1,3-dipropyl-8-cyclopentylxanthine has been researched along with peoniflorin in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (33.33) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cheng, JT; Hsu, FL; Lai, CW | 1 |
Cheng, JT; Hsu, FL; Wang, CJ | 1 |
Matsumoto, K; Murakami, Y; Tabata, K; Watanabe, H | 1 |
Cheng, JT; Liu, IM; Tang, LM | 1 |
Ji, XQ; Jiang, CL; Liu, DZ; Xie, KQ; Ye, Y; Zhu, XZ | 1 |
Hu, J; Huo, X; Li, J; Liu, Q; Ma, S; Sun, J; Sun, L; Wang, H; Zhao, M | 1 |
6 other study(ies) available for 1,3-dipropyl-8-cyclopentylxanthine and peoniflorin
Article | Year |
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Stimulatory effect of paeoniflorin on adenosine A-1 receptors to increase the translocation of protein kinase C (PKC) and glucose transporter (GLUT 4) in isolated rat white adipocytes.
Topics: Adipocytes; Alkaloids; Animals; Anti-Inflammatory Agents, Non-Steroidal; Benzoates; Benzophenanthridines; Bridged-Ring Compounds; Cell Membrane; Cytosol; Drug Interactions; Enzyme Inhibitors; Glucose Transporter Type 4; Glucosides; Isoenzymes; Monosaccharide Transport Proteins; Monoterpenes; Muscle Proteins; Phenanthridines; Phosphorylation; Protein Kinase C; Protein Kinase C beta; Purinergic P1 Receptor Agonists; Rats; Rats, Wistar; Signal Transduction; Stimulation, Chemical; Xanthines | 1998 |
Paeoniflorin reverses guanethidine-induced hypotension via activation of central adenosine A1 receptors in Wistar rats.
Topics: Adrenergic Agents; Animals; Anti-Inflammatory Agents, Non-Steroidal; Benzoates; Blood Pressure; Bridged-Ring Compounds; Dose-Response Relationship, Drug; Glucosides; Guanethidine; Hypotension; Male; Monoterpenes; Plants, Medicinal; Purinergic P1 Receptor Antagonists; Rats; Rats, Wistar; Receptors, Purinergic P1; Xanthines | 1999 |
Ameliorative effects of paeoniflorin, a major constituent of peony root, on adenosine A1 receptor-mediated impairment of passive avoidance performance and long-term potentiation in the hippocampus.
Topics: Adenosine; Animals; Avoidance Learning; Benzoates; Bridged-Ring Compounds; Glucosides; Hippocampus; Long-Term Potentiation; Male; Mice; Monoterpenes; Rats; Rats, Wistar; Receptors, Purinergic P1; Xanthines | 2001 |
Stimulatory effect of paeoniflorin on adenosine release to increase the glucose uptake into white adipocytes of Wistar rat.
Topics: Adenosine; Adipocytes; Animals; Benzoates; Bridged-Ring Compounds; Carbon Radioisotopes; Deoxyglucose; Dose-Response Relationship, Drug; Glucose; Glucosides; Male; Monoterpenes; Paeonia; Phytotherapy; Plant Extracts; Rats; Rats, Wistar; Xanthines | 2003 |
Neuroprotective effect of paeoniflorin on cerebral ischemic rat by activating adenosine A1 receptor in a manner different from its classical agonists.
Topics: Adenosine-5'-(N-ethylcarboxamide); Animals; Benzoates; Binding, Competitive; Bridged-Ring Compounds; Cerebral Cortex; Disease Models, Animal; Dose-Response Relationship, Drug; Glucosides; Infarction, Middle Cerebral Artery; Inhibitory Concentration 50; Ischemic Attack, Transient; Male; Monoterpenes; Neuroprotective Agents; Paeonia; Plant Roots; Rats; Rats, Sprague-Dawley; Receptor, Adenosine A1; Time Factors; Xanthines | 2005 |
ADAM17 participates in the protective effect of paeoniflorin on mouse brain microvascular endothelial cells.
Topics: ADAM17 Protein; Animals; Brain; Cell Line; Cell Membrane; Cell Survival; Endothelial Cells; ErbB Receptors; Glucosides; Hydrogen Peroxide; Mice; Microvessels; Models, Biological; Monoterpenes; Neuroprotective Agents; Phosphorylation; Receptor, Adenosine A1; Receptors, Tumor Necrosis Factor, Type I; Signal Transduction; Solubility; src-Family Kinases; Transcriptional Activation; Xanthines | 2018 |