Page last updated: 2024-09-02

caffeic acid phenethyl ester and trans-4-coumaric acid

caffeic acid phenethyl ester has been researched along with trans-4-coumaric acid in 4 studies

Compound Research Comparison

Studies
(caffeic acid phenethyl ester)
Trials
(caffeic acid phenethyl ester)
Recent Studies (post-2010)
(caffeic acid phenethyl ester)
Studies
(trans-4-coumaric acid)
Trials
(trans-4-coumaric acid)
Recent Studies (post-2010) (trans-4-coumaric acid)
84014699554604

Protein Interaction Comparison

ProteinTaxonomycaffeic acid phenethyl ester (IC50)trans-4-coumaric acid (IC50)
TyrosinaseHomo sapiens (human)2.3333
Xanthine dehydrogenase/oxidaseBos taurus (cattle)6.8
large T antigenBetapolyomavirus macacae18.89

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
El-Kabbani, O; Endo, S; Hara, A; Hu, D; Ifuku, S; Li, J; Matsunaga, T; Ohta, S; Soda, M; Takemura, M; Toyooka, N; Wada, R; Yamamura, K; Zhao, HT1
El-Kabbani, O; Endo, S; Hara, A; Kanamori, A; Matsunaga, T; Nagai, H; Ohta, S; Otsuji, Y; Sundaram, K; Toyooka, N1
Borges, F; Mohamed, T; Rao, PPN; Remião, F; Shakeri, A; Silva, T; Soares da Silva, P1
Nishioka, N; Tsuji, T; Yoshizumi, K1

Other Studies

4 other study(ies) available for caffeic acid phenethyl ester and trans-4-coumaric acid

ArticleYear
Design, synthesis and evaluation of caffeic acid phenethyl ester-based inhibitors targeting a selectivity pocket in the active site of human aldo-keto reductase 1B10.
    European journal of medicinal chemistry, 2012, Volume: 48

    Topics: Aldehyde Reductase; Aldo-Keto Reductases; Antineoplastic Agents; Caffeic Acids; Catalytic Domain; Cell Survival; Enzyme Inhibitors; HeLa Cells; Humans; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Mass Spectrometry; Models, Molecular; Molecular Dynamics Simulation; Mutagenesis, Site-Directed; Propolis; Spectrophotometry, Infrared; Structure-Activity Relationship; U937 Cells

2012
Selective inhibition of human type-5 17β-hydroxysteroid dehydrogenase (AKR1C3) by baccharin, a component of Brazilian propolis.
    Journal of natural products, 2012, Apr-27, Volume: 75, Issue:4

    Topics: 3-Hydroxysteroid Dehydrogenases; Aldo-Keto Reductase Family 1 Member C3; Brazil; Crystallography, X-Ray; Humans; Hydroxyprostaglandin Dehydrogenases; Male; Molecular Conformation; Nuclear Magnetic Resonance, Biomolecular; Propolis; Stereoisomerism; Trichothecenes

2012
Repurposing nitrocatechols: 5-Nitro-α-cyanocarboxamide derivatives of caffeic acid and caffeic acid phenethyl ester effectively inhibit aggregation of tau-derived hexapeptide AcPHF6.
    European journal of medicinal chemistry, 2019, Apr-01, Volume: 167

    Topics: Caffeic Acids; Catechols; Chelating Agents; Copper; Drug Design; Nitro Compounds; Peptides; Phenylethyl Alcohol; Polyphenols; Protein Aggregation, Pathological; Small Molecule Libraries; tau Proteins; Tauopathies

2019
[Xanthine oxidase inhibitory activity and hypouricemia effect of propolis in rats].
    Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 2005, Volume: 125, Issue:3

    Topics: Animals; Anti-Infective Agents; Brazil; Caffeic Acids; China; Coumaric Acids; Disease Models, Animal; Flavonoids; Gout; Hyperuricemia; Male; Oxonic Acid; Phenylethyl Alcohol; Phenylpropionates; Propionates; Propolis; Rats; Rats, Sprague-Dawley; Uric Acid; Xanthine Oxidase

2005