A New Class of Serine and Cysteine Protease Inhibitor with Chemotherapeutic Potential

Abstract

Metastasis of cancer is dependent on a variety of biologically active compounds including serine proteases. Inhibition of proteases such as plasmin is a potential route for both suppression of metastatic lesions and control of primary tumor growth. Synthesis of tetrahydrothiopyran-4-one based inhibitors of plasmin containing either a diamine or amide/amine side chain was undertaken. Initial attempts to produce the inhibitors through amide alkylation and reductive amination proved futile. The diamine inhibitor was finally produced using amine alkylation chemistry. A monoamine side product of this reaction forms the starting material for the other inhibitor. A simple peptide coupling reaction converts the monoamine to the amide/amine inhibitor. Preliminary testing on the crude products shows both inhibitors to have some activity against plasmin with a Ki of 6 mM for the diamine inhibitor and 3 mM for the amide/amine inhibitor.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 1997
Accession Number
ADA332879

Entities

People

  • Tanya C. Sanders

Organizations

  • Brown University

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Alcohols
  • Amines
  • Blood
  • Blood Vessels
  • Cells
  • Chemistry
  • Chlorides
  • Column Chromatography
  • Cysteine
  • Enzyme Inhibitors
  • Ethers
  • Fibrin Modulating Agents
  • Inhibition
  • Materials
  • Neoplasms
  • Neutral Amino Acids
  • Sulfur Compounds

Fields of Study

  • Chemistry

Readers

  • Molecular and Cellular Biochemistry
  • Oncology (Cancer Research).
  • Organic Chemistry