Page last updated: 2024-08-20

e-z cinnamic acid and 3,4-dihydroxyphenylpropionic acid

e-z cinnamic acid has been researched along with 3,4-dihydroxyphenylpropionic acid in 4 studies

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
Bora-Tatar, G; Dalkara, S; Dayangaç-Erden, D; Demir, AS; Erdem-Yurter, H; Yelekçi, K1
Aung, HT; Furukawa, T; Nikai, T; Niwa, M; Takaya, Y1
Blondel, A; Colas, C; Corringer, PJ; Delarue-Cochin, S; Joseph, D; Malliavin, T; Marteaux, J; Prevost, MS; Van Renterghem, C1
Allegretta, G; Empting, M; Hartmann, RW; Weidel, E1

Other Studies

4 other study(ies) available for e-z cinnamic acid and 3,4-dihydroxyphenylpropionic acid

ArticleYear
Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies.
    Bioorganic & medicinal chemistry, 2009, Jul-15, Volume: 17, Issue:14

    Topics: Caffeic Acids; Carboxylic Acids; Catalytic Domain; Chlorogenic Acid; Curcumin; Enzyme Inhibitors; HeLa Cells; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Models, Molecular; Molecular Structure; Protein Binding

2009
Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage.
    Bioorganic & medicinal chemistry, 2011, Apr-01, Volume: 19, Issue:7

    Topics: Animals; Antivenins; Caffeic Acids; Cinnamates; Crotalid Venoms; Depsides; Hemorrhage; Humans; Male; Mice; Rosmarinic Acid; Snakes; Structure-Activity Relationship

2011
Identification of cinnamic acid derivatives as novel antagonists of the prokaryotic proton-gated ion channel GLIC.
    Journal of medicinal chemistry, 2013, Jun-13, Volume: 56, Issue:11

    Topics: Animals; Bacterial Proteins; Binding Sites; Caffeic Acids; Cinnamates; Computer Simulation; Cyanobacteria; Databases, Factual; Female; Hydrogen-Ion Concentration; Ligand-Gated Ion Channels; Models, Molecular; Oocytes; Patch-Clamp Techniques; Protein Multimerization; Protons; Stereoisomerism; Xenopus

2013
Catechol-based substrates of chalcone synthase as a scaffold for novel inhibitors of PqsD.
    European journal of medicinal chemistry, 2015, Jan-27, Volume: 90

    Topics: Acyltransferases; Bacterial Proteins; Catechols; Enzyme Inhibitors; Pseudomonas aeruginosa; Quorum Sensing; Substrate Specificity

2015