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 About 8 results found for searched term "ROCK-IN-32" (0.127 seconds)

Cat.No.  Name Target
M49541 ROCK-IN-32 ROCK
ROCK-IN-32 is a ROCK inhibitor, with an IC50 value of 11 nM for ROCK2.
M1817 Y-27632 dihydrochloride ROCK
Y27632; Y-27632 2HCl
Y-27632 is a potent, selective inhibitor of Rho-associated protein kinases (ROCK) with IC50 values of 140-220 nM for ROCK1 and ROCK2. In addition, Y-27632 inhibited LPA-induced entosis.
M5123 Y-39983 dihydrochloride ROCK
Y-33075 dihydrochloride
Y-39983 (Y-33075) dihydrochloride is a selective ROCK inhibitor with an IC50 of 3.6 nM, derived from Y-27632, inhibited ROCK more potently than Y-27632.
M13733 Y-33075 ROCK
Y 39983
Y-33075 is a selective ROCK inhibitor derived from Y-27632, and is more potent than Y-27632, with an IC50 of 3.6 nM.
M28439 CRT0066854  PKC
CRT0066854 is a potent and selective atypical PKC isoenzymes inhibitor. CRT0066854 is against full-length (FL) PKCι, PKCζ, and ROCK-II kinases with IC50 values of 132 nM, 639 nM, and 620 nM, respectively.
M29437 CRT0066854 hydrochloride  PKC
CRT0066854 hydrochloride is a potent and selective atypical PKCs inhibitor. CRT0066854 is against full-length (FL) PKCι, PKCζ, and ROCK-II kinases with IC50 values of 132 nM, 639 nM, and 620 nM, respectively.
M49536 Rho-Kinase-IN-1 ROCK
Rho-Kinase-IN-1 is a Rho kinase (ROCK) inhibitor (Ki values of 30.5 and 3.9 nM for ROCK1 and ROCK2, respectively) extracted from US20090325960A1, compound 1.008.
M56027 Y-33075 hydrochloride ROCK
Y-33075 hydrochloride (Y-39983) is a selective ROCK inhibitor derived from Y-27632, and is more potent than Y-27632, with an IC50 of 3.6 nM.



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