Chemical Structure : CQ3196
Catalog No.: PC-25339Not For Human Use, Lab Use Only.
CQ3196 is a potent and orally bioavailable RIO kinase 2 (RIOK2) inhibitor with binding Kd of 14 nM, suppresses RIOK2 ATPase activity in vitro with IC50 of 72 nM in an ADP-Glo kinase assays.
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CQ3196 is a potent and orally bioavailable RIO kinase 2 (RIOK2) inhibitor with binding Kd of 14 nM, suppresses RIOK2 ATPase activity in vitro with IC50 of 72 nM in an ADP-Glo kinase assays.
CQ3196 displays potent inhibitory effects on the proliferation of gastric cancer cells, with IC50 values of 0.46 μM in HGC-27 and 0.73 μM in AGS, as well as chronic myelogenous leukemia cells (IC50 = 0.90 μM in K562).
CQ3196 induces cell apoptosis at indicated concentrations in HGC-27 and AGS cells, modulates ribosome function and protein synthesis.
CQ3196 significantly decreases the phosphorylation of AKT in HGC-27 cells from 300 nM.
CQ3196 (25 mg/kg or 50 mg/kg), oral) inhibits tumor growth in the HGC-27 Tumor xenografted model.
M.Wt | 577.61 | |
Formula | C30H30F3N7O2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Haowen Ma, et al. J Med Chem. 2025 Aug 14. doi: 10.1021/acs.jmedchem.5c01424.
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