Conformational analogies of morphine agonists and antagonists as revealed by carbon-13 NMR spectroscopy
- 1 April 1984
- journal article
- research article
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 22 (4), 258-262
- https://doi.org/10.1002/mrc.1270220413
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- N-methylnalorphine: definition of N-allyl conformation for antagonism at the opiate receptorJournal of Medicinal Chemistry, 1982
- Common anionic receptor site hypothesis: its relevance to the antagonist action of naloxoneJournal of Medicinal Chemistry, 1982
- A comparison of solution, solid state and theoretical conformations of morphineBiochemical and Biophysical Research Communications, 1981
- Conformational analysis. 39. Carbon-13 NMR spectra of saturated heterocycles. 9. Piperidine and N-methylpiperidineJournal of the American Chemical Society, 1980
- New Opiate-Receptor ModelJournal of Pharmaceutical Sciences, 1978
- The opiate receptor: a model explaining structure-activity relationships of opiate agonists and antagonists.Proceedings of the National Academy of Sciences, 1976
- Carbon-13 nuclear magnetic resonance spectra of morphine alkaloidsThe Journal of Organic Chemistry, 1976
- Polyphenolic acids of Lithospermum ruderale. II. Carbon-13 nuclear magnetic resonance of lithospermic and rosmarinic acidsThe Journal of Organic Chemistry, 1976
- Properties of Opiate-Receptor Binding in Rat BrainProceedings of the National Academy of Sciences, 1973
- Nuclear magnetic resonance studies of proton exchange rate, nitrogen inversion rate, and relative size of methyl groups and -NH+ protons in N,N'-dimethylpiperazine hydrochloridesJournal of the American Chemical Society, 1968