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1,3-dipropyl-8-(2-amino-4-chlorophenyl)xanthine and 8-phenyltheophylline

1,3-dipropyl-8-(2-amino-4-chlorophenyl)xanthine has been researched along with 8-phenyltheophylline in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jacobson, KA; van Galen, PJ; Williams, M1
Butts-Lamb, P; Daly, JW; Padgett, W; Shamim, MT; Waters, J1
Badger, EW; Bristol, JA; Bruns, RF; Haleen, SJ; Hamilton, HW; Ortwine, DF; Steffen, RP; Worth, DF1
Burnstock, G; Hoyle, CH1
Braunwalder, A; Ferkany, JW; Jarvis, MF; Sills, MA; Williams, M1

Reviews

1 review(s) available for 1,3-dipropyl-8-(2-amino-4-chlorophenyl)xanthine and 8-phenyltheophylline

ArticleYear
Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential.
    Journal of medicinal chemistry, 1992, Feb-07, Volume: 35, Issue:3

    Topics: Adenosine; Animals; Humans; Models, Chemical; Receptors, Purinergic; Second Messenger Systems; Structure-Activity Relationship

1992

Other Studies

4 other study(ies) available for 1,3-dipropyl-8-(2-amino-4-chlorophenyl)xanthine and 8-phenyltheophylline

ArticleYear
1,3-Dialkyl-8-(p-sulfophenyl)xanthines: potent water-soluble antagonists for A1- and A2-adenosine receptors.
    Journal of medicinal chemistry, 1985, Volume: 28, Issue:4

    Topics: Adenosine; Animals; Cerebral Cortex; In Vitro Techniques; Rats; Receptors, Cell Surface; Receptors, Purinergic; Solubility; Structure-Activity Relationship

1985
Synthesis of xanthines as adenosine antagonists, a practical quantitative structure-activity relationship application.
    Journal of medicinal chemistry, 1985, Volume: 28, Issue:8

    Topics: Adenosine; Animals; Brain; Cattle; Heart; In Vitro Techniques; Rats; Receptors, Cell Surface; Receptors, Purinergic; Structure-Activity Relationship; Xanthines

1985
PACPX--a substituted xanthine--antagonizes both the A1 and A2 subclasses of the P1-purinoceptor: antagonism of the A2 subclass is competitive but antagonism of the A1 subclass is not.
    British journal of pharmacology, 1985, Volume: 85, Issue:1

    Topics: Adenosine; Animals; Binding, Competitive; Colon; Dipyridamole; Female; Guinea Pigs; In Vitro Techniques; Male; Muscle, Smooth; Myocardial Contraction; Norepinephrine; Receptors, Neurotransmitter; Receptors, Purinergic; Theophylline; Xanthines

1985
Biochemical characterization of the antagonist actions of the xanthines, PACPX (1,3-dipropyl-8(2-amino-4-chloro)phenylxanthine) and 8-PT (8-phenyltheophylline) at adenosine A1 and A2 receptors in rat brain tissue.
    Biochemical pharmacology, 1987, Nov-15, Volume: 36, Issue:22

    Topics: Adenosine; Adenosine-5'-(N-ethylcarboxamide); Animals; Brain; In Vitro Techniques; Kinetics; Rats; Receptors, Purinergic; Theophylline; Xanthines

1987