Chemical Structure : CINS-1
Catalog No.: PC-28707Not For Human Use, Lab Use Only.
CINS-1 is a potent, specific RIO Kinase 1 (RIOK1) inhibitor with high binding affinity (ITC Kd=97 nM, AfRIOK1), binds to human RIOK1 with a Kd of 176 nM, exhibits antiproliferative activity against CRC cell lines HCT116 with IC50 of 7.81 uM.
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CINS-1 is a potent, specific RIO Kinase 1 (RIOK1) inhibitor with high binding affinity (ITC Kd=97 nM, AfRIOK1), binds to human RIOK1 with a Kd of 176 nM, exhibits antiproliferative activity against CRC cell lines HCT116 with IC50 of 7.81 uM.
CINS-1 exhibits poor inhibitory activity against VEGFR, EGFR, HER2, c-ABL, and AXL.
CINS-1 (10 uM) affects processing of 18S-E to 18S rRNA in CRC cells detected by FISH assay
CINS-1 activates P53-mediated nucleolar stress response in HCT116 cells.
CINS-1 (80 mg/kg, oral) significantly inhibited tumor growth subcutaneous xenograft model using human HCT116 cells.
| M.Wt | 354.41 | |
| Formula | C23H18N2O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Jiang Y, et al. Acta Pharm Sin B. 2026 Oct;16(10):6831-6851.

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