haloperidol has been researched along with bd 1063 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 | 1 (33.33) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Bowen, WD; de Costa, BR; Dominguez, C; Gu, ZQ; He, XS; Linders, JT; Williams, W | 1 |
Almansa, C; Berrocal, J; Burgueño, J; Buschmann, H; Christmann, U; Contijoch, M; Cuberes, R; Díaz, JL; Fernández, A; Holenz, J; Laggner, C; Merlos, M; Port, A; Serafini, MT; Vela, JM; Zamanillo, D | 1 |
Amata, E; Artacho-Cordón, A; Barbaraci, C; Cobos, EJ; Dichiara, M; Gómez-Guzmán, M; González-Cano, R; Marrazzo, A; Pasquinucci, L; Rodríguez-Gómez, I; Santos-Caballero, M; Turnaturi, R | 1 |
3 other study(ies) available for haloperidol and bd 1063
Article | Year |
---|---|
Synthesis and evaluation of conformationally restricted N-[2-(3,4-dichlorophenyl)ethyl]-N-methyl-2-(1-pyrrolidinyl)ethylamines at sigma receptors. 2. Piperazines, bicyclic amines, bridged bicyclic amines, and miscellaneous compounds.
Topics: Animals; Brain; Ethylamines; Guinea Pigs; Receptors, sigma; Structure-Activity Relationship | 1993 |
Synthesis and biological evaluation of the 1-arylpyrazole class of σ(1) receptor antagonists: identification of 4-{2-[5-methyl-1-(naphthalen-2-yl)-1H-pyrazol-3-yloxy]ethyl}morpholine (S1RA, E-52862).
Topics: Animals; Brain; Female; Guinea Pigs; HEK293 Cells; Humans; Hyperalgesia; In Vitro Techniques; Male; Mice; Microsomes, Liver; Morpholines; Motor Activity; Neuralgia; Patch-Clamp Techniques; Pyrazoles; Radioligand Assay; Receptors, sigma; Sciatic Neuropathy; Sigma-1 Receptor; Structure-Activity Relationship | 2012 |
Dual Sigma-1 receptor antagonists and hydrogen sulfide-releasing compounds for pain treatment: Design, synthesis, and pharmacological evaluation.
Topics: Animals; Guinea Pigs; Hydrogen; Hydrogen Sulfide; Ligands; Male; Morpholines; Pain; Piperazines; Rats, Sprague-Dawley; Receptors, sigma; Sigma-1 Receptor | 2022 |