Page last updated: 2024-09-03

omega-n-methylarginine and 1,3-dipropyl-8-cyclopentylxanthine

omega-n-methylarginine has been researched along with 1,3-dipropyl-8-cyclopentylxanthine in 5 studies

Compound Research Comparison

Studies
(omega-n-methylarginine)
Trials
(omega-n-methylarginine)
Recent Studies (post-2010)
(omega-n-methylarginine)
Studies
(1,3-dipropyl-8-cyclopentylxanthine)
Trials
(1,3-dipropyl-8-cyclopentylxanthine)
Recent Studies (post-2010) (1,3-dipropyl-8-cyclopentylxanthine)
4,4113443361,3011165

Protein Interaction Comparison

ProteinTaxonomyomega-n-methylarginine (IC50)1,3-dipropyl-8-cyclopentylxanthine (IC50)
Adenosine receptor A1Rattus norvegicus (Norway rat)0.0051
Adenosine receptor A3Rattus norvegicus (Norway rat)0.0038
Adenosine receptor A2aHomo sapiens (human)0.2033
Adenosine receptor A2bHomo sapiens (human)0.0234
Adenosine receptor A1Homo sapiens (human)0.0083

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Axe, FU; Bembenek, SD; Butler, CR; Coles, F; Dunford, PJ; Edwards, JP; Fourie, AM; Grice, CA; Karlsson, L; Lundeen, K; Riley, JP; Savall, BM; Tays, KL; Wei, J; Williams, KN; Xue, X1
Boegehold, MA; Sauls, BA1
Dennis, DM; Martynyuk, AE; Morey, TE; Rajasekaran, S1
Garrison, RN; Harris, PD; Li, N; Matheson, PJ; Zakaria, el R1
Althani, A; Fawzi, AA; Fituri, OM; Zakaria, el R1

Other Studies

5 other study(ies) available for omega-n-methylarginine and 1,3-dipropyl-8-cyclopentylxanthine

ArticleYear
Identification of a potent, selective, and orally active leukotriene a4 hydrolase inhibitor with anti-inflammatory activity.
    Journal of medicinal chemistry, 2008, Jul-24, Volume: 51, Issue:14

    Topics: Administration, Oral; Animals; Anti-Inflammatory Agents; Catalysis; Dogs; Drug Evaluation, Preclinical; Enzyme Inhibitors; Epoxide Hydrolases; Humans; Magnetic Resonance Spectroscopy; Mice; Structure-Activity Relationship

2008
Adenosine linking reduced O2 to arteriolar NO release in intestine is not formed from extracellular ATP.
    American journal of physiology. Heart and circulatory physiology, 2001, Volume: 281, Issue:3

    Topics: 5'-Nucleotidase; Adenosine; Adenosine Diphosphate; Adenosine Monophosphate; Adenosine Triphosphate; Animals; Arterioles; Enzyme Inhibitors; Extracellular Space; Intestine, Small; Male; Nitric Oxide; omega-N-Methylarginine; Oxygen; Rats; Rats, Sprague-Dawley; Vascular Patency; Vasoconstriction; Xanthines

2001
Free radicals potentiate the negative dromotropic effect of adenosine in guinea pig isolated heart.
    Acta cardiologica, 2003, Volume: 58, Issue:3

    Topics: Adenosine; Animals; Anti-Arrhythmia Agents; Atrioventricular Node; Bundle of His; Female; Free Radicals; Guinea Pigs; Heart; In Vitro Techniques; Male; Nitric Oxide; Nitric Oxide Synthase; omega-N-Methylarginine; Peroxynitrous Acid; Purinergic P1 Receptor Antagonists; Pyrogallol; Xanthines

2003
Glucose-induced intestinal vasodilation via adenosine A1 receptors requires nitric oxide but not K(+)(ATP) channels.
    The Journal of surgical research, 2011, Jun-15, Volume: 168, Issue:2

    Topics: Adenosine A1 Receptor Antagonists; Animals; Glucose; Glyburide; Hyperemia; Intestinal Absorption; Jejunum; KATP Channels; Male; Microscopy, Video; Microvessels; Nitric Oxide; Nitric Oxide Synthase; omega-N-Methylarginine; Rats; Rats, Sprague-Dawley; Receptor, Adenosine A1; Vasodilation; Xanthines

2011
Molecular mechanisms of peritoneal dialysis-induced microvascular vasodilation.
    Advances in peritoneal dialysis. Conference on Peritoneal Dialysis, 2014, Volume: 30

    Topics: Adenosine A1 Receptor Antagonists; Animals; Capillary Permeability; Dialysis Solutions; Diuretics, Osmotic; Endothelium, Vascular; Enzyme Inhibitors; Glucose; Glyburide; Hypoglycemic Agents; Ileum; Mannitol; Mefenamic Acid; omega-N-Methylarginine; Peritoneal Dialysis; Peritoneum; Rats; Vasodilation; Xanthines

2014