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OXA-11 (FAK-IN-16) is an orally active, selective focal adhesion kinase (FAK) inhibitor with antitumor activity. It inhibits FAK phosphorylation at tyrosine 397 in a dose-dependent manner and suppresses TOV21G tumor growth. It is used in cancer research.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
1 mg | $1,590 | In Stock | |
5 mg | $3,200 | In Stock | |
10 mg | $4,290 | In Stock |
Description | OXA-11 (FAK-IN-16) is an orally active, selective focal adhesion kinase (FAK) inhibitor with antitumor activity. It inhibits FAK phosphorylation at tyrosine 397 in a dose-dependent manner and suppresses TOV21G tumor growth. It is used in cancer research. |
Targets&IC50 | FAK:1.2 pM |
In vitro | OXA-11 is a selective photophosphorylation inhibitor of plaque adhesion kinase (FAK) with an IC50 of 1.2 pM. In 3-D culture, OXA-11 inhibited the proliferation of tumor cells, with EC50 of 9 nM in TOV21G cells and 0.3 nM in IGROV1 cells, and promoted apoptosis of tumor cells, with EC50 of 31 nM in TOV21G cells. The EC50 of IGROV1 cells was 0.5 nM. [1] |
In vivo | Intragastric administration of OXA-11 (40-120 mg/kg, soluble in 20% Trappsol) can reduce tumor vascular distribution and infiltration in mice, and when administered together with anti-VEGFR-2 antibody DC101, can reduce pancreatic neuroendocrine tumor metastasis in RIP-Tag2 mice. [1] |
Alias | OXA11, FAK-IN-16 |
Molecular Weight | 759.8 |
Formula | C37H49F3N7O5P |
Cas No. | 1257994-15-2 |
Smiles | N(C1=C2C(=C(C=C1)[C@H]3CC[C@@H](CC3)N4CCN(C)CC4)CN(C)C2=O)C=5C(C(F)(F)F)=CN=C(NC6=C(OC)C=C(CP(OCC)(OCC)=O)C=C6)N5 |
Relative Density. | 1.299 g/cm3 (Predicted) |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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