Axitinib, also known as AG013736, is an orally bioavailable tyrosine kinase inhibitor. Axitinib inhibits the proangiogenic cytokines vascular endothelial growth factor (VEGF) and platelet-derived growth factor receptor (PDGF), thereby exerting an anti-angiogenic effect. A xitinib has received FDA (27 January 2012), EMA (13 September 2012), MHRA (3 September 2012) and TGA (26 July 2012) approval for use as a treatment for renal cell carcinoma.
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Name | Axitinib |
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Molecular Formula | C22H18N4OS |
Molecular Weight | 386.47 |
Smile | CNC(=O)c1ccccc1Sc2ccc3c(c2)[nH]nc3/C=C/c4ccccn4 |
InChiKey | RITAVMQDGBJQJZ-FMIVXFBMSA-N |
InChi | InChI=1S/C22H18N4OS/c1-23-22(27)18-7-2-3-8-21(18)28-16-10-11-17-19(25-26-20(17)14-16)12-9-15-6-4-5-13-24-15/h2-14H,1H3,(H,23,27)(H,25,26)/b12-9+ |
CAS Number | 319460-85-0 |
MDL | MFCD09837898 |
Related CAS |
Packaging | Price | Availability | Purity | Shipping Time |
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Purity | 98% |
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Solubility | Soluble to 25 mM in DMSO |
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HS Code |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study |