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

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

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bergeron, C; Bolton, JL; Budzinski, JW; Dietz, BM; Foster, BC; Gafner, S; Glinski, JA; McCollom, MM; McPhail, KL; Rhyu, MR; Russell, FE; Scott, IM	1
Carmody, LC; Dandapani, S; Donckele, E; Feng, Y; Fernandez, C; Germain, AR; Gupta, PB; Lander, ES; Morgan, B; Munoz, B; Nag, PP; Palmer, M; Perez, JR; Schreiber, SL; Verplank, L	1
Cheng, J; McCorvy, JD; Tan, L; Yan, W	1

Reviews

1 review(s) available for (3r)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone and phenylisopropyladenosine

Article	Year
Biased Ligands of G Protein-Coupled Receptors (GPCRs): Structure-Functional Selectivity Relationships (SFSRs) and Therapeutic Potential. Journal of medicinal chemistry, 2018, 11-21, Volume: 61, Issue:22 Topics: Animals; Drug Discovery; Humans; Ligands; Receptors, G-Protein-Coupled; Signal Transduction; Structure-Activity Relationship	2018

Other Studies

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

Article	Year
Alkaloids from Eschscholzia californica and their capacity to inhibit binding of [3H]8-Hydroxy-2-(di-N-propylamino)tetralin to 5-HT1A receptors in Vitro. Journal of natural products, 2006, Volume: 69, Issue:3 Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Alkaloids; Benzylisoquinolines; Dioxoles; Eschscholzia; Humans; Molecular Structure; Receptor, Serotonin, 5-HT1A; Serotonin Receptor Agonists	2006
Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells. Bioorganic & medicinal chemistry letters, 2013, Mar-15, Volume: 23, Issue:6 Topics: Amides; Breast Neoplasms; Cell Line, Tumor; Drug Screening Assays, Antitumor; Female; Humans; Neoplastic Stem Cells; Small Molecule Libraries; Structure-Activity Relationship	2013

Article

Year

Alkaloids from Eschscholzia californica and their capacity to inhibit binding of [3H]8-Hydroxy-2-(di-N-propylamino)tetralin to 5-HT1A receptors in Vitro.

Journal of natural products, 2006, Volume: 69, Issue:3

Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Alkaloids; Benzylisoquinolines; Dioxoles; Eschscholzia; Humans; Molecular Structure; Receptor, Serotonin, 5-HT1A; Serotonin Receptor Agonists

2006

Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells.

Bioorganic & medicinal chemistry letters, 2013, Mar-15, Volume: 23, Issue:6

Topics: Amides; Breast Neoplasms; Cell Line, Tumor; Drug Screening Assays, Antitumor; Female; Humans; Neoplastic Stem Cells; Small Molecule Libraries; Structure-Activity Relationship

2013