resveratrol has been researched along with 3,4,4'-trihydroxy-trans-stilbene in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cushman, M; Geahlen, RL; Thakkar, K | 1 |
Croy, VL; Cuendet, M; Endringer, DC; Kang, SS; Lipton, MA; Pezzuto, JM | 1 |
Cai, YJ; Fan, GJ; Fang, JG; Li, XZ; Qian, YP; Wei, QY; Yang, J; Zheng, LF; Zhou, B | 1 |
Calamini, B; Chen, Y; Jensen, KC; Kang, S; Lipton, MA; Mesecar, AD; St John, SE | 1 |
Nakanishi, I; Sekine-Suzuki, E; Sonoda, M; Tanimori, S; Uzura, S | 1 |
Dai, Y; Kogure, Y; Mabuchi, M; Nakao, S; Noguchi, K; Shimizu, T; Tanaka, A; Wang, S | 1 |
6 other study(ies) available for resveratrol and 3,4,4'-trihydroxy-trans-stilbene
Article | Year |
---|---|
Synthesis and protein-tyrosine kinase inhibitory activity of polyhydroxylated stilbene analogues of piceatannol.
Topics: Hydroxylation; Lymphocyte Specific Protein Tyrosine Kinase p56(lck); Lymphocytes; Molecular Structure; Phenols; Protein-Tyrosine Kinases; Stilbenes; Structure-Activity Relationship | 1993 |
Synthesis and biological evaluation of a library of resveratrol analogues as inhibitors of COX-1, COX-2 and NF-kappaB.
Topics: Antioxidants; Cell Line; Combinatorial Chemistry Techniques; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Humans; Inhibitory Concentration 50; NF-kappa B; Resveratrol; Small Molecule Libraries; Stilbenes; Structure-Activity Relationship | 2009 |
Antioxidant-based lead discovery for cancer chemoprevention: the case of resveratrol.
Topics: Animals; Anticarcinogenic Agents; Antioxidants; Apoptosis; Cations, Divalent; Cell Survival; Copper; DNA Damage; HL-60 Cells; Humans; Hydrogen Peroxide; In Vitro Techniques; Leukocytes, Mononuclear; Mice; Mice, Inbred BALB C; Oxidants; Reactive Oxygen Species; Resveratrol; Stilbenes; T-Lymphocytes | 2009 |
Design, synthesis, biological and structural evaluation of functionalized resveratrol analogues as inhibitors of quinone reductase 2.
Topics: Anilides; Catalytic Domain; Crystallography, X-Ray; Drug Design; Enzyme Activation; Enzyme Inhibitors; Humans; Inhibitory Concentration 50; Molecular Structure; Quinone Reductases; Resveratrol; Small Molecule Libraries; Stilbenes | 2013 |
A facile and rapid access to resveratrol derivatives and their radioprotective activity.
Topics: Animals; Apoptosis; Boronic Acids; Catalysis; Gamma Rays; Oxidation-Reduction; Palladium; Radiation-Protective Agents; Rats; Resveratrol; Stilbenes; Structure-Activity Relationship; Styrenes; Thymocytes | 2016 |
Synthesis of resveratrol derivatives as new analgesic drugs through desensitization of the TRPA1 receptor.
Topics: Analgesics; Animals; Calcium Channels; Ganglia, Spinal; HEK293 Cells; Humans; Inhibitory Concentration 50; Nerve Tissue Proteins; Pain; Patch-Clamp Techniques; Rats; Resveratrol; Stilbenes; Transient Receptor Potential Channels; TRPA1 Cation Channel | 2017 |