3,7-dimethyl-1-propargylxanthine has been researched along with Ache in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Choi, SS; Han, EJ; Han, KJ; Kim, DH; Lee, HK; Lee, JK; Suh, HW | 1 |
| Malec, D; Poleszak, E | 1 |
| Doak, GJ; Reid, AR; Sawynok, J; Zarrindast, MR | 1 |
| Poon, A; Sawynok, J | 1 |
4 other study(ies) available for 3,7-dimethyl-1-propargylxanthine and Ache
| Article | Year |
|---|---|
Antinociceptive mechanisms of orally administered decursinol in the mouse.
Topics: Administration, Oral; Adrenergic alpha-Antagonists; Analgesics; Animals; Benzopyrans; Butyrates; Cyproheptadine; Dose-Response Relationship, Drug; Glutamic Acid; Histamine H2 Antagonists; Interferon-gamma; Interleukin-1; Male; Methysergide; Mice; Mice, Inbred ICR; Models, Chemical; Naloxone; Narcotic Antagonists; Pain; Piperidines; Protein Kinase C; Ranitidine; Receptors, Adrenergic; Receptors, Histamine; Receptors, Purinergic P1; Receptors, Serotonin; Serotonin Antagonists; Substance P; Theobromine; Tumor Necrosis Factor-alpha; Xanthines; Yohimbine | 2003 |
Adenosine receptor ligands and dizocilpine-induced antinociception in mice.
Topics: Acetic Acid; Animals; Behavior, Animal; Dizocilpine Maleate; Excitatory Amino Acid Antagonists; Male; Mice; Nociceptors; Pain; Purinergic P1 Receptor Agonists; Receptors, Purinergic P1; Theobromine; Xanthines | 2005 |
Adenosine A3 receptor activation produces nociceptive behaviour and edema by release of histamine and 5-hydroxytryptamine.
Topics: Animals; Behavior, Animal; Body Temperature; Edema; Histamine Release; Injections, Subcutaneous; Male; Pain; Plethysmography; Rats; Rats, Sprague-Dawley; Receptors, Purinergic P1; Serotonin; Theobromine; Theophylline | 1997 |
Antinociceptive and anti-inflammatory properties of an adenosine kinase inhibitor and an adenosine deaminase inhibitor.
Topics: Adenosine Deaminase; Adenosine Deaminase Inhibitors; Adenosine Kinase; Analgesics; Animals; Anti-Inflammatory Agents; Caffeine; Carrageenan; Central Nervous System Stimulants; Deoxyadenosines; Dose-Response Relationship, Drug; Drug Synergism; Edema; Enzyme Inhibitors; Hindlimb; Hyperalgesia; Injections, Spinal; Male; Nociceptors; Pain; Pentostatin; Proto-Oncogene Proteins c-fos; Purinergic P1 Receptor Antagonists; Rats; Rats, Sprague-Dawley; Spinal Cord; Theobromine; Time Factors | 1999 |