- Cat. No.
- A11001
Y-27632 2HCl
Y-27632 is a Rho-Associated Coil Kinase (ROCK) inhibitor that increases the cloning efficiency of human embryonic stem cells (hESCs).
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Rho-associated protein kinase (ROCK) inhibitors act on ROCK1 and ROCK2, effectors of the small G protein Rho. Active Rho binds ROCK, which phosphorylates myosin light chain phosphatase and other substrates of the actin cytoskeleton. The resulting actomyosin contraction drives stress fiber formation, cell migration and smooth muscle tone. A 1997 study with Y-27632 linked ROCK to calcium sensitization of smooth muscle contraction in hypertensive rat models. In 2007 Y-27632 was shown to permit survival of dissociated human embryonic stem cells, and it remains common in stem cell culture. Fasudil HCl, ripasudil and thiazovivin are further ROCK inhibitors in this list.
Y-27632 is a Rho-Associated Coil Kinase (ROCK) inhibitor that increases the cloning efficiency of human embryonic stem cells (hESCs).
Y-27632 is an ATP-competitive inhibitor of ROCK-I and ROCK-II, with Ki of 220 nM and 300 nM for ROCK-I and ROCK-II, respectively.
Y-27632 hydrochloride hydrate is a selective inhibitor of Rho-associated protein kinases (ROCK-I and ROCK-II), exhibiting ATP-competitive activity with IC50 values of 220 nM and 300 nM, respectively. This compound has been shown to reduce Doxorubicin-induced apoptosis in human cardiac stem cells and suppress apoptosis in dissociation-induced murine prostate stem/progenitor cells. Additionally, Y-27632 hydrochloride hydrate enhances the differentiation of human induced pluripotent stem cells (hIPSCs) towards a mesendodermal lineage by modulating epithelial-mesenchymal transition.
Synonyms: AT-877; HA-1077; HA-1077 Hydrochloride
Fasudil HCl is a cyclic nucleotide-dependent protein kinase inhibitor and Rho-associated kinase inhibitor (IC50 = 10.7 μM).
Synonyms: ROCK-IN-2; TC-S 7001; BAY-549
Azaindole 1 (BAY-549) is a highly potent inhibitor of human ROCK-1 and ROCK-2 isoenzymes with IC50 values of 0.6 and 1.1 nM, respectively.
Synonyms: K 115
Ripasudil (K-115) is potent ROCK inhibitor with IC50 of 51 nM and 19 nM for ROCK1 and ROCK2, respectively, used for the treatment of glaucoma and ocular hypertension.
Synonyms: GSK269962A
GSK 269962 is a potent Rho kinase (ROCK) inhibitor (IC50 values are 1.6 and 4 nM for recombinant human ROCK1 and ROCK2 respectively).
GSK429286A is a cell-permeable, selective small molecule inhibitor of Rho-associated, coiled-coil containing protein kinase (ROCK).
RKI-1313 is a negative control for RKI-1447 which is a potent inhibitor of the Rho-associated ROCK kinases with anti-invasive and antitumor activities in breast cancer.
Thiazovivin is a selective inhibitor of Rho-associated kinase (ROCK).
Y-33075 is ROCK (Rho-associated coiled coil-forming protein kinase) inhibitor.
Y-33075 dihydrochloride is a selective ROCK inhibitor with an IC50 of 3.6 nM.
AT13148 is a novel oral multi-AGC kinase inhibitor with potent pharmacodynamic and antitumor activity, which shows a distinct mechanism of action from other AKT inhibitors.
SR 3677 is a potent and selective Rho-kinase inhibitor (IC50 values are 3 and 56 nM for ROCK-II and ROCK-I respectively).
Synonyms: RKI 1447. ROCK Inhibitor XIII
RKI-1447 is a potent inhibitor of the Rho-associated ROCK kinases with anti-invasive and antitumor activities in breast cancer.
Synonyms: Rho Kinase Inhibitor IV
Glycyl-H 1152 2HCl is a selective and potent ROCK inhibitor (IC50 values are 0.0118, 2.35, 2.57, 3.26, > 10 and >10 uM for ROCKII, Aurora A, CAMKII, PKG, PKA and PKC respectively.)
Synonyms: Fasudil dihydrochloride; HA1077
HA-1077 inhibits vascular smooth muscle contraction by acting as an intracellular Ca2+ antagonist.
Synonyms: ROCK-II inhibitor
Chroman 1 is a highly potent and selective ROCK II inhibitor.
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.
H-1152 dihydrochloride, 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.
Synonyms: HA-1100
Hydroxyfasudil, metabolite of Fasudil, is a potent Rho-kinase inhibitor and vasodilator.
Synonyms: HA-1100 hydrochloride
Hydroxyfasudil hydrochloride, metabolite of Fasudil, is a potent Rho-kinase inhibitor and vasodilator.
Synonyms: SLx 2119; ROCK inhibitor; KD-025
SLx-2119 is a small molecule and selective inhibitor of ROCK2 with IC50 of 105 nM; > 200 fold selecivity over ROCK1(IC50 =24 uM).
Synonyms: SAR 407899
SAR407899 is a potent and selective Rho kinase inhibitor with promising antihypertensive activity.