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resveratrol and 3,5,4'-trihydroxystilbene-4'-o-glucoside

resveratrol has been researched along with 3,5,4'-trihydroxystilbene-4'-o-glucoside in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's5 (83.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ashendel, CL; Chang, CJ; Geahlen, RL; Jayasuriya, H; Jayatilake, GS; Koonchanok, NM; Lee, ES; McLaughlin, JL1
Amira-Guebalia, H; Andriamanarivo, S; Delaunay, JC; Delchier, N; Fortin, PY; Kapche, GD; Mérillon, JM; Monti, JP; Papastamoulis, Y; Richard, T; Rivière, C; Waffo-Teguo, P1
Alcántara, D; Beltrán, D; Espín, JC; García-Conesa, MT; Larrosa, M; Lucas, R; Morales, JC; Selma, MV; Tomás-Barberán, F; Tomé-Carneiro, J; Urbán, C; Yáñez-Gascón, MJ1
Kohl, R; Mayr, F; Moesslacher, J; Pagitz, K; Rainer, B; Revoltella, S; Scalfari, V; Schwaiger, S; Siewert, B; Stuppner, H; Waltenberger, B1
Mikulski, D; Molski, M1
Hamada, H; Imai, H; Ishihara, K; Kitagawa, M; Masuoka, N; Nakajima, N; Shimoda, K1

Other Studies

6 other study(ies) available for resveratrol and 3,5,4'-trihydroxystilbene-4'-o-glucoside

ArticleYear
Kinase inhibitors from Polygonum cuspidatum.
    Journal of natural products, 1993, Volume: 56, Issue:10

    Topics: Animals; Cattle; Magnetic Resonance Spectroscopy; Medicine, Chinese Traditional; Plants, Medicinal; Protein-Tyrosine Kinases; Rats; Resveratrol; Spectrophotometry, Ultraviolet; Stereoisomerism; Stilbenes; Thymus Gland

1993
New stilbene dimers against amyloid fibril formation.
    Bioorganic & medicinal chemistry letters, 2010, Jun-01, Volume: 20, Issue:11

    Topics: Amyloid; Dimerization; Stilbenes

2010
Preventive oral treatment with resveratrol pro-prodrugs drastically reduce colon inflammation in rodents.
    Journal of medicinal chemistry, 2010, Oct-28, Volume: 53, Issue:20

    Topics: Acute-Phase Proteins; Administration, Oral; Animals; Anti-Inflammatory Agents, Non-Steroidal; Cell Line; Colitis; Colon; Cytokines; Dextran Sulfate; Diarrhea; Dinoprostone; Feces; Gastrointestinal Transit; Glucosides; Humans; Intestinal Absorption; Intestinal Mucosa; Mice; Mice, Inbred C57BL; Peroxidase; Prodrugs; Resveratrol; Stereoisomerism; Stilbenes; Structure-Activity Relationship

2010
From bench to counter: Discovery and validation of a peony extract as tyrosinase inhibiting cosmeceutical.
    European journal of medicinal chemistry, 2019, Dec-15, Volume: 184

    Topics: Adult; Agaricales; Aged; Animals; Cell Line, Tumor; Cell Survival; Cosmeceuticals; Dose-Response Relationship, Drug; Drug Discovery; Female; Humans; Light; Male; Mice; Middle Aged; Molecular Structure; Monophenol Monooxygenase; Paeonia; Plant Extracts; Seeds; Skin; Structure-Activity Relationship

2019
Quantitative structure-antioxidant activity relationship of trans-resveratrol oligomers, trans-4,4'-dihydroxystilbene dimer, trans-resveratrol-3-O-glucuronide, glucosides: trans-piceid, cis-piceid, trans-astringin and trans-resveratrol-4'-O-beta-D-glucopy
    European journal of medicinal chemistry, 2010, Volume: 45, Issue:6

    Topics: Dimerization; Free Radical Scavengers; Glucose; Glucosides; Glucuronides; Models, Molecular; Molecular Conformation; Quantitative Structure-Activity Relationship; Quantum Theory; Resveratrol; Stereoisomerism; Stilbenes

2010
Glycosylation of trans-resveratrol by plant-cultured cells.
    Bioscience, biotechnology, and biochemistry, 2012, Volume: 76, Issue:8

    Topics: Biotransformation; Catharanthus; Cells, Cultured; Glucose; Glucosides; Glycosides; Glycosylation; Ipomoea batatas; Molecular Structure; Plant Cells; Resveratrol; Stereoisomerism; Stilbenes; Strophanthus

2012