Zobrazeno 1 - 5
of 5
pro vyhledávání: '"C. M. Dimeglio"'
Publikováno v:
Journal of Medicinal Chemistry. 41:167-174
Among the nonclassical cannabinoids, CP-55,244 (4), which incorporates an axial 14 beta-hydroxymethyl group, is pharmacologically 30 times more potent than its prototype CP-47,497 (2) and 300 times more potent than delta 9-THC (1). It has a high degr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d74bfb0a7e32c159885b32d96967a876
https://doi.org/10.1021/jm960410r
https://doi.org/10.1021/jm960410r
Autor:
T. J. Alavosus, J. H. Brown, Dwight A. Sweigart, C. M. Dimeglio, W. H. Hallows, C. H. Bushweller, Robert D. Pike, N. S. Lennhoff, W. J. Ryan
Publikováno v:
Organometallics. 11:2841-2854
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3ab14f4e5fd3860312eaf85476bb93a
https://doi.org/10.1021/om00044a026
https://doi.org/10.1021/om00044a026
Publikováno v:
Pharmaceutical research. 10(8)
The solution conformations of the opioid phenylmorphan (5-m-hydroxyphenyl-2-methylmorphan) and its 9 alpha-methyl analogue were studied using one- and two-dimensional high resolution NMR techniques. The NMR spectra were analyzed by interpreting the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2ca622f1f65be422753da608ec5cf42
https://pubmed.ncbi.nlm.nih.gov/8415408
https://pubmed.ncbi.nlm.nih.gov/8415408
Publikováno v:
Molecular pharmacology. 43(1)
The interactions of several hallucinogenic phenethylamines with the biologically relevant electron acceptor imidazolium chloride have been investigated by monitoring phenethylamine 1H NMR chemical shift changes upon complex formation. Methoxy- and me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::527a9404c0b4877c1913cd3985e95bed
https://pubmed.ncbi.nlm.nih.gov/8423771
https://pubmed.ncbi.nlm.nih.gov/8423771
Publikováno v:
Journal of medicinal chemistry. 34(5)
A series of structurally related pregnane analogues which exhibit a wide range of anesthetic potencies were incorporated into unilamellar egg lecithin vesicles and their relative mobilities examined with 1H and 2H high-resolution NMR spectroscopy. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0d8731c8fcd71c92d099d10ccd8cdec0
https://pubmed.ncbi.nlm.nih.gov/2033593
https://pubmed.ncbi.nlm.nih.gov/2033593