sr141716 has been researched along with jte 907 in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brogi, S; Corelli, F; Di Marzo, V; Ligresti, A; Mugnaini, C; Pasquini, S; Tafi, A | 1 |
| Alauddin, MM; Gelovani, JG; Ivanov, RA; Rabinovich, B; Shavrin, A; Turkman, N; Volgin, A | 1 |
| Chen, JZ; Han, S; Xie, X; Zhang, FF | 1 |
3 other study(ies) available for sr141716 and jte 907
| Article | Year |
|---|---|
Three-dimensional quantitative structure-selectivity relationships analysis guided rational design of a highly selective ligand for the cannabinoid receptor 2.
Topics: Computer Simulation; Drug Design; Humans; Ligands; Models, Molecular; Molecular Structure; Quantitative Structure-Activity Relationship; Quinolones; Receptor, Cannabinoid, CB1; Receptor, Cannabinoid, CB2; Recombinant Proteins; Stereoisomerism | 2011 |
Fluorinated cannabinoid CB2 receptor ligands: synthesis and in vitro binding characteristics of 2-oxoquinoline derivatives.
Topics: Binding, Competitive; Cell Line, Tumor; Dose-Response Relationship, Drug; Glioma; Humans; Ligands; Molecular Structure; Quinolones; Receptor, Cannabinoid, CB1; Receptor, Cannabinoid, CB2; Stereoisomerism; Structure-Activity Relationship | 2011 |
Design, synthesis, biological evaluation, and comparative docking study of 1,2,4-triazolones as CB1 receptor selective antagonists.
Topics: Amino Acid Sequence; Humans; Magnetic Resonance Spectroscopy; Molecular Docking Simulation; Molecular Sequence Data; Receptor, Cannabinoid, CB1; Sequence Homology, Amino Acid; Spectrometry, Mass, Electrospray Ionization; Triazoles | 2014 |