About 5 results found for searched term "H-1152" (0.124 seconds)
Cat.No. | Name | Target |
---|---|---|
M4938 | H-1152 | ROCK |
H-1152, an isoquinolinesulfonamide derivative, is a more specific, stronger and membrane-permeable inhibitor of Rho-kinase with a Ki value of 1.6 nM, but poor inhibitor of other serine/threonine kinases. | ||
M13727 | H-1152 dihydrochloride | ROCK |
H-1152 dihydrochloride is a membrane-permeable and selective ROCK inhibitor, with a Ki value of 1.6 nM, and an IC50 value of 12 nM for ROCK2. | ||
M49531 | Glycyl H-1152 hydrochloride | ROCK |
Glycyl H-1152 hydrochloride is a glycyl derivative of Rho-kinase inhibitors H-1152 dihydrochloride. | ||
M21177 | (-)-Enitociclib | CDK |
(-)-BAY-1251152; (-)-VIP152 | ||
(-)-Enitociclib ((-)-BAY-1251152) is an enantiomer of BAY-1251152 with a (-) spin. BAY-1251152 is a potent and highly selective inhibitor of cell cycle-dependent protein kinase (PTEF/CDK9). | ||
M21755 | Barasertib | Aurora Kinase |
AZD1152 | ||
Barasertib (AZD1152), a precursor of Barasertib-hQPA, is a highly selective Aurora B inhibitor with an IC50 of 0.37 nM in a cell-free assay. Barasertib (AZD1152) induces growth arrest and apoptosis in cancer cells. |
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