dihydrosanguinarine has been researched along with berberine in 2 studies
*Berberine: An alkaloid from Hydrastis canadensis L., Berberidaceae. It is also found in many other plants. It is relatively toxic parenterally, but has been used orally for various parasitic and fungal infections and as antidiarrheal. [MeSH]
*Berberine: An alkaloid from Hydrastis canadensis L., Berberidaceae. It is also found in many other plants. It is relatively toxic parenterally, but has been used orally for various parasitic and fungal infections and as antidiarrheal. [MeSH]
| Studies (dihydrosanguinarine) | Trials (dihydrosanguinarine) | Recent Studies (post-2010) (dihydrosanguinarine) | Studies (berberine) | Trials (berberine) | Recent Studies (post-2010) (berberine) |
|---|---|---|---|---|---|
| 28 | 0 | 17 | 4,106 | 102 | 2,791 |
| Protein | Taxonomy | dihydrosanguinarine (IC50) | berberine (IC50) |
|---|---|---|---|
| Acetylcholinesterase | Electrophorus electricus (electric eel) | 0.7827 | |
| Lysine-specific histone demethylase 1A | Homo sapiens (human) | 6.97 | |
| Cholinesterase | Homo sapiens (human) | 1.09 | |
| Acetylcholinesterase | Homo sapiens (human) | 0.4 | |
| Aldo-keto reductase family 1 member C3 | Homo sapiens (human) | 4.99 | |
| Aldo-keto reductase family 1 member C2 | Homo sapiens (human) | 6.71 | |
| Cholinesterase | Equus caballus (horse) | 9.4 | |
| Cytochrome P450 1B1 | Homo sapiens (human) | 0.9747 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheng, P; Kang, W; Liu, S; Liu, W; Qing, Z; Xie, H; Zeng, J; Zhou, J | 1 |
| Gao, L; Merz, KH; Schmitz, HJ; Schrenk, D | 1 |
2 other study(ies) available for dihydrosanguinarine and berberine
| Article | Year |
|---|---|
Synthesis of 5-methyl phenanthridium derivatives: a new class of human DOPA decarboxylase inhibitors.
Topics: Animals; Aromatic Amino Acid Decarboxylase Inhibitors; Enzyme Activation; Humans; Inhibitory Concentration 50; Molecular Structure; Phenanthridines; Rats | 2014 |
Characterization of the cytotoxicity of selected Chelidonium alkaloids in rat hepatocytes.
Topics: Alkaloids; Animals; Benzophenanthridines; Berberine; Cells, Cultured; Chelidonium; Chemical and Drug Induced Liver Injury; Dose-Response Relationship, Drug; Glutathione; Hepatocytes; Isoquinolines; Male; Molecular Structure; Primary Cell Culture; Rats, Wistar; Structure-Activity Relationship | 2019 |