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8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine and n(6)-2-(4-amino-3-iodophenyl)ethyladenosine

8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine has been researched along with n(6)-2-(4-amino-3-iodophenyl)ethyladenosine in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Olah, M; Stiles, GL1
Bourgoin, S; Cesselin, F; Hamon, M; Mauborgne, A; PoliƩnor, H1

Other Studies

2 other study(ies) available for 8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine and n(6)-2-(4-amino-3-iodophenyl)ethyladenosine

ArticleYear
Agonists and antagonists recognize different but overlapping populations of A1 adenosine receptors: modulation of receptor number by MgCl2, solubilization, and guanine nucleotides.
    Journal of neurochemistry, 1990, Volume: 55, Issue:4

    Topics: Adenosine; Animals; Cattle; Cell Membrane; Cerebral Cortex; Guanosine Triphosphate; Guanylyl Imidodiphosphate; Kinetics; Magnesium Chloride; Phenylisopropyladenosine; Rats; Rats, Inbred Strains; Receptors, Purinergic; Ultracentrifugation; Xanthines

1990
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