Page last updated: 2024-09-03

n(6)-2-(4-amino-3-iodophenyl)ethyladenosine and substance p

n(6)-2-(4-amino-3-iodophenyl)ethyladenosine has been researched along with substance p in 1 studies

Compound Research Comparison

Studies
(n(6)-2-(4-amino-3-iodophenyl)ethyladenosine)
Trials
(n(6)-2-(4-amino-3-iodophenyl)ethyladenosine)
Recent Studies (post-2010)
(n(6)-2-(4-amino-3-iodophenyl)ethyladenosine)
Studies
(substance p)
Trials
(substance p)
Recent Studies (post-2010) (substance p)
60017,2892772,010

Protein Interaction Comparison

ProteinTaxonomyn(6)-2-(4-amino-3-iodophenyl)ethyladenosine (IC50)substance p (IC50)
Substance-P receptorRattus norvegicus (Norway rat)0.0005
Substance-K receptorRattus norvegicus (Norway rat)0.2
Substance-K receptorHomo sapiens (human)0.2455
Substance-P receptorHomo sapiens (human)0.0011
Neuromedin-K receptorHomo sapiens (human)0.125
Substance-K receptorMesocricetus auratus (golden hamster)0.148

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
Bourgoin, S; Cesselin, F; Hamon, M; Mauborgne, A; PoliƩnor, H1

Other Studies

1 other study(ies) available for n(6)-2-(4-amino-3-iodophenyl)ethyladenosine and substance p

ArticleYear
Adenosine receptor-mediated control of in vitro release of pain-related neuropeptides from the rat spinal cord.
    European journal of pharmacology, 2002, Apr-19, Volume: 441, Issue:1-2

    Topics: Adenosine; Adenosine-5'-(N-ethylcarboxamide); Animals; Calcitonin Gene-Related Peptide; Cholecystokinin; Dose-Response Relationship, Drug; In Vitro Techniques; Male; Neuropeptides; Pain; Phenethylamines; Potassium; Purinergic P1 Receptor Agonists; Purinergic P1 Receptor Antagonists; Rats; Rats, Sprague-Dawley; Receptors, Purinergic P1; Spinal Cord; Substance P; Xanthines

2002