PROTEIN KINASE C MODULATORS FROM MARINE INVERTEBRATES

Information

  • Research Project
  • 2189451
  • ApplicationId
    2189451
  • Core Project Number
    R43GM051133
  • Full Project Number
    1R43GM051133-01
  • Serial Number
    51133
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/1/1994 - 30 years ago
  • Project End Date
    9/30/1994 - 30 years ago
  • Program Officer Name
  • Budget Start Date
    4/1/1994 - 30 years ago
  • Budget End Date
    9/30/1994 - 30 years ago
  • Fiscal Year
    1994
  • Support Year
    1
  • Suffix
  • Award Notice Date
    3/24/1994 - 30 years ago

PROTEIN KINASE C MODULATORS FROM MARINE INVERTEBRATES

Discovery of new drugs depends largely upon random screening directed towards specific enzyme targets. Protein kinase C (PKC), a family of serine/threonine-specific protein kinases, is critical in the control of multiple cellular responses, including gene expression, proliferation, differentiation and tumor promotion, and has thus become a primary target in the development of drug. Despite its enormous therapeutic potential, only a few drug candidates that utilize the PKC pathway have been discovered. Recent advances in molecular biology have paved the way for expression of target isoenzymes of P2KC in insect cells in high yields, which has enabled mass screening of samples. Marine organisms have proven to be a very valuable source of biologically active compounds. However, their potential as a source for new pharmaceuticals is still largely unexplored. The primary goal of the current proposal is to screen extracts derived from marine invertebrates in assays against isoenzymes of protein kinase C. To represent species diversity, the marine organisms are collected from different geographical locations. The long range objectives are to isolate and characterize small organic molecules from these organisms that selectively inhibit or activate protein kinase C isoenzymes and to evaluate their therapeutic potential.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    821
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    MCHA
  • Study Section Name
    Medicinal Chemistry Study Section
  • Organization Name
    SPHINX PHARMACEUTICALS CORPORATION
  • Organization Department
  • Organization DUNS
  • Organization City
    DURHAM
  • Organization State
    NC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    27717
  • Organization District
    UNITED STATES