haloperidol has been researched along with nemonapride in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 2 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Hasegawa, O; Hirata, Y; Iwanami, S; Takashima, M; Usuda, S | 1 |
Demattos, S; MacKenzie, RG; O'Malley, KL; Pugsley, TA; Shih, YH; Tang, L; Todd, RD; VanLeeuwen, D | 1 |
Hattori, H; Hidaka, K; Maeno, K; Mase, T; Matsumoto, M; Nakato, K; Ohmori, J; Sakamoto, S; Tada, S; Tsukamoto, S; Usuda, S | 1 |
Alberts, I; Harding, WW; Karki, A; Namballa, HK | 1 |
4 other study(ies) available for haloperidol and nemonapride
Article | Year |
---|---|
Synthesis and neuroleptic activity of benzamides. Cis-N-(1-benzyl-2-methylpyrrolidin-3-yl)-5-chloro-2-methoxy-4-(methylamino)benzamide and related compounds.
Topics: Animals; Antipsychotic Agents; Avoidance Learning; Benzamides; Catalepsy; Humans; Rats; Stereotyped Behavior; Structure-Activity Relationship | 1981 |
Characterization of the human dopamine D3 receptor expressed in transfected cell lines.
Topics: Animals; Arachidonic Acid; Binding, Competitive; Cell Line; CHO Cells; Cloning, Molecular; Cricetinae; Cricetulus; Cyclic AMP; Dopamine Agents; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Humans; Inositol Phosphates; Mice; Radioligand Assay; Receptors, Dopamine; Receptors, Dopamine D2; Receptors, Dopamine D3; Tetrahydronaphthalenes; Transfection | 1994 |
Dopamine D3 and D4 receptor antagonists: synthesis and structure--activity relationships of (S)-(+)-N-(1-Benzyl-3-pyrrolidinyl)-5-chloro-4- [(cyclopropylcarbonyl) amino]-2-methoxybenzamide (YM-43611) and related compounds.
Topics: Animals; Antipsychotic Agents; Benzamides; CHO Cells; Cricetinae; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Humans; Male; Mice; Mice, Inbred ICR; Motor Activity; Rats; Receptors, Dopamine D3; Receptors, Dopamine D4; Structure-Activity Relationship | 1996 |
Structural manipulation of aporphines via C10 nitrogenation leads to the identification of new 5-HT
Topics: Aporphines; Cell Line; Humans; Ligands; Molecular Docking Simulation; Molecular Structure; Receptors, Serotonin; Serotonin Antagonists; Structure-Activity Relationship | 2020 |