Page last updated: 2024-09-03

1-propylxanthine and 8-phenyltheophylline

1-propylxanthine has been researched along with 8-phenyltheophylline in 2 studies

Compound Research Comparison

Studies (1-propylxanthine)	Trials (1-propylxanthine)	Recent Studies (post-2010) (1-propylxanthine)	Studies (8-phenyltheophylline)	Trials (8-phenyltheophylline)	Recent Studies (post-2010) (8-phenyltheophylline)
6	0	1	518	0	11

Protein Interaction Comparison

Protein	Taxonomy	8-phenyltheophylline (IC50)
Adenosine receptor A3	Homo sapiens (human)	1.25
Adenosine receptor A1	Rattus norvegicus (Norway rat)	0.2756
Adenosine receptor A1	Bos taurus (cattle)	0.003
Adenosine receptor A2a	Homo sapiens (human)	0.454
Adenosine receptor A2b	Homo sapiens (human)	0.3125
Adenosine receptor A2b	Rattus norvegicus (Norway rat)	1.1
Adenosine receptor A1	Homo sapiens (human)	1.34

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
Grahner, B; Lanzner, W; Müller, CE; Winiwarter, S	1
Jacobson, KA; Kim, HS; Kim, SA; Linden, J; Marshall, MA; Melman, N; Müller, CE	1

Other Studies

2 other study(ies) available for 1-propylxanthine and 8-phenyltheophylline

Article	Year
Synthesis and structure-activity relationships of deazaxanthines: analogs of potent A1- and A2-adenosine receptor antagonists. Journal of medicinal chemistry, 1994, May-13, Volume: 37, Issue:10 Topics: Animals; Brain; In Vitro Techniques; Purinergic P1 Receptor Antagonists; Rats; Receptors, Purinergic P1; Stereoisomerism; Structure-Activity Relationship; Xanthines	1994
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

Article

Year

Synthesis and structure-activity relationships of deazaxanthines: analogs of potent A1- and A2-adenosine receptor antagonists.

Journal of medicinal chemistry, 1994, May-13, Volume: 37, Issue:10

Topics: Animals; Brain; In Vitro Techniques; Purinergic P1 Receptor Antagonists; Rats; Receptors, Purinergic P1; Stereoisomerism; Structure-Activity Relationship; Xanthines

1994

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