tetraethylammonium has been researched along with ginsenoside rg3 in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kang, SY; Kim, ND; Park, JH; Schini-Kerth, VB | 1 |
| Kang, SY; Kim, MJ; Kim, ND; Park, JH; Schini-Kerth, VB | 1 |
| Choe, H; Choi, SH; Choi, WS; Kim, DH; Kim, YI; Lee, BH; Lee, JH; Lim, Y; Lim, YW; Nah, SY; Pyo, MK; Rhim, H; Shin, TJ; Won, KH; Yoon, IS | 1 |
| Choi, SH; Ha, TS; Hwang, SH; Lee, BC; Lee, BH; Lee, SM; Nah, SY; Park, CS; Shin, TJ | 1 |
4 other study(ies) available for tetraethylammonium and ginsenoside rg3
| Article | Year |
|---|---|
Ginsenoside Rg3 mediates endothelium-dependent relaxation in response to ginsenosides in rat aorta: role of K+ channels.
Topics: Adrenergic beta-Antagonists; Animals; Antineoplastic Agents, Phytogenic; Aorta, Thoracic; Atropine; Calcium Channel Blockers; Chromatography, High Pressure Liquid; Diphenhydramine; Dose-Response Relationship, Drug; Endothelium, Vascular; Ginsenosides; Glyburide; Histamine H1 Antagonists; In Vitro Techniques; Male; Muscarinic Antagonists; Muscle Relaxation; Nitroprusside; Potassium Channel Blockers; Potassium Channels; Propranolol; Rats; Rats, Sprague-Dawley; Sapogenins; Saponins; Tetraethylammonium; Triterpenes; Vasodilator Agents; Vasomotor System | 1999 |
The ginsenoside Rg3 evokes endothelium-independent relaxation in rat aortic rings: role of K+ channels.
Topics: Animals; Antineoplastic Agents, Phytogenic; Aorta, Thoracic; Calcium; Calcium Channel Blockers; Cromakalim; Dose-Response Relationship, Drug; Endothelium, Vascular; Ginsenosides; Glyburide; In Vitro Techniques; Male; Muscle Relaxation; Nifedipine; Potassium Channel Blockers; Potassium Channels; Potassium Chloride; Rats; Rats, Sprague-Dawley; Rubidium Radioisotopes; Saponins; Tetraethylammonium; Vasodilator Agents | 1999 |
Ginsenoside Rg3 inhibits human Kv1.4 channel currents by interacting with the Lys531 residue.
Topics: Amino Acid Substitution; Animals; Binding Sites; Dose-Response Relationship, Drug; Female; Ginsenosides; Humans; Hydrogen Bonding; Inhibitory Concentration 50; Kv1.4 Potassium Channel; Lysine; Models, Molecular; Molecular Structure; Oocytes; Patch-Clamp Techniques; Potassium Channel Blockers; Protein Binding; Tetraethylammonium; Xenopus laevis | 2008 |
Ginsenoside Rg3 enhances large conductance Ca2+-activated potassium channel currents: a role of Tyr360 residue.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Calcium; Ginsenosides; Intracellular Space; Ion Channel Gating; Large-Conductance Calcium-Activated Potassium Channels; Molecular Sequence Data; Mutant Proteins; Mutation; Oocytes; Patch-Clamp Techniques; Rats; Structure-Activity Relationship; Tetraethylammonium; Tyrosine; Xenopus | 2011 |