SELECTION OF SMALL MOLECULE MIMETICS OF ERYTHROPOIETIN

Information

  • Research Project
  • 2867164
  • ApplicationId
    2867164
  • Core Project Number
    R43DK055930
  • Full Project Number
    1R43DK055930-01
  • Serial Number
    55930
  • FOA Number
  • Sub Project Id
  • Project Start Date
    5/1/1999 - 25 years ago
  • Project End Date
    4/30/2000 - 24 years ago
  • Program Officer Name
    BADMAN, DAVID G.
  • Budget Start Date
    5/1/1999 - 25 years ago
  • Budget End Date
    4/30/2000 - 24 years ago
  • Fiscal Year
    1999
  • Support Year
    1
  • Suffix
  • Award Notice Date
    4/19/1999 - 25 years ago

SELECTION OF SMALL MOLECULE MIMETICS OF ERYTHROPOIETIN

The erythropoietin receptor (EPOR) is a transmembrane protein that mediates the transmission of a signal from the hormone erythropoietin (EPO) to a blood cell progenitor; this signal induces the maturation of the cell to an erythrocyte. Like many transmembrane receptor proteins, EPOR transmits the signal across the cell membrane by dimerizing in response to divalent binding by the EPO protein. A small organic molecule that can dimerize EPOR in the absence of EPO would be highly valued as a therapeutic treatment for severely anemic patients. A small-peptide EPOR mimetic has been developed that can dimerize EPOR, although peptide- based drugs suffer from poor bioavailability and rapid breakdown in vivo. A combinatorial chemistry-based drug discovery program has been developed at NeoGenesis which is capable of synthesizing and rapidly screening millions of drug-like molecules to identify small-molecule ligands for any protein target. This project proposes the synthesis of new combinatorial libraries of small organic molecules and the development of novel screening protocols which will identify compounds that dimerize or can be modified to dimerize EPOR. If this strategy is successful, it will be applied to other high-value drug targets which work by similar mechanisms, such as growth hormone and insulin receptors. PROPOSED COMMERCIAL APPLICATIONS: This project will develop a small-molecule mimetic of erythropoietin, and the technology developed here will be applicable to the development of small-molecule mimetics of growth hormone, insulin, and other hormones which function through dimerization of membrane-spanning receptors.

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R43
  • Administering IC
    DK
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
  • Organization Name
    NEOGENESIS DRUG DISCOVERY, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    02139
  • Organization District
    UNITED STATES