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  Natural products as potential antitumour and antimicrobial agents – synthesis and biological studies (SEARCEYU17SF)


   School of Pharmacy

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  Prof M Searcey  No more applications being accepted

About the Project

Compounds that come from nature have formed the backbone of cancer treatment for many years. Probably most well known is paclitaxel, with the trade name Taxol, which is used in the treatment of breast and ovarian cancers. Others, such as vincristine and vinblastine from the Periwinkle plant, have an even longer history of clinical use. Doxorubicin is a well-known, clinically anticancer natural product that exerts its effects through inhibition of an enzyme called topoisomerase II and although well used in the clinic, it has several side effects that limit its utility. We are interested in the biological activity of a family of natural products called simocyclinones (ref i-iii), some of which inhibit topoisomerases and have potential both as antitumour and antimicrobial agents. In this PhD project, we will synthesise analogues of the simocyclinones and study their biological activity, with a view towards generating molecules with better pharmacological properties (see, for example, ref iv). The PhD project will involve synthetic organic chemistry, biosynthesis studies and also some biological assessment and would suit applicants who want to work at the chemistry/biology interface.

The project may be available at an earlier start date of 1 April or 1 July 2017 but should be discussed with the primary supervisor in the first instance.


Funding Notes

This PhD project is offered on a self-funding basis. It is open to applicants with funding or those applying to funding sources. Details of tuition fees can be found at http://www.uea.ac.uk/pgresearch/pgrfees.

A bench fee is also payable on top of the tuition fee to cover specialist equipment or laboratory costs required for the research. The amount charged annually will vary considerably depending on the nature of the project and applicants should contact the primary supervisor for further information about the fee associated with the project.

References

i) Schimana, J et al J. Antibiot. 2000, 53, 779-787

ii) Schimana, J.; Walker, M.; Zeeck, A.; Fiedler, H. P. J. Ind. Microbiol. Biotechnol. 2001, 27, 144-148

iii) Flatman, R. H.; Howells, A. J.; Heide, L.; Fiedler, H. P.; Maxwell, A. Antimicrob. Agents Chemother. 2005, 49, 1093-1100

iv) Austin, M. J.; Hearnshaw, S. J.; Mitchenall, L. A.; McDermott, P. J.; Howell, L. A.; Searcey M. MedChemComm 2016 doi 10.1039/C6MD))229C

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