Page last updated: 2024-09-02

caffeic acid phenethyl ester and loxapine

caffeic acid phenethyl ester has been researched along with loxapine 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
(loxapine)
Trials
(loxapine)
Recent Studies (post-2010) (loxapine)
840146936371104

Protein Interaction Comparison

ProteinTaxonomycaffeic acid phenethyl ester (IC50)loxapine (IC50)
5-hydroxytryptamine receptor 2CRattus norvegicus (Norway rat)1
Muscarinic acetylcholine receptor M1Homo sapiens (human)5.5
D(2) dopamine receptorHomo sapiens (human)0.054
Alpha-1B adrenergic receptorRattus norvegicus (Norway rat)0.018
D(4) dopamine receptorHomo sapiens (human)0.014
Alpha-1D adrenergic receptorRattus norvegicus (Norway rat)0.018
Histamine H1 receptorRattus norvegicus (Norway rat)1
D(3) dopamine receptorHomo sapiens (human)0.022
Alpha-1A adrenergic receptorRattus norvegicus (Norway rat)0.018

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 loxapine

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