CFI-401870 

CFI-401870 is an orally active threonine tyrosine kinase (TKK (Mps1)) inhibitor with an IC₅₀ of 3.1 nM. CFI-401870 exhibits IC₅₀s against PLK4, KDR, AURKA and other kinases such as AURKB/INCENP were all greater than 1 μM.CFI-401870 inhibits the growth of various cancer cells, causing chromosome lag, an increase in aneuploidy and cell cycle arrest. CFI-401870 can be used for the study of cancers such as colon cancer^[1].

CFI-401870 inhibits MDA-MB-468, HCT-116 and OVCAR-3 cell proliferation with GI₅₀s of 36, 17 and 80 nM^[1].
CFI-401870 (0.05-3 μM, 48 h) induces G2/M phase arrest in a concentration-dependent manner, accompanied by a significant increase in the proportion of polyploid cells in HCT116 cells^[1].
CFI-401870 (0.1-0.5 μM, 6-28 h) leads to abnormal chromosome arrangement and defects in the spindle checkpoint in HCT116 cells^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

CFI-401870 (23-35 mg/kg, p.o., once daily for 21 days) demonstrates significant anti-tumor activity in multiple xenograft models of HCT116 colon cancer, MDA-MB-468 breast cancer and SW48 colon cancer in mice^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

493.60

C₃₀H₃₁N₅O₂

1430741-35-7

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Please store the product under the recommended conditions in the Certificate of Analysis.

• [1]. Liu Y, et al. The Discovery of Orally Bioavailable Tyrosine Threonine Kinase (TTK) Inhibitors: 3-(4-(heterocyclyl)phenyl)-1H-indazole-5-carboxamides as Anticancer Agents. J Med Chem. 2015 Apr 23;58(8):3366-92.  [Content Brief]