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T1791LCeritinib dihydrochlorideLDK378 dihydrochloride；双盐酸盐色瑞替尼
Ceritinib dihydrochloride is a selective, orally bioavailable and ATP-competitive inhibitor of ALK tyrosine kinase(IC50 of 200 pM), and also inhibits IGF-1R, InsR, and STK22D (IC50 values of 8, 7, and 23 nM, respectively), shows great antitumor potency
价 格：￥电议型 号：T1791L产 地：中国大陆
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T1791CeritinibLDK378；色瑞替尼
Ceritinib (LDK378) is a specific ALK inhibitor (IC50: 0.2 nM).
价 格：￥电议型 号：T1791产 地：中国大陆
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T1791LDK378LDK378,Ceritinib,
Ceritinib (LDK378) is a specific ALK inhibitor (IC50: 0.2 nM).
价 格：￥电议型 号：T1791产 地：美洲
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T1791LLDK378 dihydrochlorideLDK378 dihydrochloride,Ceritinib dihydrochloride,
Ceritinib dihydrochloride is a selective, orally bioavailable and ATP-competitive inhibitor of ALK tyrosine kinase(IC50 of 200 pM), and also inhibits IGF-1R, InsR, and STK22D (IC50 values of 8, 7, and 23 nM, respectively), shows great antitumor potency
价 格：￥电议型 号：T1791L产 地：美洲
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T30776c-Ceritinib TFA salt；化合物 T30776Coupleable ceritinib；Coupleable ceritinib
c-Ceritinib TFA salt is a coupleable ceritinib analog with a linker which also binds multiple other kinases, including FAK1, RSK1/2, ERK1/2, CAMKK2 and FER.
价 格：￥电议型 号：T30776产 地：中国大陆
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T1791LCeritinib dihydrochloride；双盐酸盐色瑞替尼LDK378 dihydrochloride；LDK378 dihydrochloride|||双盐酸盐色瑞替尼
Ceritinib dihydrochloride (LDK378 dihydrochloride) is a selective, orally bioavailable and ATP-competitive inhibitor of ALK tyrosine kinase(IC50 of 200 pM), and also inhibits IGF-1R, InsR, and STK22D (IC50 values of 8, 7, and 23 nM, respectively), shows great antitumor potency
价 格：￥电议型 号：T1791L产 地：中国大陆
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T1791Ceritinib；色瑞替尼LDK378；色瑞替尼|||LDK378
Ceritinib (LDK378) is a specific ALK inhibitor (IC50: 0.2 nM).
价 格：￥电议型 号：T1791产 地：中国大陆
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T10766Ceritinib D7；化合物 T10766LDK378 D7；LDK378 D7
Ceritinib D7 (LDK378 D7) is a deuterium-labeled Ceritinib. Ceritinib is an ATP-competitive inhibitor of ALK tyrosine kinase.
价 格：￥电议型 号：T10766产 地：中国大陆
