Page last updated: 2024-09-05

mdl 72832 and 8-hydroxy-2-(di-n-propylamino)tetralin

mdl 72832 has been researched along with 8-hydroxy-2-(di-n-propylamino)tetralin in 1 studies

*8-Hydroxy-2-(di-n-propylamino)tetralin: A serotonin 1A-receptor agonist that is used experimentally to test the effects of serotonin. [MeSH]

*8-Hydroxy-2-(di-n-propylamino)tetralin: A serotonin 1A-receptor agonist that is used experimentally to test the effects of serotonin. [MeSH]

Compound Research Comparison

Studies
(mdl 72832)
Trials
(mdl 72832)
Recent Studies (post-2010)
(mdl 72832)
Studies
(8-hydroxy-2-(di-n-propylamino)tetralin)
Trials
(8-hydroxy-2-(di-n-propylamino)tetralin)
Recent Studies (post-2010) (8-hydroxy-2-(di-n-propylamino)tetralin)
7023,5307389

Protein Interaction Comparison

ProteinTaxonomymdl 72832 (IC50)8-hydroxy-2-(di-n-propylamino)tetralin (IC50)
5-hydroxytryptamine receptor 1AHomo sapiens (human)0.0012
5-hydroxytryptamine receptor 1ARattus norvegicus (Norway rat)0.0032
Alpha-2B adrenergic receptorRattus norvegicus (Norway rat)0.81
D(2) dopamine receptorBos taurus (cattle)0.8
Alpha-2C adrenergic receptorRattus norvegicus (Norway rat)0.81
Alpha-2A adrenergic receptorRattus norvegicus (Norway rat)0.81
D(2) dopamine receptorRattus norvegicus (Norway rat)2.8959
Lysosomal alpha-glucosidaseBos taurus (cattle)0.0021

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fozard, JR; Gittos, MW; Hibert, MF; Middlemiss, DN; Mir, AK1

Other Studies

1 other study(ies) available for mdl 72832 and 8-hydroxy-2-(di-n-propylamino)tetralin

ArticleYear
Graphics computer-aided receptor mapping as a predictive tool for drug design: development of potent, selective, and stereospecific ligands for the 5-HT1A receptor.
    Journal of medicinal chemistry, 1988, Volume: 31, Issue:6

    Topics: Animals; Computer Graphics; In Vitro Techniques; Ligands; Molecular Conformation; Rats; Receptors, Serotonin; Serotonin Antagonists; Stereoisomerism; Structure-Activity Relationship

1988