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3,7-dimethyl-1-propargylxanthine and Edema

3,7-dimethyl-1-propargylxanthine has been researched along with Edema in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (50.00)18.2507
2000's2 (33.33)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gong, ZH; Huang, B; Jia, YX; Su, RB; Wang, ML; Wang, ZT; Yi, SP; Yu, G; Zhang, FY1
Castellino, AJ; DaRe, JS; Erion, MD; Kopcho, JJ; Ramirez-Weinhouse, M; Rosengren, S; Ugarkar, BG1
Doak, GJ; Reid, AR; Sawynok, J; Zarrindast, MR1
Besson, JM; Buritova, J; Chapman, V; Honoré, P1
Poon, A; Sawynok, J1
Masamune, A; Satoh, A; Satoh, K; Shimosegawa, T; Yamagiwa, T1

Other Studies

6 other study(ies) available for 3,7-dimethyl-1-propargylxanthine and Edema

ArticleYear
Antinociceptive effects of incarvillateine, a monoterpene alkaloid from Incarvillea sinensis, and possible involvement of the adenosine system.
    Scientific reports, 2015, Nov-03, Volume: 5

    Topics: Adenosine; Alkaloids; Analgesics; Animals; Antineoplastic Agents, Phytogenic; Bignoniaceae; Disease Models, Animal; Edema; Freund's Adjuvant; Hyperalgesia; Interleukin-1beta; Medicine, Chinese Traditional; Mice; Monoterpenes; Motor Activity; Paclitaxel; Pain Measurement; Theobromine; Theophylline; Xanthines

2015
Adenosine kinase inhibitors. 3. Synthesis, SAR, and antiinflammatory activity of a series of l-lyxofuranosyl nucleosides.
    Journal of medicinal chemistry, 2003, Oct-23, Volume: 46, Issue:22

    Topics: Adenosine Kinase; Animals; Anti-Inflammatory Agents, Non-Steroidal; Dose-Response Relationship, Drug; Edema; Leukocyte Count; Neutrophils; Nucleosides; Phosphorylation; Purinergic P1 Receptor Antagonists; Rats; Skin; Structure-Activity Relationship; Theobromine

2003
Adenosine A3 receptor activation produces nociceptive behaviour and edema by release of histamine and 5-hydroxytryptamine.
    European journal of pharmacology, 1997, Aug-20, Volume: 333, Issue:1

    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
UP 202-56, an adenosine analogue, selectively acts via A1 receptors to significantly decrease noxiously-evoked spinal c-Fos protein expression.
    Pain, 1998, Volume: 75, Issue:2-3

    Topics: Adenosine; Administration, Oral; Animals; Carrageenan; Edema; Hindlimb; Indoles; Male; Proto-Oncogene Proteins c-fos; Purines; Rats; Rats, Sprague-Dawley; Receptors, Purinergic P1; Spinal Cord; Theobromine; Xanthines

1998
Antinociceptive and anti-inflammatory properties of an adenosine kinase inhibitor and an adenosine deaminase inhibitor.
    European journal of pharmacology, 1999, Nov-19, Volume: 384, Issue:2-3

    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
Activation of adenosine A2a receptor pathway reduces leukocyte infiltration but enhances edema formation in rat caerulein pancreatitis.
    Pancreas, 2002, Volume: 24, Issue:1

    Topics: Adenosine; Amylases; Animals; Ceruletide; Edema; Leukocytes; Male; Pancreatitis; Phenethylamines; Purinergic P1 Receptor Agonists; Purinergic P1 Receptor Antagonists; Rats; Rats, Wistar; Receptors, Purinergic P1; Theobromine

2002