dactinomycin has been researched along with kaempferol in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P | 1 |
Dairi, T; Hoang, NN; Ki, DW; Kodama, T; Lae, KZW; Lee, YE; Morita, H; Ngwe, H; Win, NN; Wong, CP | 1 |
Ciolino, HP; Daschner, PJ; Yeh, GC | 1 |
Cantabrana, B; Hidalgo, A; Revuelta, MP | 1 |
4 other study(ies) available for dactinomycin and kaempferol
Article | Year |
---|---|
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 |
Flavonoids from Woodfordia fruticosa as potential SmltD inhibitors in the alternative biosynthetic pathway of peptidoglycan.
Topics: DNA Ligase ATP; Dose-Response Relationship, Drug; Enzyme Inhibitors; Flavonoids; Molecular Structure; Peptidoglycan; Stenotrophomonas maltophilia; Structure-Activity Relationship; Woodfordia | 2021 |
Dietary flavonols quercetin and kaempferol are ligands of the aryl hydrocarbon receptor that affect CYP1A1 transcription differentially.
Topics: Binding, Competitive; Cell Nucleus; Cytochrome P-450 CYP1A1; Dactinomycin; DNA Probes; Dose-Response Relationship, Drug; Flavonoids; Flavonols; Gene Expression Regulation; Humans; Kaempferols; Ligands; Polychlorinated Dibenzodioxins; Promoter Regions, Genetic; Quercetin; Receptors, Aryl Hydrocarbon; Response Elements; RNA, Messenger; Time Factors; Transcription, Genetic; Transfection; Tumor Cells, Cultured | 1999 |
Mechanisms involved in kaempferol-induced relaxation in rat uterine smooth muscle.
Topics: Adenylyl Cyclase Inhibitors; Animals; Antimetabolites; Cyclic AMP; Cyclic AMP-Dependent Protein Kinases; Cycloheximide; Dactinomycin; Dideoxyadenosine; Drug Synergism; Eflornithine; Enzyme Inhibitors; Female; Flavonoids; In Vitro Techniques; Kaempferols; Muscle Relaxation; Muscle, Smooth; Papaverine; Phosphodiesterase Inhibitors; Potassium Chloride; Protein Synthesis Inhibitors; Quercetin; Rats; Rats, Wistar; Serine Proteinase Inhibitors; Spermine; Thionucleotides; Tosylphenylalanyl Chloromethyl Ketone; Uterine Contraction; Uterus | 2000 |