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epigallocatechin gallate and naringin

epigallocatechin gallate has been researched along with naringin in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's4 (57.14)24.3611
2020's1 (14.29)2.80

Authors

AuthorsStudies
Backleh-Sohrt, M; Ekici, P; Leupold, G; Parlar, H1
Amić, D; Lucić, B1
Allen, JG; Babij, P; Fotsch, C1
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P1
Al-Asri, J; Fazekas, E; Görick, C; Gyémánt, G; Lehoczki, G; Melzig, MF; Mortier, J; Perdih, A; Wolber, G1
Fong, J; Korobkova, EA; Maran, U; Oja, M; Rice, M; Samuels, K; Sapse, AM; Williams, AK; Wong, B1
Hiratsuka, A; Nishimuta, H; Ogura, K; Ohtani, H; Sawada, Y; Tsujimoto, M1

Reviews

1 review(s) available for epigallocatechin gallate and naringin

ArticleYear
Emerging targets in osteoporosis disease modification.
    Journal of medicinal chemistry, 2010, Jun-10, Volume: 53, Issue:11

    Topics: Animals; Biomarkers; Bone Density; Bone Resorption; Humans; Osteoporosis

2010

Other Studies

6 other study(ies) available for epigallocatechin gallate and naringin

ArticleYear
Efficiency of foam fractionation for the enrichment of nonpolar compounds from aqueous extracts of plant materials.
    Journal of natural products, 2005, Volume: 68, Issue:9

    Topics: Carotenoids; Chemical Fractionation; Chromatography, High Pressure Liquid; Citrus; Curcuma; Curcumin; Cyclohexenes; Daucus carota; Flavanones; Hesperidin; Molecular Structure; Plant Extracts; Tea; Terpenes; Water

2005
Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids.
    Bioorganic & medicinal chemistry, 2010, Jan-01, Volume: 18, Issue:1

    Topics: Flavonoids; Free Radical Scavengers; Models, Biological; Quantitative Structure-Activity Relationship; Quantum Theory; Software; Thermodynamics

2010
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
    Bioorganic & medicinal chemistry, 2012, Nov-15, Volume: 20, Issue:22

    Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship

2012
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 role of flavonoids in cytochrome c-cardiolipin interactions.
    Bioorganic & medicinal chemistry, 2021, 03-01, Volume: 33

    Topics: Cardiolipins; Cytochromes c; Dose-Response Relationship, Drug; Enzyme Inhibitors; Flavonoids; Humans; Molecular Structure; Oxidation-Reduction; Structure-Activity Relationship

2021
Inhibitory effects of various beverages on human recombinant sulfotransferase isoforms SULT1A1 and SULT1A3.
    Biopharmaceutics & drug disposition, 2007, Volume: 28, Issue:9

    Topics: Adrenergic beta-Agonists; Arylsulfotransferase; Beverages; Biflavonoids; Biological Availability; Catechin; Citrus paradisi; Citrus sinensis; Flavanones; Flavones; Herb-Drug Interactions; Humans; In Vitro Techniques; Phenols; Polyphenols; Quercetin; Sulfotransferases; Tea

2007