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4-ethoxyamphetamine and 4-iodo-2,5-dimethoxyphenylisopropylamine

4-ethoxyamphetamine has been researched along with 4-iodo-2,5-dimethoxyphenylisopropylamine in 2 studies

*4-iodo-2,5-dimethoxyphenylisopropylamine: RN given refers to unlabeled parent cpd without isomeric designation; a serotonin agonist [MeSH]

Compound Research Comparison

Studies (4-ethoxyamphetamine)	Trials (4-ethoxyamphetamine)	Recent Studies (post-2010) (4-ethoxyamphetamine)	Studies (4-iodo-2,5-dimethoxyphenylisopropylamine)	Trials (4-iodo-2,5-dimethoxyphenylisopropylamine)	Recent Studies (post-2010) (4-iodo-2,5-dimethoxyphenylisopropylamine)
7	0	0	843	1	127

Protein Interaction Comparison

Protein	Taxonomy	4-ethoxyamphetamine (IC50)	4-iodo-2,5-dimethoxyphenylisopropylamine (IC50)
5-hydroxytryptamine receptor 2B	Homo sapiens (human)		0.0032

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bartyzel, P; Glennon, RA; Leonhardt, S; Raghupathi, R; Teitler, M	1
Cassels, BK; Castillo, M; Fierro, A; Gallardo-Godoy, A; McLean, TH; Nichols, DE; Reyes-Parada, M	1

Other Studies

2 other study(ies) available for 4-ethoxyamphetamine and 4-iodo-2,5-dimethoxyphenylisopropylamine

Article	Year
Binding of phenylalkylamine derivatives at 5-HT1C and 5-HT2 serotonin receptors: evidence for a lack of selectivity. Journal of medicinal chemistry, 1992, Feb-21, Volume: 35, Issue:4 Topics: Animals; Binding Sites; Binding, Competitive; Ergolines; Ketanserin; Male; Molecular Structure; Propylamines; Rats; Rats, Inbred Strains; Receptors, Serotonin; Structure-Activity Relationship; Tritium	1992
Sulfur-substituted alpha-alkyl phenethylamines as selective and reversible MAO-A inhibitors: biological activities, CoMFA analysis, and active site modeling. Journal of medicinal chemistry, 2005, Apr-07, Volume: 48, Issue:7 Topics: Animals; Binding Sites; Brain; Clorgyline; Crystallography, X-Ray; In Vitro Techniques; Male; Methylation; Mitochondria; Models, Molecular; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Quantitative Structure-Activity Relationship; Rats; Rats, Sprague-Dawley	2005

Article

Year

Binding of phenylalkylamine derivatives at 5-HT1C and 5-HT2 serotonin receptors: evidence for a lack of selectivity.

Journal of medicinal chemistry, 1992, Feb-21, Volume: 35, Issue:4

Topics: Animals; Binding Sites; Binding, Competitive; Ergolines; Ketanserin; Male; Molecular Structure; Propylamines; Rats; Rats, Inbred Strains; Receptors, Serotonin; Structure-Activity Relationship; Tritium

1992

Sulfur-substituted alpha-alkyl phenethylamines as selective and reversible MAO-A inhibitors: biological activities, CoMFA analysis, and active site modeling.

Journal of medicinal chemistry, 2005, Apr-07, Volume: 48, Issue:7

Topics: Animals; Binding Sites; Brain; Clorgyline; Crystallography, X-Ray; In Vitro Techniques; Male; Methylation; Mitochondria; Models, Molecular; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Quantitative Structure-Activity Relationship; Rats; Rats, Sprague-Dawley

2005