caffeic acid phenethyl ester has been researched along with Pain 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 | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Antonini, G; Cechinel Filho, V; de Campos Buzzi, F; Fracasso, M; Franzoi, CL; Niero, R; Yunes, RA | 1 |
| Bennis, K; Busserolles, J; C Chatelain, F; Chapuy, E; Deokar, H; Ducki, S; Eschalier, A; Lesage, F; Pereira, V; Rodrigues, N; Vivier, D | 1 |
| Bennis, K; Ducki, S; Lesage, F; Vivier, D | 1 |
1 review(s) available for caffeic acid phenethyl ester and Pain
| Article | Year |
|---|---|
Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K(+) Channel 1). A Novel Therapeutic Target?
Topics: Arrhythmias, Cardiac; Depression; Epilepsy; Humans; Inflammation; Models, Molecular; Molecular Structure; Neuroprotective Agents; Pain; Potassium Channels, Tandem Pore Domain; Structure-Activity Relationship | 2016 |
2 other study(ies) available for caffeic acid phenethyl ester and Pain
| Article | Year |
|---|---|
Antinociceptive properties of caffeic acid derivatives in mice.
Topics: Analgesics; Animals; Caffeic Acids; Mice; Molecular Structure; Pain; Structure-Activity Relationship | 2009 |
Synthesis and structure-activity relationship study of substituted caffeate esters as antinociceptive agents modulating the TREK-1 channel.
Topics: Analgesics; Animals; Caffeic Acids; Cinnamates; Esters; Male; Mice; Models, Molecular; Pain; Potassium Channels, Tandem Pore Domain; Quantitative Structure-Activity Relationship; Xenopus | 2014 |