atropine has been researched along with alpha-methylhistamine in 3 studies
| Studies (atropine) | Trials (atropine) | Recent Studies (post-2010) (atropine) | Studies (alpha-methylhistamine) | Trials (alpha-methylhistamine) | Recent Studies (post-2010) (alpha-methylhistamine) |
|---|---|---|---|---|---|
| 26,711 | 1,259 | 1,697 | 240 | 3 | 13 |
| 26,711 | 1,259 | 1,697 | 46 | 0 | 12 |
| Protein | Taxonomy | atropine (IC50) | alpha-methylhistamine (IC50) |
|---|---|---|---|
| Histamine H3 receptor | Rattus norvegicus (Norway rat) | 0.0015 | |
| Histamine H3 receptor | Homo sapiens (human) | 0.0023 |
| 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 |
|---|---|
| Bast, A; Scheerens, H; Timmerman, H; Vollinga, RC; Zuiderveld, OP | 1 |
| Murakami, Y; Nakamura, K; Okada, S; Wang, M; Yokotani, K | 1 |
| Hayashi, S; Kato, A; Mizuno, K; Morita, A; Nakata, E; Ohashi, K; Yamamura, K | 1 |
3 other study(ies) available for atropine and alpha-methylhistamine
| Article | Year |
|---|---|
A simple and rapid in vitro test system for the screening of histamine H3 ligands.
Topics: Acetylcholine; Animals; Atropine; Drug Evaluation, Preclinical; Electric Stimulation; Guinea Pigs; Histamine Agonists; In Vitro Techniques; Isotonic Contraction; Jejunum; Ligands; Male; Methylhistamines; Muscle Contraction; Piperidines; Receptors, Histamine; Receptors, Histamine H3 | 1992 |
Histamine H(3) receptor-mediated inhibition of endogenous acetylcholine release from the isolated, vascularly perfused rat stomach.
Topics: Acetylcholine; Animals; Atropine; Gastric Mucosa; GTP-Binding Proteins; Histamine; Imidazoles; Male; Methylhistamines; Perfusion; Pertussis Toxin; Piperidines; Rats; Rats, Wistar; Receptors, Histamine H3; Thiourea; Vagus Nerve; Virulence Factors, Bordetella | 2000 |
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 |