Page last updated: 2024-09-04

8-chloroadenosine-3',5'-cyclic monophosphorothioate and probenecid

8-chloroadenosine-3',5'-cyclic monophosphorothioate has been researched along with probenecid in 1 studies

Compound Research Comparison

Studies
(8-chloroadenosine-3',5'-cyclic monophosphorothioate)
Trials
(8-chloroadenosine-3',5'-cyclic monophosphorothioate)
Recent Studies (post-2010)
(8-chloroadenosine-3',5'-cyclic monophosphorothioate)
Studies
(probenecid)
Trials
(probenecid)
Recent Studies (post-2010) (probenecid)
17013,664292375

Protein Interaction Comparison

ProteinTaxonomy8-chloroadenosine-3',5'-cyclic monophosphorothioate (IC50)probenecid (IC50)
Solute carrier family 22 member 8Mus musculus (house mouse)3.02
Solute carrier family 22 member 6Homo sapiens (human)6.85
Solute carrier family 22 member 8Homo sapiens (human)6.965
Solute carrier family 22 member 8Rattus norvegicus (Norway rat)6.03

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Christie, MJ; Hack, SP; Vaughan, CW1

Other Studies

1 other study(ies) available for 8-chloroadenosine-3',5'-cyclic monophosphorothioate and probenecid

ArticleYear
Modulation of GABA release during morphine withdrawal in midbrain neurons in vitro.
    Neuropharmacology, 2003, Volume: 45, Issue:5

    Topics: Action Potentials; Adenosine; Affinity Labels; Animals; Colforsin; Cyclic AMP; Dipyridamole; Dose-Response Relationship, Drug; Drug Interactions; Enkephalins; Enzyme Inhibitors; gamma-Aminobutyric Acid; In Vitro Techniques; Isoquinolines; Male; Mesencephalon; Mice; Mice, Inbred C57BL; Morphine; Morphine Dependence; Naloxone; Narcotic Antagonists; Narcotics; Neural Inhibition; Neurons; Patch-Clamp Techniques; Periaqueductal Gray; Probenecid; Purinergic P1 Receptor Agonists; Purinergic P1 Receptor Antagonists; Substance Withdrawal Syndrome; Sulfonamides; Synaptic Transmission; Thioinosine; Time Factors; Uricosuric Agents; Vasodilator Agents; Xanthines

2003