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      Highly selective fluorescent analogue of the potent delta-opioid receptor antagonist Dmt-Tic.

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          Abstract

          A fluorescent tripeptide probe derived by coupling fluorescein to H-Dmt-Tic-Glu-NH2 was developed to interact with delta-opioid receptors with high affinity (Ki = 0.035 nM) and selectivity (Ki(mu)/Ki(delta) = 4371). It acts as an irreversible delta-opioid receptor antagonist, and binding to NG108-15 cells is blocked by the standard nonpeptidic delta-opioid receptor antagonist naltrindole. This probe should prove useful in the study of the distribution of delta-opioid receptors in tissues and the internalization of opioid peptides during signal transduction.

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          Author and article information

          Journal
          J Med Chem
          Journal of medicinal chemistry
          American Chemical Society (ACS)
          0022-2623
          0022-2623
          Dec 16 2004
          : 47
          : 26
          Affiliations
          [1 ] Department of Toxicology, University of Cagliary, I-09126, Cagliary, Italy.
          Article
          10.1021/jm040128h
          15588089
          52c0453f-ccad-470f-a34c-4aaa6ec83f59
          History

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