1,3-dipropyl-8-cyclopentylxanthine and 1,3-dipropyl-8-phenylxanthine

1,3-dipropyl-8-cyclopentylxanthine has been researched along with 1,3-dipropyl-8-phenylxanthine in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19903 (50.00)18.7374
1990's2 (33.33)18.2507
2000's1 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ijzerman, AP; Soudijn, W; van der Wenden, EM1
Abreu, ME; Blake, PR; Costello, DG; Erickson, RH; Feeney, SW; Hicks, RP; Hiner, RN; Rzeszotarski, WJ1
Daly, JW; Padgett, WL; Shamim, MT; Ukena, D1
Barone, S; Bradbury, BJ; Campagne, JM; Daly, JW; Jacobson, KA; Kammula, U; Kiriasis, L; Neumeyer, JL; Pfleiderer, W; Secunda, S1
Daly, JW; Hong, O; Padgett, WL; Shamim, MT; Ukena, D1
Jacobson, KA; Kim, HS; Kim, SA; Linden, J; Marshall, MA; Melman, N; Müller, CE1

Other Studies

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

ArticleYear
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
1,3,8-trisubstituted xanthines. Effects of substitution pattern upon adenosine receptor A1/A2 affinity.
    Journal of medicinal chemistry, 1991, Volume: 34, Issue:4

    Topics: Animals; Cell Membrane; Corpus Striatum; Indicators and Reagents; Kinetics; Molecular Structure; Rats; Receptors, Purinergic; Structure-Activity Relationship; Xanthines

1991
Effects of 8-phenyl and 8-cycloalkyl substituents on the activity of mono-, di-, and trisubstituted alkylxanthines with substitution at the 1-, 3-, and 7-positions.
    Journal of medicinal chemistry, 1989, Volume: 32, Issue:6

    Topics: Adenylyl Cyclases; Adipose Tissue; Adrenal Gland Neoplasms; Animals; Blood Platelets; Brain; Caffeine; Chemical Phenomena; Chemistry; Humans; Molecular Structure; Phenylisopropyladenosine; Pheochromocytoma; Rats; Receptors, Purinergic; Structure-Activity Relationship; Theophylline; Tumor Cells, Cultured; Xanthines

1989
Sulfur-containing 1,3-dialkylxanthine derivatives as selective antagonists at A1-adenosine receptors.
    Journal of medicinal chemistry, 1989, Volume: 32, Issue:8

    Topics: Animals; Binding, Competitive; Chemical Phenomena; Chemistry; In Vitro Techniques; Radioligand Assay; Rats; Receptors, Purinergic; Structure-Activity Relationship; Sulfur; Xanthines

1989
8-Aryl-and 8-cycloalkyl-1,3-dipropylxanthines: further potent and selective antagonists for A1-adenosine receptors.
    Journal of medicinal chemistry, 1988, Volume: 31, Issue:3

    Topics: Adenylyl Cyclase Inhibitors; Animals; Guinea Pigs; Humans; In Vitro Techniques; Kinetics; Phenylisopropyladenosine; Rats; Receptors, Purinergic; Solubility; Structure-Activity Relationship; Xanthines

1988
Structure-activity relationships at human and rat A2B adenosine receptors of xanthine derivatives substituted at the 1-, 3-, 7-, and 8-positions.
    Journal of medicinal chemistry, 2002, May-23, Volume: 45, Issue:11

    Topics: Animals; Binding, Competitive; Cell Line; Cloning, Molecular; Humans; Ligands; Purinergic P1 Receptor Antagonists; Radioligand Assay; Rats; Rats, Sprague-Dawley; Receptor, Adenosine A2B; Receptors, Purinergic P1; Recombinant Proteins; Structure-Activity Relationship; Xanthines

2002