faster, cheaper and more efficient way to produce larger amounts of material which would be of invaluable for the determination of their potential as anti-cancer drugs.
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Key Findings |
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Potential use in non-academic contexts |
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Impacts |
Description |
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Summary |
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Date Materialised |
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Sectors submitted by the Researcher |
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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Project URL: |
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Further Information: |
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Organisation Website: |
http://www.dundee.ac.uk |