About 8 results found for searched term "ROCK-IN-4" (0.134 seconds)
Cat.No. | Name | Target |
---|---|---|
M49542 | ROCK-IN-4 | ROCK |
ROCK-IN-4 is a potent ROCK inhibitor maintaining NO releasing ability. | ||
M5168 | GSK269962A | ROCK |
GSK 269962 | ||
GSK269962A is a potent ROCK inhibitor with IC50 values of 1.6 and 4 nM for recombinant human ROCK1 and ROCK2, respectively. | ||
M9678 | SAR407899 | ROCK |
SAR407899 is a potent and selective, ATP-competitive ROCK inhibitor with IC50 of 135 nM for ROCK-2, and Kis of 36 nM and 41 nM for human and rat ROCK-2, respectively. | ||
M13730 | RKI-1447 dihydrochloride | ROCK |
RKI 1447 dihydrochloride is a potent and selective ROCK inhibitor with IC50s of 14.5 and 6.2 nM for ROCK1 and ROCK2, respectively. RKI 1447 dihydrochloride suppresses colorectal carcinoma cell growth and promotes apoptosis. | ||
M13732 | SAR407899 hydrochloride | ROCK |
SAR407899 hydrochloride is a selective, potent and ATP-competitive ROCK inhibitor, with an IC50 of 135 nM for ROCK-2, and Kis of 36 nM and 41 nM for human and rat ROCK-2, respectively. | ||
M20999 | Y-27632 | ROCK |
Y-27632 is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM in a cell-free assay, exhibits >200-fold selectivity over other kinases, including PKC, cAMP-dependent protein kinase, MLCK and PAK. | ||
M49533 | GSK269962A hydrochloride | ROCK |
GSK269962A hydrochloride (GSK 269962 hydrochloride) is a potent ROCK inhibitor with IC50s of 1.6 and 4 nM for recombinant human ROCK1 and ROCK2 respectively. | ||
M49772 | Akt/ROCK-IN-1 | ROCK |
Akt/ROCK-IN-1 (B12) is a dual inhibitor for Akt and ROCK, with the IC50s of 0.023 nM and 1.47 nM, respectively. |
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