Biocatalytic Synthesis of Selective D1 Agonists

Information

  • Research Project
  • 6338003
  • ApplicationId
    6338003
  • Core Project Number
    R43DA014174
  • Full Project Number
    1R43DA014174-01
  • Serial Number
    14174
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/2001 - 23 years ago
  • Project End Date
    6/28/2002 - 22 years ago
  • Program Officer Name
    HILLERY, PAUL
  • Budget Start Date
    9/30/2001 - 23 years ago
  • Budget End Date
    6/28/2002 - 22 years ago
  • Fiscal Year
    2001
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/29/2001 - 23 years ago

Biocatalytic Synthesis of Selective D1 Agonists

DESCRIPTION (provided by applicant): "Drug addition is a complex illness. It is characterized by compulsive, at times uncontrollable drug craving, seeking, and use that persist even in the face of extremely negative consequences." As a consequence of the extraordinary personal, social, and health care costs associated with this problem, effective drug abuse treatment has become a national goal. There is preclinical and clinical evidence to suggest that a potent and selective dopamine D1 agonist would provide effective treatment for reducing craving and potentially decreasing the recurrence of cocaine use once a subject ceases using the drug. Currently, there are a number of deficiencies that must be overcome with existing D1 agonist, including poor oral bioavailability, short half-life, lack of selectivity for D1 receptors, and genotoxicity. Despite significant work using conventional chemical synthetic methods, such compounds have not yet been identified. We propose utilizing novel combinatorial biocatalysis technology on known D1 agonists, which for the deficiencies stated above fail to meet the criteria for use in a clinical setting. This technology can rapidly produce unique derivatives of these lead molecules and permit a search of chemical diversity space previously explored by previous efforts. This approach will prepare and rapidly assess numerous compounds with unique substitutions that may culminate in the identification of commercially viable candidates for the treatment of cocaine abuse. PROPOSED COMMERCIAL APPLICATION: The proposed work affords a substantial opportunity for commercial success. The clinical proof of concept experiment in humans (13) indicates a high probability of marketability should a compound be identified that overcomes the current liabilities of known D, agonists (1). Our proposed research focuses on the discovery of a series of derivatives that may have superior water solubility, reduced systemic toxicity, and higher potency and selectivity for the D, receptor. Such compounds can be directly developed for use in the treatment of addiction.

IC Name
NATIONAL INSTITUTE ON DRUG ABUSE
  • Activity
    R43
  • Administering IC
    DA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    192199
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    279
  • Ed Inst. Type
  • Funding ICs
    NIDA:192199\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ALBANY MOLECULAR RESEARCH, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    ALBANY
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    122125098
  • Organization District
    UNITED STATES