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Research ArticleArticle

A Cytochrome P450-Derived Epoxygenated Metabolite of Anandamide Is a Potent Cannabinoid Receptor 2-Selective Agonist

Natasha T. Snider, James A. Nast, Laura A. Tesmer and Paul F. Hollenberg
Molecular Pharmacology April 2009, 75 (4) 965-972; DOI: https://doi.org/10.1124/mol.108.053439

Article Information

vol. 75 no. 4 965-972
DOI 
https://doi.org/10.1124/mol.108.053439
PubMed 
19171674
Published By 
American Society for Pharmacology and Experimental Therapeutics
Print ISSN 
0026-895X
Online ISSN 
1521-0111
History 
  • Received November 13, 2008
  • Accepted January 26, 2009
  • Published online March 18, 2009.

Article Versions

Copyright & Usage 
The American Society for Pharmacology and Experimental Therapeutics

Author Information

  1. Natasha T. Snider,
  2. James A. Nast,
  3. Laura A. Tesmer and
  4. Paul F. Hollenberg
  1. Department of Pharmacology (N.T.S., J.A.N., P.F.H.) and Division of Rheumatology, Department of Internal Medicine (L.A.T.), University of Michigan Medical School, Ann Arbor, Michigan
  1. Address correspondence to:
    Dr. Paul F. Hollenberg, Department of Pharmacology, The University of Michigan, 2301 MSRB III, 1150 West Medical Center Dr., Ann Arbor, Michigan 48109-5632. E-mail: phollen{at}umich.edu
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Research ArticleArticle

A Cytochrome P450-Derived Epoxygenated Metabolite of Anandamide Is a Potent Cannabinoid Receptor 2-Selective Agonist

Natasha T. Snider, James A. Nast, Laura A. Tesmer and Paul F. Hollenberg
Molecular Pharmacology April 1, 2009, 75 (4) 965-972; DOI: https://doi.org/10.1124/mol.108.053439
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