1-(4-ethynylphenyl)-4-propyl-2,6,7-trioxabicyclo(2.2.2)octane has been researched along with oleylamide in 1 studies
| Studies (1-(4-ethynylphenyl)-4-propyl-2,6,7-trioxabicyclo(2.2.2)octane) | Trials (1-(4-ethynylphenyl)-4-propyl-2,6,7-trioxabicyclo(2.2.2)octane) | Recent Studies (post-2010) (1-(4-ethynylphenyl)-4-propyl-2,6,7-trioxabicyclo(2.2.2)octane) | Studies (oleylamide) | Trials (oleylamide) | Recent Studies (post-2010) (oleylamide) |
|---|---|---|---|---|---|
| 40 | 0 | 5 | 197 | 0 | 63 |
| Protein | Taxonomy | 1-(4-ethynylphenyl)-4-propyl-2,6,7-trioxabicyclo(2.2.2)octane (IC50) | oleylamide (IC50) |
|---|---|---|---|
| Transient receptor potential cation channel subfamily V member 2 | Rattus norvegicus (Norway rat) | 2.1 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Coyne, L; Lees, G; Neufield, KD; Nicholson, RA; Zheng, J | 1 |
1 other study(ies) available for 1-(4-ethynylphenyl)-4-propyl-2,6,7-trioxabicyclo(2.2.2)octane and oleylamide
| Article | Year |
|---|---|
The sleep hormone oleamide modulates inhibitory ionotropic receptors in mammalian CNS in vitro.
Topics: Animals; Biological Transport, Active; Brain; Bridged Bicyclo Compounds, Heterocyclic; Chloride Channels; Female; GABA-A Receptor Agonists; GABA-A Receptor Antagonists; gamma-Aminobutyric Acid; Glycine; Humans; Hypnotics and Sedatives; Male; Mice; Muscimol; Oleic Acids; Oocytes; Radioligand Assay; Receptors, GABA-A; Receptors, Glycine; Sleep; Synaptic Membranes; Tritium; Xenopus laevis | 2002 |