CFI402257
Modify Date: 2024-01-13 18:18:04
CFI402257 structure
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Common Name | CFI402257 | ||
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| CAS Number | 1610759-22-2 | Molecular Weight | 498.58 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C28H30N6O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of CFI402257CFI-402257 is a highly selective and orally bioavailable TTK and Mps1 inhibitor with Kis of 0.1 and 0.09 nM, respectively. |
| Name | CFI-402257 |
|---|---|
| Synonym | More Synonyms |
| Description | CFI-402257 is a highly selective and orally bioavailable TTK and Mps1 inhibitor with Kis of 0.1 and 0.09 nM, respectively. |
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| Related Catalog | |
| Target |
Mps1:1.7 nM (IC50, TTK) CYP2C9:13 μM (IC50) CYP2C19:8 μM (IC50) |
| In Vitro | CFI-402257 is highly selective to TTK. CFI-402257 is tested against a panel of human kinases at 1 μM and inhibits none of the 262 kinases tested. CFI-402257 is a potent inhibitor of cell growth[1]. CFI-402257 shows strong antineoplastic activity on a broad panel of human cancer-derived cell lines, and causes effects consistent with depletion or inhibition of Mps1. CFI-402257 inhibits Mps1 with an IC50 value of 1.2 nM, and is ATP competitive with a Ki value of 0.09 nM. CFI-402257 inhibits autophosphorylation of Mps1 at threonine 12/serine 15 with an EC50 value of 6.5 nM in cells exogenously expressing human Mps1. CFI-402257 exerts potent growth inhibitory activity across the vast majority of cell lines with a median IC50 value of 15 nM[2]. |
| In Vivo | The upper dose level for once-daily administration of CFI-402257 is between 6 and 6.5 mg/kg. CFI-402257 given orally QD shows dose-dependent activity in mice with established tumors from xenografted MDA-MB-231 human TNBC cells [5 mg/kg CFI-402257, tumor growth inhibition (TGI)=74%; 6 mg/kg, TGI=89%], from xenografted MDA-MB-468 human TNBC cells in mice (5 mg/kg, TGI=75%; 6 mg/kg, TGI=94%). CFI-402257 also demonstrates antitumor activity in a platinum-resistant PDX model of high-grade serous ovarian cancer (6.5 mg/kg, TGI=61%). CFI-402257 is found to be similarly efficacious in a platinum-sensitive PDX model of high-grade serous ovarian cancer[2]. |
| Cell Assay | Cells are treated with 20 pM to 10 μM CFI-402257 for 5 days. After 5 d, cell growth in each well is assessed by an SRB assay. SRB absorbance values are adjusted by subtracting the average of the baseline readings from untreated cells assessed 1 d after cell seeding. Relative cell growth is calculated by comparing vs. DMSO-treated cells. The concentrations at which cell growth is inhibited by 50% are calculated by using GraphPad Prism software[2]. |
| Animal Admin | Mice: CFI-402257 and the vehicle are administered by oral gavage, and carboplatin, anti–PD-1 antibody, and isotype control are administered by i.p. injection to mice as described earlier. Animal weights are monitored daily, and tumor volume is measured three times per week[2]. |
| References |
| Molecular Formula | C28H30N6O3 |
|---|---|
| Molecular Weight | 498.58 |
| CFI402257 |