oxidopamine hydrochloride has been researched along with gossypol acetic acid in 1 studies
| Studies (oxidopamine hydrochloride) | Trials (oxidopamine hydrochloride) | Recent Studies (post-2010) (oxidopamine hydrochloride) | Studies (gossypol acetic acid) | Trials (gossypol acetic acid) | Recent Studies (post-2010) (gossypol acetic acid) |
|---|---|---|---|---|---|
| 18 | 0 | 13 | 209 | 16 | 77 |
| Protein | Taxonomy | oxidopamine hydrochloride (IC50) | gossypol acetic acid (IC50) |
|---|---|---|---|
| Mcl-1 | Homo sapiens (human) | 1.2628 | |
| Valosin-containing protein | Homo sapiens (human) | 5.386 | |
| Muscarinic acetylcholine receptor M1 | Rattus norvegicus (Norway rat) | 1.17 | |
| Muscarinic acetylcholine receptor M3 | Rattus norvegicus (Norway rat) | 1.17 | |
| Muscarinic acetylcholine receptor M4 | Rattus norvegicus (Norway rat) | 1.17 | |
| Muscarinic acetylcholine receptor M5 | Rattus norvegicus (Norway rat) | 1.17 | |
| 60 kDa heat shock protein, mitochondrial | Homo sapiens (human) | 1.2 | |
| Muscarinic acetylcholine receptor M2 | Rattus norvegicus (Norway rat) | 1.17 | |
| 10 kDa heat shock protein, mitochondrial | Homo sapiens (human) | 1.2 | |
| 60 kDa chaperonin | Escherichia coli | 0.545 | |
| 10 kDa chaperonin | Escherichia coli | 0.545 |
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdeen, S; Chapman, E; Chitre, S; Hoang, QQ; Johnson, SM; Park, Y; Ray, AM; Salim, N; Sivinski, J; Stevens, M; Washburn, A | 1 |
1 other study(ies) available for oxidopamine hydrochloride and gossypol acetic acid
| Article | Year |
|---|---|
HSP60/10 chaperonin systems are inhibited by a variety of approved drugs, natural products, and known bioactive molecules.
Topics: Biological Products; Chaperonin 10; Chaperonin 60; Escherichia coli; Humans; Inhibitory Concentration 50; Protein Folding; Rafoxanide; Salicylanilides; Suramin | 2019 |