fasudil has been researched along with HIV Coinfection in 2 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Fasudil is a potent inhibitor for various protein kinases such as myosin light chain kinase and protein kinase C." | 1.30 | Suppression of HIV-1 replication in peripheral blood mononuclear cells by fasudil. ( Adachi, A; Akari, H; Hiwada, H; Koyama, AH; Saito, Y; Takayanagi, N; Yamamoto, Y, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sato, T | 1 |
| Asamitsu, K | 1 |
| Yang, JP | 1 |
| Takahashi, N | 1 |
| Tetsuka, T | 1 |
| Yoneyama, A | 1 |
| Kanagawa, A | 1 |
| Okamoto, T | 1 |
| Akari, H | 1 |
| Yamamoto, Y | 1 |
| Hiwada, H | 1 |
| Saito, Y | 1 |
| Takayanagi, N | 1 |
| Koyama, AH | 1 |
| Adachi, A | 1 |
2 other studies available for fasudil and HIV Coinfection
| Article | Year |
|---|---|
Inhibition of human immunodeficiency virus type 1 replication by a bioavailable serine/threonine kinase inhibitor, fasudil hydrochloride.
Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Anti-HIV Agents; Base Sequence; Cell Line; DNA, Recom | 1998 |
Suppression of HIV-1 replication in peripheral blood mononuclear cells by fasudil.
Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Enzyme Inhibitors; HeLa Cells; HIV Infections; HIV-1; | 1998 |