Compounds > catechol

catechol and luteolin

catechol has been researched along with luteolin in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (42.86)	29.6817
2010's	3 (42.86)	24.3611
2020's	1 (14.29)	2.80

Authors

Authors	Studies
Bellows, DS; Clarke, ID; Diamandis, P; Dirks, PB; Graham, J; Jamieson, LG; Ling, EK; Sacher, AG; Tyers, M; Ward, RJ; Wildenhain, J	1
Ekinci, D; Karagoz, L; Senturk, M; Supuran, CT	1
Bücherl, D; Decker, M; Heilmann, J; Kling, B; Matysik, FM; Palatzky, P; Wegener, J	1
Kalra, S; Khatik, GL; Kumar, GN; Kumar, R; Narang, R; Nayak, SK; Singh, SK; Sudhakar, K	1
Boersma, MG; Gliszczyńska-Swigło, A; Lemańska, K; Rietjens, IM; Szymusiak, H; Tyrakowska, B; van der Woude, H	1
Murakami, S; Shiraiwa, M; Takahara, H	1
Arroo, R; Cao, H; Högger, P; Xiao, J	1

Reviews

1 review(s) available for catechol and luteolin

Article	Year
Recent advancements in mechanistic studies and structure activity relationship of F European journal of medicinal chemistry, 2019, Nov-15, Volume: 182 Topics: Animals; Anti-Bacterial Agents; Dose-Response Relationship, Drug; Enzyme Inhibitors; Humans; Microbial Sensitivity Tests; Molecular Structure; Mycobacterium; Proton-Translocating ATPases; Structure-Activity Relationship	2019

Other Studies

6 other study(ies) available for catechol and luteolin

Article	Year
Chemical genetics reveals a complex functional ground state of neural stem cells. Nature chemical biology, 2007, Volume: 3, Issue:5 Topics: Animals; Cell Survival; Cells, Cultured; Mice; Molecular Structure; Neoplasms; Neurons; Pharmaceutical Preparations; Sensitivity and Specificity; Stem Cells	2007
Carbonic anhydrase inhibitors: in vitro inhibition of α isoforms (hCA I, hCA II, bCA III, hCA IV) by flavonoids. Journal of enzyme inhibition and medicinal chemistry, 2013, Volume: 28, Issue:2 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Flavonoids; Humans; Molecular Structure; Protein Isoforms; Structure-Activity Relationship	2013
Flavonoids, flavonoid metabolites, and phenolic acids inhibit oxidative stress in the neuronal cell line HT-22 monitored by ECIS and MTT assay: a comparative study. Journal of natural products, 2014, Mar-28, Volume: 77, Issue:3 Topics: Animals; Cells, Cultured; Dose-Response Relationship, Drug; Flavonoids; Hippocampus; Hydroxybenzoates; Mice; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Oxidative Stress; Quercetin	2014
The effect of catechol O-methylation on radical scavenging characteristics of quercetin and luteolin--a mechanistic insight. Free radical research, 2004, Volume: 38, Issue:6 Topics: Antioxidants; Apigenin; Catechols; Flavonoids; Free Radical Scavengers; Hydrogen; Hydrogen-Ion Concentration; Kaempferols; Luteolin; Methylation; Molecular Structure; Quercetin	2004
Purification and characterization of three neutral extracellular isoperoxidases from rye leaves. Phytochemistry, 2007, Volume: 68, Issue:6 Topics: Catechols; Chromatography, High Pressure Liquid; Cresols; Electrophoresis; Glucuronides; Guaiacol; Hydrogen Peroxide; Hydrogen-Ion Concentration; Isoelectric Point; Isoenzymes; Luteolin; Molecular Structure; Molecular Weight; Peroxidases; Plant Leaves; Plant Proteins; Secale; Substrate Specificity; Temperature	2007
Flavonols with a catechol or pyrogallol substitution pattern on ring B readily form stable dimers in phosphate buffered saline at four degrees celsius. Food chemistry, 2020, May-01, Volume: 311 Topics: Buffers; Catechols; Cold Temperature; Dimerization; Flavanones; Flavonoids; Flavonols; Kaempferols; Luteolin; Molecular Structure; Oxidation-Reduction; Phosphates; Pyrogallol; Quercetin	2020