sanguinarine has been researched along with chelerythrine chloride in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lasovský, J; Lenfeld, J; Preininger, V; Simánek, V; Walterová, D | 1 |
Bernardo, PH; Chai, CL; Hung, AW; Mok, HY; Moore, FK; Sivaraman, T; Wan, KF; Xu, J; Yu, VC | 1 |
Artini, M; Barbato, G; Bombardelli, E; Cellini, A; Morazzoni, P; Papa, R; Scoarughi, GL; Selan, L | 1 |
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P | 1 |
4 other study(ies) available for sanguinarine and chelerythrine chloride
Article | Year |
---|---|
Inhibition of liver alanine aminotransferase activity by some benzophenanthridine alkaloids.
Topics: Alanine Transaminase; Alkaloids; Animals; Benzophenanthridines; In Vitro Techniques; Isoquinolines; Kinetics; Liver; Male; Phenanthridines; Rats; Rats, Inbred Strains; Time Factors | 1981 |
Structure-activity relationship studies of phenanthridine-based Bcl-XL inhibitors.
Topics: bcl-X Protein; Computer Simulation; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Structure; Mutation; Phenanthridines; Structure-Activity Relationship | 2008 |
Bacterial biofilm formation inhibitory activity revealed for plant derived natural compounds.
Topics: Aesculus; Anti-Bacterial Agents; Biofilms; Biological Products; Chelidonium; Krameriaceae; Membrane Proteins; Microbial Sensitivity Tests; Plant Extracts; Plants; Staphylococcus aureus; Staphylococcus epidermidis | 2012 |
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 |