1,3-dipropyl-8-phenylxanthine and n(6)-phenyladenosine

1,3-dipropyl-8-phenylxanthine has been researched along with n(6)-phenyladenosine in 2 studies

Compound Research Comparison

Studies (1,3-dipropyl-8-phenylxanthine)	Trials (1,3-dipropyl-8-phenylxanthine)	Recent Studies (post-2010) (1,3-dipropyl-8-phenylxanthine)	Studies (n(6)-phenyladenosine)	Trials (n(6)-phenyladenosine)	Recent Studies (post-2010) (n(6)-phenyladenosine)
35	0	8	28	0	6

Protein Interaction Comparison

Protein	Taxonomy	n(6)-phenyladenosine (IC50)
neuropeptide Y receptor type 1	Homo sapiens (human)	7.826
neuropeptide Y receptor type 2	Homo sapiens (human)	4.729
Adenosine receptor A1	Rattus norvegicus (Norway rat)	0.0049
Adenosine receptor A2b	Rattus norvegicus (Norway rat)	0.66
Adenosine receptor A2a	Rattus norvegicus (Norway rat)	0.66
Adenosine receptor A1	Gallus gallus (chicken)	0.0046

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ijzerman, AP; Soudijn, W; van der Wenden, EM	1
Barone, S; Daly, JW; Jacobson, KA; Kirk, KL; Schulick, R; Zimmet, J	1

Other Studies

2 other study(ies) available for 1,3-dipropyl-8-phenylxanthine and n(6)-phenyladenosine

Article	Year
A steric and electrostatic comparison of three models for the agonist/antagonist binding site on the adenosine A1 receptor. Journal of medicinal chemistry, 1992, Feb-21, Volume: 35, Issue:4 Topics: Adenosine; Binding Sites; Chemical Phenomena; Chemistry, Physical; Electrochemistry; Models, Molecular; Molecular Conformation; Molecular Structure; Purinergic Antagonists; Receptors, Purinergic; Regression Analysis; Structure-Activity Relationship; Xanthine; Xanthines	1992
Adenosine analogs with covalently attached lipids have enhanced potency at A1-adenosine receptors. FEBS letters, 1987, Dec-10, Volume: 225, Issue:1-2 Topics: Adenosine; Aniline Compounds; Animals; Cell Membrane; Cerebral Cortex; Chemical Phenomena; Chemistry; Diglycerides; Fatty Acids; Lipid Metabolism; Phenylisopropyladenosine; Phosphatidylethanolamines; Prodrugs; Rats; Receptors, Purinergic; Xanthines	1987

Article

Year

A steric and electrostatic comparison of three models for the agonist/antagonist binding site on the adenosine A1 receptor.

Journal of medicinal chemistry, 1992, Feb-21, Volume: 35, Issue:4

Topics: Adenosine; Binding Sites; Chemical Phenomena; Chemistry, Physical; Electrochemistry; Models, Molecular; Molecular Conformation; Molecular Structure; Purinergic Antagonists; Receptors, Purinergic; Regression Analysis; Structure-Activity Relationship; Xanthine; Xanthines

1992

Adenosine analogs with covalently attached lipids have enhanced potency at A1-adenosine receptors.

FEBS letters, 1987, Dec-10, Volume: 225, Issue:1-2

Topics: Adenosine; Aniline Compounds; Animals; Cell Membrane; Cerebral Cortex; Chemical Phenomena; Chemistry; Diglycerides; Fatty Acids; Lipid Metabolism; Phenylisopropyladenosine; Phosphatidylethanolamines; Prodrugs; Rats; Receptors, Purinergic; Xanthines

1987