TC152

Turning small potent antimycobacterial cyclo(depsi)peptides into drug-like scaffolds

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Principal Investigator (PI)

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Project location

the sponsor

Home Institution

Martin Luther University Halle-Wittenberg

foundation funding

Foundation funding

The Foundation is providing £154,794 in support.

Open Labs Fellow/s

Dr Katja Laqua - Mr Henok Asfaw

GSK’s contribution

GSK allocated in-kind contributions to the project, including scientific expertise in M.tuberculosis in vitro and in vivo assays, medicinal chemistry, DMPK and further profiling activities. GSK will provide access to the relevant facilities as well as the necessary laboratory supplies to carry out the different work packages.

Project Description

Although the Millennium Development Goal to halt and reverse the TB epidemic by 2015 has been achieved, the global burden of TB remains enormous. In 2012, there were 8.6M new cases of TB and 1.3M deaths. Additionally, MDR-TB cases were reported in all the countries surveyed by WHO. According to their estimates, there were roughly 500,000 new MDR-TB cases that year. As of March 2013, 84 countries had reported at least one XDR-TB case. Outcomes for these patients are depressingly poor.

Small peptides, cyclopeptides and cyclodepsipeptides have recently come to the forefront as potential antimycobacterial drug substances. At the Open Lab, Katja and Henok will be focused on the optimization of cyclodepsipeptides and related analogues that have shown good growth inhibitory against TB and no cytotoxicity, in order to turn active compounds of the peptide-type into drug-like molecules by means of combining activity and stability with suitable solubility and membrane permeability properties.

The duration of the project is 24 months and will involve a close collaboration between Martin Luther University Halle and GSK’s Medicines Development Campus at Tres Cantos.