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Novel bisphosphonate inhibitors of the human farnesyl pyrophosphate synthase
Joris W De Schutter1, Serge Zaretsky, Sarah Welbourn
1Department of Chemistry, McGill University, Montreal, Quebec, Canada.
Abstract:
A structure-based approach was pursued in designing novel bisphosphonate inhibitors of the human farnesyl pyrophosphate synthase (hFPPS). Preliminary SAR and structural evidence for the simultaneous binding of these inhibitors into the isopentenyl pyrophosphate (IPP) and the geranyl pyrophosphate (GPP) substrate sub-pockets of the enzyme are presented.
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