Selective antagonism by naloxonazine of antinociception by Tyr-d-Arg-Phe-β-Ala, a novel dermorphin analogue with high affinity at μ-opioid receptors-Reference-Cited by-同舟云学术

Selective antagonism by naloxonazine of antinociception by Tyr-d-Arg-Phe-β-Ala, a novel dermorphin analogue with high affinity at μ-opioid receptors

Published:2000-04 Issue:2 Volume:395 Page:107-112
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Sakurada Shinobu,Takeda Satoshi,Sato Takumi,Hayashi Takafumi,Yuki Masayuki,Kutsuwa Motoharu,Tan-No Koichi,Sakurada Chikai,Kisara Kensuke,Sakurada Tsukasa

Publisher

Elsevier BV

Subject

Pharmacology

Reference27 articles.

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3. N-terminal tetrapeptide of dermorphin and d-Arg-substituted tetrapeptides: inactivation process of the antinociceptive activity by peptidase;Chaki;Life Sci.,1990

4. Comparison of the antinociceptive effects of new [d-Arg2]-dermorphin tetrapeptide analogs and morphine in mice;Chaki;Pharmacol. Biochem. Behav.,1988

5. A method for determining loss of pain sensation;D'Amour;J. Pharmacol. Exp. Ther.,1941

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