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

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

*8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine: adenosine receptor antagonist [MeSH]

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 (8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine)	Trials (8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine)	Recent Studies (post-2010) (8-(4-((2-aminoethyl)aminocarbonylmethyloxy)phenyl)-1,3-dipropylxanthine)
6	0	0	108	0	14

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
Olah, M; Stiles, GL	1
Bourgoin, S; Cesselin, F; Hamon, M; Mauborgne, A; Poliénor, H	1

Other Studies

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

Article	Year
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

Article

Year

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