Page last updated: 2024-09-02

caffeic acid phenethyl ester and amlodipine

caffeic acid phenethyl ester has been researched along with amlodipine in 1 studies

Compound Research Comparison

Studies
(caffeic acid phenethyl ester)
Trials
(caffeic acid phenethyl ester)
Recent Studies (post-2010)
(caffeic acid phenethyl ester)
Studies
(amlodipine)
Trials
(amlodipine)
Recent Studies (post-2010) (amlodipine)
84014694,2001,5041,671

Protein Interaction Comparison

ProteinTaxonomycaffeic acid phenethyl ester (IC50)amlodipine (IC50)
Voltage-dependent L-type calcium channel subunit alpha-1CCavia porcellus (domestic guinea pig)1.2
Potassium channel subfamily K member 2Homo sapiens (human)0.4
Alpha-2A adrenergic receptorHomo sapiens (human)0.602
Alpha-2C adrenergic receptorHomo sapiens (human)1.8
5-hydroxytryptamine receptor 6Homo sapiens (human)2.898
Sodium-dependent dopamine transporter Homo sapiens (human)5.521
Voltage-dependent L-type calcium channel subunit alpha-1CHomo sapiens (human)2.7
Potassium channel subfamily K member 2 Bos taurus (cattle)0.43

Research

Studies (1)

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

Authors

AuthorsStudies
Bennis, K; Ducki, S; Lesage, F; Vivier, D1

Reviews

1 review(s) available for caffeic acid phenethyl ester and amlodipine

ArticleYear
Perspectives on the Two-Pore Domain Potassium Channel TREK-1 (TWIK-Related K(+) Channel 1). A Novel Therapeutic Target?
    Journal of medicinal chemistry, 2016, 06-09, Volume: 59, Issue:11

    Topics: Arrhythmias, Cardiac; Depression; Epilepsy; Humans; Inflammation; Models, Molecular; Molecular Structure; Neuroprotective Agents; Pain; Potassium Channels, Tandem Pore Domain; Structure-Activity Relationship

2016