research use only
Cat.No.S7654
| Related Targets | EGFR VEGFR JAK PDGFR FGFR Src HIF FLT FLT3 HER2 |
|---|---|
| Other FAK Inhibitors | PF-562271 (VS-6062) PF-573228 VS-4718 (PND-1186) PF-562271 HCl PF-562271 Besylate TAE226 (NVP-TAE226) GSK2256098 PF-431396 Y15 Ifebemtinib (IN10018, BI-853520) |
| Cell Lines | Assay Type | Concentration | Incubation Time | Formulation | Activity Description | PMID |
|---|---|---|---|---|---|---|
| HepG2 | Function assay | reduced and retarded multicellular spheroid formation | 29332411 | |||
| Bel-7402 | Function assay | reduced and retarded multicellular spheroid formation | 29332411 | |||
| PC3-mm2 | Function assay | Treatment of PC3-mm2 cells with defactinib led to a time- and dose-dependent inhibition of FAK phosphorylation | 26530902 | |||
| BON | Cell viability assay | 72 h | GI50=5.42 μM | 25971297 | ||
| GGP-1 | Cell viability assay | 72 h | GI50=4.90 μM | 25971297 | ||
| CM | Cell viability assay | 72 h | GI50=1.77 μM | 25971297 | ||
| KB-3-1 | qHTS assay | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 31515284 | |||
| Click to View More Cell Line Experimental Data | ||||||
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In vitro |
DMSO
: 100 mg/mL
(195.89 mM)
Water : Insoluble Ethanol : Insoluble |
|
In vivo |
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| Molecular Weight | 510.49 | Formula | C20H21F3N8O3S |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 1073154-85-4 | Download SDF | Storage of Stock Solutions |
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| Synonyms | PF-04554878 | Smiles | CNC(=O)C1=CC=C(C=C1)NC2=NC=C(C(=N2)NCC3=NC=CN=C3N(C)S(=O)(=O)C)C(F)(F)F | ||
| Targets/IC50/Ki |
FAK
|
|---|---|
| In vitro |
In taxane-sensitive (SKOV3ip1) and taxane-resistant (SKOV3-TR) cell lines, Defactinib (VS-6063) significantly inhibits pFAK (Tyr397) expression. The combination of this compound synergistically decreases proliferation and increases apoptosis in SKOV3ip1, SKOV3-TR, HeyA8 and HeyA8-MDR cells. Its combination with Y15 also synergistically decreases viability, clonogenicity, and cell attachment in thyroid cancer cell lines. |
| In vivo |
In both PTX-sensitive and PTX-resistant models, Defactinib (VS-6063) (50 mg/kg p.o.) enhances tumor growth inhibition. |
References |
|
| Methods | Biomarkers | Images | PMID |
|---|---|---|---|
| Western blot | HER2 pY1248 / FAK pY397 / AKT pS473 / p-ERK pIGF1R / IGF1R / E-cadherin / vimentin / ZEB-1 |
|
27638858 |
| Immunofluorescence | pFAK (Tyr 397) / pYB-1 (Ser 102) |
|
24062525 |
| Growth inhibition assay | Cell viability |
|
25971297 |
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