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Sitravatinib (MGCD516) is an orally active receptor tyrosine kinase (RTK) inhibitor. Inhibition of Axl, MER, VEGFR3, VEGFR2, VEGFR1, KIT, FLT3, DDR2, DDR1, TRKA, and TRKB at 1.5 nM, 2 nM, 2 nM, 5 nM, 6 nM, 6 nM, 8 nM, 0.5 nM, respectively. 29 nM, 5 nM and 9 nM. Sitravatinib alone has a potent antitumor effect and enhances pD-1 blockade activity by promoting the antitumor immune microenvironment.
Mol Cell Proteomics. 2024 Mar 28;23(5):100756.
Dynamic proteomic changes in tumor and immune organs reveal systemic immune response to tumor development
Sitravatinib purchased from AbMole
| Molecular Weight | 629.68 |
| Formula | C33H29F2N5O4S |
| CAS Number | 1123837-84-2 |
| Solubility (25°C) | DMSO ≥ 26 mg/mL |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
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| Regorafenib
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| Nintedanib
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Products are for research use only. Not for human use. We do not sell to patients.
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