Aspirin-like molecules that covalently inactivate cyclooxygenase-2

Science. 1998 May 22;280(5367):1268-70. doi: 10.1126/science.280.5367.1268.

Abstract

Many of aspirin's therapeutic effects arise from its acetylation of cyclooxygenase-2 (COX-2), whereas its antithrombotic and ulcerogenic effects result from its acetylation of COX-1. Here, aspirin-like molecules were designed that preferentially acetylate and irreversibly inactivate COX-2. The most potent of these compounds was o-(acetoxyphenyl)hept-2-ynyl sulfide (APHS). Relative to aspirin, APHS was 60 times as reactive against COX-2 and 100 times as selective for its inhibition; it also inhibited COX-2 in cultured macrophages and colon cancer cells and in the rat air pouch in vivo. Such compounds may lead to the development of aspirin-like drugs for the treatment or prevention of immunological and proliferative diseases without gastrointestinal or hematologic side effects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylation
  • Acetylene / analogs & derivatives*
  • Acetylene / chemical synthesis
  • Acetylene / chemistry
  • Acetylene / pharmacology
  • Alkynes
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis*
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Aspirin / chemistry
  • Aspirin / pharmacology
  • Binding Sites
  • Cell Division / drug effects
  • Cell Line
  • Colonic Neoplasms / enzymology
  • Colonic Neoplasms / pathology
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / chemical synthesis*
  • Cyclooxygenase Inhibitors / chemistry
  • Cyclooxygenase Inhibitors / pharmacology
  • Dinoprostone / biosynthesis
  • Drug Design
  • Humans
  • Indomethacin / pharmacology
  • Isoenzymes / chemistry
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Macrophages / enzymology
  • Membrane Proteins
  • Mutagenesis, Site-Directed
  • Prostaglandin D2 / biosynthesis
  • Prostaglandin-Endoperoxide Synthases / chemistry
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Rats
  • Rats, Inbred Lew
  • Sulfides / chemical synthesis*
  • Sulfides / chemistry
  • Sulfides / pharmacology
  • Thromboxane B2 / biosynthesis
  • Tumor Cells, Cultured

Substances

  • Alkynes
  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Membrane Proteins
  • Sulfides
  • o-(acetoxyphenyl)hept-2-ynyl sulfide
  • Thromboxane B2
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Dinoprostone
  • Acetylene
  • Aspirin
  • Prostaglandin D2
  • Indomethacin