8-phenyltheophylline has been researched along with 1,3-dipropyl-8-(4-sulfophenyl)xanthine in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 2 (28.57) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Daly, JW; Padgett, WL; Shamim, MT; Ukena, D | 1 |
| Butts-Lamb, P; Daly, JW; Padgett, W; Shamim, MT; Waters, J | 1 |
| Badger, EW; Bristol, JA; Bruns, RF; Haleen, SJ; Hamilton, HW; Ortwine, DF; Steffen, RP; Worth, DF | 1 |
| Daly, JW; Gallo-Rodriguez, C; Jacobson, KA; Kiriasis, L; Manning, M; Müller, C; Neumeyer, JL; Pfleiderer, W; Shi, D | 1 |
| Müller, CE; Yan, L | 1 |
| Bellows, DS; Clarke, ID; Diamandis, P; Dirks, PB; Graham, J; Jamieson, LG; Ling, EK; Sacher, AG; Tyers, M; Ward, RJ; Wildenhain, J | 1 |
| d'Almeida, MS; Lautt, WW; Zhang, Y | 1 |
7 other study(ies) available for 8-phenyltheophylline and 1,3-dipropyl-8-(4-sulfophenyl)xanthine
| Article | Year |
|---|---|
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.
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 |
1,3-Dialkyl-8-(p-sulfophenyl)xanthines: potent water-soluble antagonists for A1- and A2-adenosine receptors.
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.
Topics: Adenosine; Animals; Brain; Cattle; Heart; In Vitro Techniques; Rats; Receptors, Cell Surface; Receptors, Purinergic; Structure-Activity Relationship; Xanthines | 1985 |
Effect of trifluoromethyl and other substituents on activity of xanthines at adenosine receptors.
Topics: Acylation; Alkylation; Animals; Brain; Caffeine; Cell Membrane; Cyclization; Molecular Structure; Purinergic P1 Receptor Antagonists; Rats; Receptors, Purinergic P1; Structure-Activity Relationship; Trifluoroacetic Acid; Xanthines | 1993 |
Preparation, properties, reactions, and adenosine receptor affinities of sulfophenylxanthine nitrophenyl esters: toward the development of sulfonic acid prodrugs with peroral bioavailability.
Topics: Adenosine A1 Receptor Antagonists; Adenosine A2 Receptor Antagonists; Administration, Oral; Animals; Biological Availability; Brain; Cattle; Cell Line; Cricetinae; Drug Stability; Esters; Humans; Hydrolysis; In Vitro Techniques; Liver; Nitrobenzenes; Prodrugs; Purinergic P1 Receptor Antagonists; Radioligand Assay; Rats; Receptors, Purinergic P1; Structure-Activity Relationship; Sulfonic Acids; Xanthines | 2004 |
Chemical genetics reveals a complex functional ground state of neural stem cells.
Topics: Animals; Cell Survival; Cells, Cultured; Mice; Molecular Structure; Neoplasms; Neurons; Pharmaceutical Preparations; Sensitivity and Specificity; Stem Cells | 2007 |
Determination of the effectiveness of DPSPS as an adenosine receptor antagonist in vivo.
Topics: Adenosine; Animals; Cats; Female; Hepatic Artery; Isoproterenol; Male; Mesenteric Arteries; Muscle, Smooth, Vascular; Neural Conduction; Purinergic Antagonists; Theophylline; Xanthines | 1990 |