N-Methylacetamide Analog of Salvinorin A: A Highly Potent and Selective κ-Opioid Receptor Agonist with Oral Efficacy-Reference-Cited by-同舟云学术

N-Methylacetamide Analog of Salvinorin A: A Highly Potent and Selective κ-Opioid Receptor Agonist with Oral Efficacy

Published:2007-10-19 Issue:1 Volume:324 Page:188-195
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Béguin Cécile,Potter David N.,DiNieri Jennifer A.,Munro Thomas A.,Richards Michele R.,Paine Tracie A.,Berry Loren,Zhao Zhiyang,Roth Bryan L.,Xu Wei,Liu-Chen Lee-Yuan,Carlezon William A.,Cohen Bruce M.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference39 articles.

1. Antinociceptive and Hypothermic Effects of Salvinorin A Are Abolished in a Novel Strain of κ-Opioid Receptor-1 Knockout Mice

2. Novel developments with selective, non-peptidic kappa-opioid receptor agonists

3. Synthesis and in vitro pharmacological evaluation of salvinorin A analogues modified at C(2)

4. Synthesis and in vitro evaluation of salvinorin A analogues: Effect of configuration at C(2) and substitution at C(18)

5. Hallucinatory and rewarding effect of salvinorin A in zebrafish: κ-opioid and CB1-cannabinoid receptor involvement

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