Orally Active MMP-1 Sparing α-tetrahydropyranyl and α-piperidinyl Sulfone Matrix Metalloproteinase (MMP) Inhibitors with Efficacy in Cancer, Arthritis, and Cardiovascular Disease

Daniel P Becker, Thomas E. Barta, Louis J. Bedell, Terri L. Boehm

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageAmerican English
JournalChemistry: Faculty Publications and Other Works
Volume53
Issue number18
DOIs
StatePublished - Sep 23 2010

Keywords

  • MMP-1
  • inhibitors
  • cancer
  • arthritis
  • cardiovascular disease

Disciplines

  • Chemistry

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