Page last updated: 2024-09-02

caffeic acid phenethyl ester and 2-Phenylethyl 3-phenyl-2-propenoate

caffeic acid phenethyl ester has been researched along with 2-Phenylethyl 3-phenyl-2-propenoate in 6 studies

Compound Research Comparison

Studies
(caffeic acid phenethyl ester)
Trials
(caffeic acid phenethyl ester)
Recent Studies (post-2010)
(caffeic acid phenethyl ester)
Studies
(2-Phenylethyl 3-phenyl-2-propenoate)
Trials
(2-Phenylethyl 3-phenyl-2-propenoate)
Recent Studies (post-2010) (2-Phenylethyl 3-phenyl-2-propenoate)
84014691007

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (100.00)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
Choi, HJ; Chung, TW; Ha, KT; Jeong, HS; Kim, CH; Lee, JY1
Han, MS; Kim, DW; Lee, IK; Yun, BS1
Kosaka, Y; Mizuguchi, M; Yokoyama, T1
Endo, Y; Hatayama, K; Hayashi, T; Nakano, H; Ohta, K; Sato, D; Sato, Y; Seki, C; Taguchi, R; Takahashi, T; Tokuraku, K; Uwai, K1
Csuk, R; Gießel, JM; Loesche, A; Serbian, I1

Other Studies

6 other study(ies) available for caffeic acid phenethyl ester and 2-Phenylethyl 3-phenyl-2-propenoate

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
Caffeic acid phenethyl ester inhibits alpha-melanocyte stimulating hormone-induced melanin synthesis through suppressing transactivation activity of microphthalmia-associated transcription factor.
    Journal of natural products, 2013, Aug-23, Volume: 76, Issue:8

    Topics: alpha-MSH; Animals; Blotting, Western; Caffeic Acids; Cyclic AMP Response Element-Binding Protein; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; Interferon Type I; Intramolecular Oxidoreductases; Levodopa; Melanins; Mice; Microphthalmia-Associated Transcription Factor; Molecular Structure; Monophenol Monooxygenase; Oxidoreductases; Phenylethyl Alcohol; Pregnancy Proteins; Transcriptional Activation

2013
Phenylpropanoid acid esters from Korean propolis and their antioxidant activities.
    Bioorganic & medicinal chemistry letters, 2014, Aug-01, Volume: 24, Issue:15

    Topics: Antioxidants; Coumaric Acids; DNA Damage; Esters; Molecular Structure; Propolis; Republic of Korea

2014
Inhibitory activities of propolis and its promising component, caffeic acid phenethyl ester, against amyloidogenesis of human transthyretin.
    Journal of medicinal chemistry, 2014, Nov-13, Volume: 57, Issue:21

    Topics: Amyloid Neuropathies, Familial; Amyloidosis; Caffeic Acids; Coumaric Acids; Masoprocol; Phenylethyl Alcohol; Prealbumin; Propolis

2014
Structure-activity relations of rosmarinic acid derivatives for the amyloid β aggregation inhibition and antioxidant properties.
    European journal of medicinal chemistry, 2017, Sep-29, Volume: 138

    Topics: Amyloid beta-Peptides; Antioxidants; Cinnamates; Depsides; Dose-Response Relationship, Drug; Humans; Molecular Dynamics Simulation; Molecular Structure; Protein Aggregates; Rosmarinic Acid; Structure-Activity Relationship

2017
Caffeic acid phenethyl ester (CAPE)-derivatives act as selective inhibitors of acetylcholinesterase.
    European journal of medicinal chemistry, 2019, Sep-01, Volume: 177

    Topics: Acetylcholinesterase; Animals; Butyrylcholinesterase; Caffeic Acids; Catalytic Domain; Cell Line, Tumor; Cholinesterase Inhibitors; Electrophorus; Horses; Humans; Mice; Molecular Docking Simulation; NIH 3T3 Cells; Phenylethyl Alcohol

2019