tert-butyl peroxybenzoate has been researched along with gallamine triethiodide in 1 studies
*Gallamine Triethiodide: A synthetic nondepolarizing blocking drug. The actions of gallamine triethiodide are similar to those of TUBOCURARINE, but this agent blocks the cardiac vagus and may cause sinus tachycardia and, occasionally, hypertension and increased cardiac output. It should be used cautiously in patients at risk from increased heart rate but may be preferred for patients with bradycardia. (From AMA Drug Evaluations Annual, 1992, p198) [MeSH]
*Gallamine Triethiodide: A synthetic nondepolarizing blocking drug. The actions of gallamine triethiodide are similar to those of TUBOCURARINE, but this agent blocks the cardiac vagus and may cause sinus tachycardia and, occasionally, hypertension and increased cardiac output. It should be used cautiously in patients at risk from increased heart rate but may be preferred for patients with bradycardia. (From AMA Drug Evaluations Annual, 1992, p198) [MeSH]
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Carrington, SJ; Cho, HP; Conn, PJ; Digby, GJ; Hopkins, CR; Le, U; Lindsley, CW; Lovell, KM; Niswender, CM; Sevel, C; Sheffler, DJ; Tarr, JC; Wood, MR | 1 |
1 other study(ies) available for tert-butyl peroxybenzoate and gallamine triethiodide
| Article | Year |
|---|---|
Further exploration of M₁ allosteric agonists: subtle structural changes abolish M₁ allosteric agonism and result in pan-mAChR orthosteric antagonism.
Topics: Acetylcholine; Allosteric Regulation; Allosteric Site; Animals; Benzamides; Benzimidazoles; Calcium; CHO Cells; Cricetinae; Cricetulus; Humans; Piperidines; Rats; Receptor, Muscarinic M1; Receptors, Muscarinic; Structure-Activity Relationship; Transfection | 2013 |