fasudil has been researched along with Carbon Tetrachloride Poisoning in 1 studies
fasudil: intracellular calcium antagonist; structure in first source
fasudil : An isoquinoline substituted by a (1,4-diazepan-1-yl)sulfonyl group at position 5. It is a Rho-kinase inhibitor and its hydrochloride hydrate form is approved for the treatment of cerebral vasospasm and cerebral ischemia.
Carbon Tetrachloride Poisoning: Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ikeda, H | 1 |
| Kume, Y | 1 |
| Tejima, K | 1 |
| Tomiya, T | 1 |
| Nishikawa, T | 1 |
| Watanabe, N | 1 |
| Ohtomo, N | 1 |
| Arai, M | 1 |
| Arai, C | 1 |
| Omata, M | 1 |
| Fujiwara, K | 1 |
| Yatomi, Y | 1 |
1 other study available for fasudil and Carbon Tetrachloride Poisoning
| Article | Year |
|---|---|
Rho-kinase inhibitor prevents hepatocyte damage in acute liver injury induced by carbon tetrachloride in rats.
Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Androstadienes; Animals; Apoptosis; Carbon Tetrachlor | 2007 |