glyburide has been researched along with alpha-methylhistamine 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 | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ohkubo, T; Shibata, M | 1 |
| Hayashi, S; Kato, A; Mizuno, K; Morita, A; Nakata, E; Ohashi, K; Yamamura, K | 1 |
| Carmody, LC; Dandapani, S; Donckele, E; Feng, Y; Fernandez, C; Germain, AR; Gupta, PB; Lander, ES; Morgan, B; Munoz, B; Nag, PP; Palmer, M; Perez, JR; Schreiber, SL; Verplank, L | 1 |
3 other study(ies) available for glyburide and alpha-methylhistamine
| Article | Year |
|---|---|
ATP-sensitive K+ channels mediate regulation of substance P release via the prejunctional histamine H3 receptor.
Topics: Adenosine Triphosphate; Analysis of Variance; Animals; Benzopyrans; Cromakalim; Glyburide; Hindlimb; Histamine Agonists; Injections, Intravenous; Male; Methylhistamines; Neuromuscular Junction; Potassium Channel Blockers; Potassium Channels; Pyrroles; Radioimmunoassay; Rats; Rats, Wistar; Receptors, Histamine H3; Skin; Stereoisomerism; Substance P; Tetraethylammonium; Tetraethylammonium Compounds; Vasodilator Agents | 1995 |
Discovery of {1-[4-(2-{hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}-1H-benzimidazol-1-yl)piperidin-1-yl]cyclooctyl}methanol, systemically potent novel non-peptide agonist of nociceptin/orphanin FQ receptor as analgesic for the treatment of neuropathic pain: de
Topics: Analgesics; Animals; Benzimidazoles; Drug Design; Drug Evaluation, Preclinical; Humans; Microsomes, Liver; Neuralgia; Nociceptin Receptor; Pyrroles; Rats; Receptors, Opioid; Structure-Activity Relationship | 2010 |
Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells.
Topics: Amides; Breast Neoplasms; Cell Line, Tumor; Drug Screening Assays, Antitumor; Female; Humans; Neoplastic Stem Cells; Small Molecule Libraries; Structure-Activity Relationship | 2013 |