Information Ensartinib (X-396) dihydrochloride Ensartinib (X-396) is a potent new-generation ALK inhibitor with high activity against a broad range of known crizotinib-resistant ALK mutations and CNS metastases. It potently inhibits both wild-type ALK and ALK variants (F1174, C1156Y, L1196M, S1206R, T1151, and G1202R mutants) with in vitro IC50s of Targets TPM3-TRKA (Cell-free assay); TRKC (Cell-free assay); GOPC-ROS1 (Cell-free assay); ALK (Cell-free assay); ALK variants (Cell-free assay) In vitro Ensartinib potently inhibits both wild-type ALK and all evaluated ALK variants (F1174, C1156Y, L1196M, S1206R, T1151, and G1202R mutants) with in vitro IC50s of
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Ensartinib (X-396) dihydrochloride
CAS number:2137030-98-7 molecular formula:C26H29Cl4FN6O3
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| Chinese alias | - | ||
| English alias | Ensartinib hydrochloride | Ensartinib hydrochloride (USAN) | 3-Pyridazinecarboxamide, 6-amino-5-((1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)-N-(4-(((3R,5S)-3,5-dimethyl-1-piperazinyl)carbonyl)phenyl)-, hydrochloride (1:2) | UNII-C2FR6VT1BQ | Ensartinib di | ||
| CAS number | 2137030-98-7 | molecular formula | C26H29Cl4FN6O3 |
| molecular weight | 634.36 g/mol | Exact mass | ≥98% |
| PSA | 122.000 Ų | logp | 5.051 |
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