RKI-1447
RKI-1447 is a potent inhibitor of ROCK1 and ROCK2, with IC50 of 14.5 nM and 6.2 nM, respectively, has anti-invasive and antitumor activities. (In Vitro) :RKI-1447 is a Type I kinase inhibitor that binds the ATP binding site through interactions with the hinge region and the DFG motif. RKI-1447 suppresses phosphorylation of the ROCK substrates mLC-2 and MYPT-1 in human cancer cells, but has no effect on the phosphorylation levels of the AKT, MEK and S6 kinase at concentrations as high as 10 μM. RKI-1447 is also highly selective at inhibiting ROCK-mediated cytoskeleton re-organization. RKI-1447 inhibits migration, invasion and anchorage-independent tumor growth of breast cancer cells. (In Vivo) :RKI-1447 is highly effective at inhibiting the outgrowth of mammary tumors in a transgenic mouse model. RKI-1447 inhibits mammary tumor growth by 87% and on average the mammary tumors from RKI-1447 treated mice are 7.7 fold smaller compared to those tumors from mice treated with the vehicle control.
Product Specifications
CAS Number
1342278-01-6
Product Name Alternative
RKI-1447 | RKI1447 | RKI 1447. ROCK Inhibitor XIII
Purity
>98% (HPLC)
Solubility
DMSO: 65 mg/mL (199.16 mM)
Smiles
O=C (NC1=NC (C2=CC=NC=C2) =CS1) NCC3=CC=CC (O) =C3
Molecular Formula
C16H14N4O2S
Molecular Weight
326.37
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
1- (3-Hydroxybenzyl) -3- (4- (pyridin-4-yl) thiazol-2-yl) urea
Available Sizes
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