beta-resorcylic acid has been researched along with protocatechuic acid in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (11.11) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (44.44) | 29.6817 |
2010's | 4 (44.44) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Günzler, V; Hanauske-Abel, HM; Kivirikko, KI; Majamaa, K; Myllylä, R | 1 |
Björnberg, O; Jensen, KF; Palfey, BA | 1 |
Fan, X; Lundell, D; Narula, S; Niu, X; Sun, J; Ting, P | 1 |
Jiang, L; Luo, WC; Xiao, T; Xie, XY; Xue, CB; Zhang, L | 1 |
Chesson, A; Duthie, GG; Russell, WR; Scobbie, L | 1 |
Cohen, SM; Fullagar, JL; Jacobsen, JA; Miller, MT | 1 |
Carta, F; Maresca, A; Scozzafava, A; Supuran, CT; Vullo, D | 1 |
Dong, MS; Hong, CY; Kim, IS; Kim, SA; Na, CS; Park, MH; Yoo, HH | 1 |
Brear, P; De Fusco, C; Georgiou, KH; Hyvönen, M; Iegre, J; Sore, HF; Spring, DR | 1 |
9 other study(ies) available for beta-resorcylic acid and protocatechuic acid
Article | Year |
---|---|
Partial identity of the 2-oxoglutarate and ascorbate binding sites of prolyl 4-hydroxylase.
Topics: Animals; Ascorbic Acid; Binding Sites; Chick Embryo; Ketoglutaric Acids; Kinetics; Phenols; Procollagen-Proline Dioxygenase; Protein Binding; Structure-Activity Relationship; Substrate Specificity | 1986 |
Specific inhibition of a family 1A dihydroorotate dehydrogenase by benzoate pyrimidine analogues.
Topics: Benzoates; Dihydroorotate Oxidase; Enzyme Inhibitors; Ligands; Pyrimidines; Structure-Activity Relationship; Trypanocidal Agents | 2001 |
Inhibition of fucosyltransferase VII by gallic acid and its derivatives.
Topics: Catechin; Ellagic Acid; Enzymes; Fucosyltransferases; Gallic Acid; Humans; Manganese | 2004 |
3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.
Topics: Benzaldehydes; Benzoic Acid; Enzyme Inhibitors; Hydrogen Bonding; Models, Molecular; Monophenol Monooxygenase; Quantitative Structure-Activity Relationship; Thiosemicarbazones | 2007 |
Inhibition of 15-lipoxygenase-catalysed oxygenation of arachidonic acid by substituted benzoic acids.
Topics: Arachidonate 15-Lipoxygenase; Arachidonic Acid; Benzoates; Catalysis; Colon; Enzyme Inhibitors; Humans; Lipoxygenase Inhibitors; Oxidation-Reduction; Oxygen; Structure-Activity Relationship | 2008 |
Identifying chelators for metalloprotein inhibitors using a fragment-based approach.
Topics: Antigens, Bacterial; Bacterial Toxins; Chelating Agents; Copper; Drug Design; Humans; Hydroxyquinolines; Iron; Ligands; Lipoxygenase Inhibitors; Matrix Metalloproteinase Inhibitors; Matrix Metalloproteinases; Monophenol Monooxygenase; Nitric Oxide Synthase Type II; Recombinant Proteins; Small Molecule Libraries; Structure-Activity Relationship; Sulfonamides; Zinc | 2011 |
Mono-/dihydroxybenzoic acid esters and phenol pyridinium derivatives as inhibitors of the mammalian carbonic anhydrase isoforms I, II, VII, IX, XII and XIV.
Topics: Animals; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Esters; Hydroxybenzoates; Isoenzymes; Kinetics; Phenol; Protein Binding; Pyridinium Compounds; Structure-Activity Relationship | 2013 |
Inhibitory effect of Rhus verniciflua Stokes extract on human aromatase activity; butin is its major bioactive component.
Topics: Aromatase; Aromatase Inhibitors; Benzopyrans; Dose-Response Relationship, Drug; Humans; Medicine, Traditional; Molecular Structure; Plant Extracts; Plant Structures; Rhus; Structure-Activity Relationship | 2014 |
A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066.
Topics: Binding Sites; Biphenyl Compounds; Casein Kinase II; Crystallography, X-Ray; Dose-Response Relationship, Drug; Drug Discovery; Humans; Models, Molecular; Molecular Structure; Protein Kinase Inhibitors; Structure-Activity Relationship | 2017 |