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Content archived on 2024-05-27

Design and development of novel inhibitor compounds of hepatitis c ires (internal ribosome entry site ) function

Objective

HVC is a growing European medical problem here there is no effective long-term therapy. Mostly fatal, this infectious disease may be chronically carried by 5 million Europeans placing a huge burden on medical services and resources. Novel and effective antiviral therapies are therefore urgently needed. We use rational drug design to develop new drugs to combat HCV at a critical stage in its life cycle. Our dugs fit a specific target in the RNA structure, freezing its shape, it is no longer able to bind its native protein, and thus viral replication is inhibited. We will determine the 3D structure of the RNA target, design and make novel drugs, develop assays to measure inhibition of RNA function, and make through iterative cycles lead molecules. In collaboration withal pharmaceutical partner such drugs would be entered into a clinical evaluation programme. This research will benefit Europeans by producing novel therapies to this debilitating and often fatal disease.

Fields of science (EuroSciVoc)

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Call for proposal

Data not available

Coordinator

VERNALIS (CAMBRIDG) LIMITED
EU contribution
No data
Address
Granta Park, Abington
CB1 6GB CAMBRIDGE
United Kingdom

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Total cost
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Participants (4)