Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) with potential antineoplastic activity. Upon oral administration, ensartinib binds to and inhibits ALK kinase, ALK fusion proteins and ALK point mutation variants. Inhibition of ALK leads to the disruption of ALK-mediated signaling and eventually inhibits tumor cell growth in ALK-expressing tumor cells. ALK belongs to the insulin receptor superfamily and plays an important role in nervous system development. ALK is not expressed in healthy adult human tissue but ALK dysregulation and gene rearrangements are associated with a series of tumors; ALK mutations are associated with acquired resistance to small molecule tyrosine kinase inhibitors.
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Name | Ensartinib hydrochloride |
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Iupac Chemical Name | 6-aMino-5-((r)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)-n-(4-((3r,5s)-3,5-dimethylpiperazine-1-carbonyl)phenyl)pyridazine-3-carboxamide dihydrochloride |
Synonyms | Ensartinib hydrochloride;X-396 hydrochloride |
Molecular Formula | C26H29Cl4FN6O3 |
Molecular Weight | 634.36 |
Smile | Cl.Cl.NC1=C(C=C(N=N1)C(=O)NC1=CC=C(C=C1)C(=O)N1C[C@H](N[C@H](C1)C)C)O[C@H](C)C1=C(C(=CC=C1Cl)F)Cl |
InChiKey | IERUINQRGJAECT-ISUJJMBGSA-N |
InChi | InChI=1S/C26H27Cl2FN6O3.2ClH/c1-13-11-35(12-14(2)31-13)26(37)16-4-6-17(7-5-16)32-25(36)20-10-21(24(30)34-33-20)38-15(3)22-18(27)8-9-19(29)23(22)28;;/h4-10,13-15,31H,11-12H2,1-3H3,(H2,30,34)(H,32,36);2*1H/t13-,14+,15-;;/m1../s1 |
CAS Number | 2137030-98-7 |
Related CAS |
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Formulation | Off-white solid to white solid |
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Purity | 98% Min. |
Storage | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
Solubility | Soluble in DMSO, not in water |
Handling | |
Shipping Condition | Shipped under ambient temperature |
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[1]. Lovly CM, et al. Insights into ALK-driven cancers revealed through development of novel ALK tyrosine kinaseinhibitors. Cancer Res. 2011 Jul 15;71(14):4920-31.