Page last updated: 2024-09-02

r 56865 and bepridil

r 56865 has been researched along with bepridil in 1 studies

Compound Research Comparison

Studies
(r 56865)
Trials
(r 56865)
Recent Studies (post-2010)
(r 56865)
Studies
(bepridil)
Trials
(bepridil)
Recent Studies (post-2010) (bepridil)
72107987094

Protein Interaction Comparison

ProteinTaxonomyr 56865 (IC50)bepridil (IC50)
Voltage-dependent L-type calcium channel subunit alpha-1CCavia porcellus (domestic guinea pig)1.4
Voltage-dependent L-type calcium channel subunit alpha-1FHomo sapiens (human)1
Lethal factorBacillus anthracis4.8
Voltage-dependent L-type calcium channel subunit alpha-1D Homo sapiens (human)1
Potassium voltage-gated channel subfamily H member 2Homo sapiens (human)0.5184
Voltage-dependent L-type calcium channel subunit alpha-1SHomo sapiens (human)1
Voltage-dependent L-type calcium channel subunit alpha-1CHomo sapiens (human)1.2
Sodium channel protein type 5 subunit alphaHomo sapiens (human)3.7

Research

Studies (1)

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

Authors

AuthorsStudies
Arita, M; Li, Y; Sato, T1

Other Studies

1 other study(ies) available for r 56865 and bepridil

ArticleYear
Bepridil blunts the shortening of action potential duration caused by metabolic inhibition via blockade of ATP-sensitive K(+) channels and Na(+)-activated K(+) channels.
    The Journal of pharmacology and experimental therapeutics, 1999, Volume: 291, Issue:2

    Topics: Action Potentials; Adenosine Triphosphate; Animals; Anti-Arrhythmia Agents; Benzothiazoles; Bepridil; Calcium Channel Blockers; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Dose-Response Relationship, Drug; Glyburide; Guinea Pigs; Heart Ventricles; In Vitro Techniques; Patch-Clamp Techniques; Perfusion; Piperidines; Potassium Channels; Sodium; Thiazoles; Time Factors; Uncoupling Agents

1999