Publication | Open Access
Orally Active MMP-1 Sparing α-Tetrahydropyranyl and α-Piperidinyl Sulfone Matrix Metalloproteinase (MMP) Inhibitors with Efficacy in Cancer, Arthritis, and Cardiovascular Disease
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Citations
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References
2010
Year
Spare Mmp-1PharmacotherapyPharmaceutical ChemistryInflammatory ArthritisTumor BiologyMedicinal ChemistryAnti-cancer AgentRadiation OncologyMolecular OncologyCancer ResearchRheumatologyBovine Cartilage DegradationTumor GrowthCancer TreatmentDrug DevelopmentPharmacologyAnti-inflammatoryCardiovascular DiseaseMedicineDrug Discovery
α-Sulfone-α-piperidine and α-tetrahydropyranyl hydroxamates were explored that are potent inhibitors of MMP's-2, -9, and -13 that spare MMP-1, with oral efficacy in inhibiting tumor growth in mice and left-ventricular hypertrophy in rats and in the bovine cartilage degradation ex vivo explant system. α-Piperidine 19v (SC-78080/SD-2590) was selected for development toward the initial indication of cancer, while α-piperidine and α-tetrahydropyranyl hydroxamates 19w (SC-77964) and 9i (SC-77774), respectively, were identified as backup compounds.
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