1-isoamyl-3-isobutylxanthine has been researched along with theophylline in 6 studies
Studies (1-isoamyl-3-isobutylxanthine) | Trials (1-isoamyl-3-isobutylxanthine) | Recent Studies (post-2010) (1-isoamyl-3-isobutylxanthine) | Studies (theophylline) | Trials (theophylline) | Recent Studies (post-2010) (theophylline) |
---|---|---|---|---|---|
8 | 0 | 0 | 20,076 | 1,612 | 1,383 |
Protein | Taxonomy | 1-isoamyl-3-isobutylxanthine (IC50) | theophylline (IC50) |
---|---|---|---|
Adenosine receptor A1 | Bos taurus (cattle) | 2.43 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (66.67) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 1 (16.67) | 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 |
Daly, JW; Manning, M; Müller, CE; Shi, D | 1 |
Jacobson, KA; Kim, HS; Kim, SA; Linden, J; Marshall, MA; Melman, N; Müller, CE | 1 |
Daly, JW; Smellie, FW; Wells, JN | 1 |
Bittar, EE; Bittar, R; Ueno, K | 1 |
6 other study(ies) available for 1-isoamyl-3-isobutylxanthine and theophylline
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 paraxanthine analogs (1,7-disubstituted xanthines) and other xanthines unsubstituted at the 3-position: structure-activity relationships at adenosine receptors.
Topics: Animals; Brain; Radioligand Assay; Rats; Receptors, Purinergic P1; Structure-Activity Relationship; Theophylline; Xanthines | 1993 |
Structure-activity relationships at human and rat A2B adenosine receptors of xanthine derivatives substituted at the 1-, 3-, 7-, and 8-positions.
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 |
1-Isoamyl-3-isobutylxanthine: a remarkably potent agent for the potentiation of norepinephrine, histamine, and adenosine-elicited accumulations of cyclic AMP in brain slices.
Topics: 1-Methyl-3-isobutylxanthine; Adenosine; Animals; Brain; Cyclic AMP; Drug Synergism; Guinea Pigs; Histamine; In Vitro Techniques; Male; Norepinephrine; Phosphodiesterase Inhibitors; Theophylline; Xanthines | 1979 |
Stimulation by octopamine of the sodium efflux in barnacle muscle fibres.
Topics: 1-Methyl-3-isobutylxanthine; Animals; Calcium; Chlorphenamidine; In Vitro Techniques; Kinetics; Muscles; Octopamine; Ouabain; Sodium; Theophylline; Thoracica | 1984 |