Page last updated: 2024-09-03

l 703606 and phenylisopropyladenosine

l 703606 has been researched along with phenylisopropyladenosine in 1 studies

Compound Research Comparison

Studies
(l 703606)
Trials
(l 703606)
Recent Studies (post-2010)
(l 703606)
Studies
(phenylisopropyladenosine)
Trials
(phenylisopropyladenosine)
Recent Studies (post-2010) (phenylisopropyladenosine)
7401263010

Protein Interaction Comparison

ProteinTaxonomyl 703606 (IC50)phenylisopropyladenosine (IC50)
high affinity choline transporter 1 isoform aHomo sapiens (human)1.8613
Adenosine receptor A1Rattus norvegicus (Norway rat)0.0294
Adenosine receptor A3Rattus norvegicus (Norway rat)0.0497
Adenosine receptor A2bRattus norvegicus (Norway rat)0.2898
Adenosine receptor A1Homo sapiens (human)0.83
Adenosine receptor A2aRattus norvegicus (Norway rat)0.2898

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bergeron, C; Bolton, JL; Budzinski, JW; Dietz, BM; Foster, BC; Gafner, S; Glinski, JA; McCollom, MM; McPhail, KL; Rhyu, MR; Russell, FE; Scott, IM1

Other Studies

1 other study(ies) available for l 703606 and phenylisopropyladenosine

ArticleYear
Alkaloids from Eschscholzia californica and their capacity to inhibit binding of [3H]8-Hydroxy-2-(di-N-propylamino)tetralin to 5-HT1A receptors in Vitro.
    Journal of natural products, 2006, Volume: 69, Issue:3

    Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Alkaloids; Benzylisoquinolines; Dioxoles; Eschscholzia; Humans; Molecular Structure; Receptor, Serotonin, 5-HT1A; Serotonin Receptor Agonists

2006