pinocembrin has been researched along with isosakuranetin in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (33.33) | 18.2507 |
2000's | 1 (16.67) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Baird, WM; Cassady, JM; Cook, VM; Ho, DK; Liu, YL | 1 |
Habtemariam, S | 1 |
Bergamo, DC; Bolzani, Vda S; Casanova, DC; Cavalheiro, AJ; Furlan, M; Guimarães, EF; Kato, MJ; Lago, JH; Morandim, Ade A; Ramos, CS; Young, MC | 1 |
Itoh, T; Sakakibara, H; Shimoi, K; Takemura, H; Yamamoto, K | 1 |
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P | 1 |
Erdoğan, Ş; Özbakır Işın, D | 1 |
6 other study(ies) available for pinocembrin and isosakuranetin
Article | Year |
---|---|
Isolation of potential cancer chemopreventive agents from Eriodictyon californicum.
Topics: Animals; Anticarcinogenic Agents; Benzo(a)pyrene; Cells, Cultured; Cricetinae; Depression, Chemical; DNA, Neoplasm; Female; Flavonoids; Plants, Medicinal; Pregnancy | 1992 |
Flavonoids as inhibitors or enhancers of the cytotoxicity of tumor necrosis factor-alpha in L-929 tumor cells.
Topics: Animals; Apoptosis; Drug Synergism; Flavonoids; Mice; Tumor Cells, Cultured; Tumor Necrosis Factor-alpha | 1997 |
Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum.
Topics: Antifungal Agents; Benzoates; Brazil; Chromatography, Thin Layer; Cladosporium; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Piper; Plant Leaves; Plants, Medicinal | 2004 |
Selective inhibition of methoxyflavonoids on human CYP1B1 activity.
Topics: Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 CYP1A1; Cytochrome P-450 CYP1A2; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP1B1; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System; Flavonoids; Humans; Models, Molecular; Structure-Activity Relationship | 2010 |
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship | 2012 |
A DFT study on OH radical scavenging activities of eriodictyol, Isosakuranetin and pinocembrin.
Topics: Antioxidants; Flavonoids; Free Radical Scavengers; Humans; Hydrogen; Protons; Thermodynamics | 2022 |