Compounds > 2,3-dihydroxybenzoic acid

2,3-dihydroxybenzoic acid and 3,4-dihydroxyphenylpropionic acid

2,3-dihydroxybenzoic acid has been researched along with 3,4-dihydroxyphenylpropionic acid in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Günzler, V; Hanauske-Abel, HM; Kivirikko, KI; Majamaa, K; Myllylä, R1
Bora-Tatar, G; Dalkara, S; Dayangaç-Erden, D; Demir, AS; Erdem-Yurter, H; Yelekçi, K1
Al-Asri, J; Fazekas, E; Görick, C; Gyémánt, G; Lehoczki, G; Melzig, MF; Mortier, J; Perdih, A; Wolber, G1
Aoki, R; Asakura, T; Ezcurra, M; Goshima, Y; Ibi, M; Iino, Y; Kajihara, Y; Kanai, Y; Misu, Y; Miyamae, T; Mori, I; Nakamura, F; Ogura, K; Sasakura, H; Schafer, WR; Yagami, T1

Other Studies

4 other study(ies) available for 2,3-dihydroxybenzoic acid and 3,4-dihydroxyphenylpropionic acid

ArticleYear
Partial identity of the 2-oxoglutarate and ascorbate binding sites of prolyl 4-hydroxylase.
    The Journal of biological chemistry, 1986, Jun-15, Volume: 261, Issue:17

    Topics: Animals; Ascorbic Acid; Binding Sites; Chick Embryo; Ketoglutaric Acids; Kinetics; Phenols; Procollagen-Proline Dioxygenase; Protein Binding; Structure-Activity Relationship; Substrate Specificity

1986
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
From carbohydrates to drug-like fragments: Rational development of novel α-amylase inhibitors.
    Bioorganic & medicinal chemistry, 2015, Oct-15, Volume: 23, Issue:20

    Topics: alpha-Amylases; Carbohydrates; Dose-Response Relationship, Drug; Drug Discovery; Enzyme Inhibitors; High-Throughput Screening Assays; Humans; Models, Molecular; Molecular Structure; Structure-Activity Relationship

2015
A seven-transmembrane receptor that mediates avoidance response to dihydrocaffeic acid, a water-soluble repellent in Caenorhabditis elegans.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011, Nov-16, Volume: 31, Issue:46

    Topics: 3,4-Dihydroxyphenylacetic Acid; Analysis of Variance; Animals; Animals, Genetically Modified; Behavior, Animal; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Caffeic Acids; Catechols; Cloning, Molecular; Dose-Response Relationship, Drug; Escape Reaction; Hydroxybenzoates; Larva; Luminescent Proteins; Membrane Potentials; Microinjections; Models, Molecular; Mutation; Receptors, G-Protein-Coupled; Sensory Receptor Cells; Xenopus

2011