Derivatives of β-casomorphins with high analgesic potency
- 1 May 1984
- Vol. 5 (3), 463-470
- https://doi.org/10.1016/0196-9781(84)90070-6
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Participation of both ‘enkephalinase’ and aminopeptidase activities in the metabolism of endogenous enkephalinsNeuroscience, 1983
- Antinociceptive potencies of β-casomorphin analogs as compared to their affinities towards μ and δ opiate receptor sites in brain and peripheryPeptides, 1982
- Naloxazone, a novel opiate antagonist: Irreversible blockade of rat brain opiate receptorsin vitroCellular and Molecular Neurobiology, 1982
- Analgesic activity of intracerebroventricular administration of morphiceptin and β-casomorphins: Correlation with the morphine (μ) receptor binding affinityLife Sciences, 1982
- Evidence for analgesic activity of β-casomorphin in ratsNeuroscience Letters, 1981
- Naloxazone irreversibly inhibits the high affinity binding of [125I]D-ala2-D-leu5-enkephalinLife Sciences, 1981
- Morphiceptin (NH 4 -Tyr-Pro-Phe-Pro-COHN 2 ): a Potent and Specific Agonist for Morphine (μ) ReceptorsScience, 1981
- Opioid activities of β-casomorphinsLife Sciences, 1981
- A superactive antinociceptive pentapeptide, (D‐Met2,Pro5)‐enkephalinamideFEBS Letters, 1977
- The effects of adrenaline, noradrenaline and isoprenaline on inhibitory α‐ and β‐adrenoceptors in the longitudinal muscle of the guinea‐pig ileumBritish Journal of Pharmacology, 1970