Name | belizatinib |
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Synonyms |
4-Fluoro-N-(6-{[4-(2-hydroxy-2-propanyl)-1-piperidinyl]methyl}-1-[cis-4-(isopropylcarbamoyl)cyclohexyl]-1H-benzimidazol-2-yl)benzamide
belizatinib Benzamide, 4-fluoro-N-[6-[[4-(1-hydroxy-1-methylethyl)-1-piperidinyl]methyl]-1-[cis-4-[[(1-methylethyl)amino]carbonyl]cyclohexyl]-1H-benzimidazol-2-yl]- TSR-011 |
Description | Belizatinib is an oral, dual, potent inhibitor of ALK and TRKA, TRKB, and TRKC, with IC50 of 0.7 nM for wild-type recombinant ALK kinase. |
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Related Catalog | |
Target |
IC50: 0.7 nM (ALK)[1] |
In Vitro | TSR-011 has antitumour activity in the clinical trials. |
In Vivo | TSR-011 exerts sustained potent inhibition of ALK-dependent tumour growth in mouse models[1]. |
References |
Density | 1.3±0.1 g/cm3 |
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Molecular Formula | C33H44FN5O3 |
Molecular Weight | 577.733 |
Exact Mass | 577.342834 |
LogP | 3.99 |
Index of Refraction | 1.631 |
Storage condition | -20℃ |
Hazard Codes | N |
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