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Drug Development

Studies from University of Cambridge update current data on drug development

Published in TB and Outbreaks Week, February 2nd, 2010

"A new strategy that combines the concepts of fragment-based drug design and dynamic combinatorial chemistry (DCC) for targeting adenosine recognition sites on enzymes is reported. We demonstrate the use of 5'-deoxy-5'-thioadenosine as a noncovalent anchor fragment in dynamic combinatorial libraries templated by Mycobacterium tuberculosis pantothenate synthetase," scientists writing in the journal Chembiochem report.

"A benzyl disulfide derivative was identified upon library analysis by HPLC. Structural and binding studies of protein-ligand complexes by X-ray crystallography and isothermaltitration calorimetry informed the subsequent optimisation of the DCC hit...

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