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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名称 | 恩替替尼二盐酸盐 |
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Iupac 化学名称 | 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 |
同义词 | Ensartinib hydrochloride;X-396 hydrochloride; 恩替替尼 |
英文同义词 | Ensartinib hydrochloride;X-396 hydrochloride |
分子式 | C26H29Cl4FN6O3 |
分子量 | 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号 | 2137030-98-7 |
相关CAS号 |
包装 | 价格 | 库存 | 纯度 | 备货期 |
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大货 | 询价 | 询价 | 询价 |
外观性状 | 类白色至白色固体 |
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纯度 | 98% Min. |
存储 | 短期可在0-4度保存,数天至数月;长期可在-20度保存三年。 |
可溶性 | 可溶于DMSO;不溶于水 |
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运输条件 | 可在常温下运输 |
海关编码 |
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Mechanism | |
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Clinical study |
[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.