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pravadoline and (3r)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone

pravadoline has been researched along with (3r)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baizman, ER; Beglin, NC; Bell, MR; Casiano, FM; D'Ambra, TE; Eissenstat, MA; Estep, KG; Haycock, DA; Josef, KA; Ward, SJ1
Collantes, ER; Eissenstat, MA; Howlett, AC; Shim, JY; Subramaniam, B; Ward, SJ; Welsh, WJ1
Angus, JA; Christopoulos, A; McRae, K; Moloney, GP; Robertson, AD; Robinson, M; Stoermer, MJ; Wright, CE1

Other Studies

3 other study(ies) available for pravadoline and (3r)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone

ArticleYear
Conformationally restrained analogues of pravadoline: nanomolar potent, enantioselective, (aminoalkyl)indole agonists of the cannabinoid receptor.
    Journal of medicinal chemistry, 1992, Volume: 35, Issue:1

    Topics: Analgesics; Animals; Indoles; Male; Molecular Conformation; Rats; Rats, Inbred Strains; Receptors, Cannabinoid; Receptors, Drug; Structure-Activity Relationship

1992
Three-dimensional quantitative structure-activity relationship study of the cannabimimetic (aminoalkyl)indoles using comparative molecular field analysis.
    Journal of medicinal chemistry, 1998, Nov-05, Volume: 41, Issue:23

    Topics: Animals; Benzoxazines; Binding, Competitive; Brain; Cannabinoids; Cyclohexanols; In Vitro Techniques; Indoles; Models, Molecular; Molecular Conformation; Molecular Mimicry; Morpholines; Naphthalenes; Radioligand Assay; Rats; Receptors, Cannabinoid; Receptors, Drug; Structure-Activity Relationship

1998
Synthesis and cannabinoid activity of 1-substituted-indole-3-oxadiazole derivatives: novel agonists for the CB1 receptor.
    European journal of medicinal chemistry, 2008, Volume: 43, Issue:3

    Topics: Analgesics; Animals; Binding Sites; Cannabinoids; Drug Design; Hydrogen Bonding; Hydrophobic and Hydrophilic Interactions; Indoles; Inhibitory Concentration 50; Mice; Oxadiazoles; Rats; Receptor, Cannabinoid, CB1; Substrate Specificity

2008