flufenamic acid has been researched along with phenylephrine in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
| Inoue, R; Ito, Y; Waniishi, Y; Yamada, K | 1 |
| Hara, Y; Inoue, R; Ito, Y; Mori, Y; Naitoh, S; Okada, T; Onoue, H; Shimizu, S | 1 |
3 other study(ies) available for flufenamic acid and phenylephrine
| Article | Year |
|---|---|
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Fenamates potentiate the alpha 1-adrenoceptor-activated nonselective cation channels in rabbit portal vein smooth muscle.
Topics: Adrenergic alpha-Agonists; Animals; Cations; Drug Synergism; Flufenamic Acid; Ion Channels; Male; Mefenamic Acid; Muscle, Smooth, Vascular; ortho-Aminobenzoates; Patch-Clamp Techniques; Phenylephrine; Portal Vein; Rabbits; Receptors, Adrenergic, alpha-1 | 1996 |
The transient receptor potential protein homologue TRP6 is the essential component of vascular alpha(1)-adrenoceptor-activated Ca(2+)-permeable cation channel.
Topics: Adrenergic alpha-Agonists; Animals; Barium; Cadmium; Calcium; Calcium Channels; Cations; Cell Line; Cells, Cultured; CHO Cells; Cricetinae; DNA, Antisense; Dose-Response Relationship, Drug; Drug Synergism; Flufenamic Acid; Gene Expression; Humans; Ion Channels; Membrane Potentials; Mice; Muscle, Smooth, Vascular; Patch-Clamp Techniques; Phenylephrine; Portal Vein; Rabbits; RNA, Messenger; TRPC Cation Channels | 2001 |