Journal of Medicinal Chemistry · 2009 · 104 citations · 12 references
PharmacyMedicinal ChemistryPharmacologyBone MetabolismDrug DesignDrug DiscoveryBone TissueEnzyme InhibitionHit-to-lead OptimizationLead Compound DesignBone Matrix BiochemistryHigh-throughput Screening AssaysMineralization InhibitorsSmall Molecule Drug DesignSmall Molecule Drug DevelopmentSmall-molecule Library ConstructionSmall-molecule Library DesignSubcutaneous Drug Administration
We report the characterization and optimization of drug-like small molecule inhibitors of tissue-nonspecific alkaline phosphatase (TNAP), an enzyme critical for the regulation of extracellular matrix calcification during bone formation and growth. High-throughput screening (HTS) of a small molecule library led to the identification of arylsulfonamides as potent and selective inhibitors of TNAP. Critical structural requirements for activity were determined, and the compounds were subsequently profiled for in vitro activity and bioavailability parameters including metabolic stability and permeability. The plasma levels following subcutaneous administration of a member of the lead series in rat was determined, demonstrating the potential of these TNAP inhibitors as systemically active therapeutic agents to target various diseases involving soft tissue calcification. A representative member of the series was also characterized in mechanistic and kinetic studies.
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Lovisa Hessle, H. Clarke Anderson, Sonoko Narisawa et al. · Proceedings of the National Academy of Sciences · 2002 · 859 citations · Full text
William N. Addison, Fereshteh Azari, Esben S. Sørensen et al. · Journal of Biological Chemistry · 2007 · 401 citations · Full text