ZT-12-037-01
ZT-12-037-01 is a potent, selective, ATP-competitive STK19 inhibitor with IC50 of 20.04 nM measured as percentage of NRAS phosphorylation; shows similar IC50 of 23.96 and 27.94 nM for STK19WTWT STK19D89N respectively; displays extremely high kinase selectivity using KINOMEscan against a panel of 468 diverse kinases using an in vitro ATP-site competition binding assay at 1 uM; efficiently inhibits phosphorylation of NRAS in a dose- and time-dependent manner, inhibits NRAS activity in a dose-dependent manner but does not affect the levels of H3K9 methylation; effectively inhibits NRAS signaling, including the MEK-ERK and PI3K pathways in SK-MEL-2 and WM2032 cells (with NRASQ61R), but the inhibition was much less effective in A375 or UACC62 cells (with NRASWT), effectively inhibits cell growth and induces apoptosis of SK-MEL-2 and WM2032 melanoma cells.
Product Specifications
CAS Number
2328073-61-4
Purity
>98% (HPLC)
Solubility
In Vitro: 1M HCl : 100 mg/mL (259.40 mM)
Smiles
COC1=CC2=NC (NC3CC3) =NC (NC4CCN (C (C) C) CC4) =C2C=C1OC
Molecular Formula
C21H31N5O2
Molecular Weight
385.512
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
N2-cyclopropyl-N4- (1-isopropylpiperidin-4-yl) -6,7-dimethoxyquinazoline-2,4-diamine
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