2,5-dimethoxy-4-bromoamphetamine has been researched along with mescaline in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Glennon, RA; Liebowitz, SM; Mack, EC | 1 |
Anderson, GM; Glennon, RA; Liebowitz, SM | 1 |
Clare, BW | 1 |
Chambers, JJ; Jensen, NH; Kurrasch-Orbaugh, DM; Marona-Lewicka, D; Nichols, DE; Parrish, JC | 1 |
Kurrasch, DM; Nichols, DE; Parker, MA | 1 |
Berg, KA; Cassels, BK; Clarke, WP; Gutiérrez-Hernandez, MA; Moya, PR; Reyes-Parada, M; Sáez-Briones, P | 1 |
6 other study(ies) available for 2,5-dimethoxy-4-bromoamphetamine and mescaline
Article | Year |
---|---|
Serotonin receptor binding affinities of several hallucinogenic phenylalkylamine and N,N-dimethyltryptamine analogues.
Topics: Amines; Animals; Female; Hallucinogens; In Vitro Techniques; Male; Muscle Contraction; Muscle, Smooth; N,N-Dimethyltryptamine; Rats; Receptors, Serotonin; Stomach; Tryptamines | 1978 |
Serotonin receptor affinities of psychoactive phenalkylamine analogues.
Topics: Amines; Animals; Female; Hallucinogens; In Vitro Techniques; Male; Muscle Contraction; Muscle, Smooth; Rats; Receptors, Serotonin; Stomach; Structure-Activity Relationship | 1980 |
The frontier orbital phase angles: novel QSAR descriptors for benzene derivatives, applied to phenylalkylamine hallucinogens.
Topics: Hallucinogens; Humans; Models, Molecular; Molecular Conformation; Phenethylamines; Quantum Theory | 1998 |
Synthesis and pharmacological characterization of a series of geometrically constrained 5-HT(2A/2C) receptor ligands.
Topics: Animals; Binding, Competitive; Cells, Cultured; Discrimination Learning; Furans; Heterocyclic Compounds, 3-Ring; Inositol Phosphates; Ligands; Lysergic Acid Diethylamide; Male; Molecular Conformation; Radioligand Assay; Rats; Rats, Sprague-Dawley; Receptor, Serotonin, 5-HT2A; Receptor, Serotonin, 5-HT2C; Receptors, Serotonin; Receptors, Serotonin, 5-HT1; Serotonin Receptor Agonists; Stereoisomerism; Structure-Activity Relationship | 2003 |
The role of lipophilicity in determining binding affinity and functional activity for 5-HT2A receptor ligands.
Topics: Anthracenes; Catalysis; Hydrophobic and Hydrophilic Interactions; Ligands; Lipids; Molecular Structure; Phenethylamines; Protein Binding; Receptor, Serotonin, 5-HT2A; Serotonin Antagonists; Serotonin Receptor Agonists | 2008 |
Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A and 5-HT2C receptors.
Topics: Amphetamines; Animals; Arachidonic Acid; Behavior, Animal; CHO Cells; Cricetinae; Cricetulus; DOM 2,5-Dimethoxy-4-Methylamphetamine; Hallucinogens; Humans; Inositol Phosphates; Male; Mescaline; Motor Activity; Phenethylamines; Rats; Rats, Sprague-Dawley; Receptor, Serotonin, 5-HT2A; Receptor, Serotonin, 5-HT2C; Serotonin 5-HT2 Receptor Agonists; Signal Transduction; Transfection | 2007 |