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Submit ReviewCeritinib is a highly potent anaplastic lymphoma kinase (ALK) inhibitor (IC50 = 0.2 nM). Also displays potent inhibition of insulin receptor (IR), insulin-like growth factor receptor 1 (IGF1R), serine/threonine-protein kinase STK22D and FLT3 (IC50 values are 7, 8, 23 and 60 nM, respectively). Inhibits tumor growth in Karpas299 and H2228 rat xenograft models.
分子量 | 558.14 |
公式 | C28H36ClN5O3S |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1032900-25-6 |
PubChem ID | 57379345 |
InChI Key | VERWOWGGCGHDQE-UHFFFAOYSA-N |
Smiles | CC(C)OC1=C(NC2=NC=C(Cl)C(NC3=C(C=CC=C3)[S](=O)(=O)C(C)C)=N2)C=C(C)C(=C1)C1CCNCC1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 2.79 | 5 温和加热 | |
ethanol | 2.79 | 5 温和加热 |
以下数据基于产品分子量 558.14。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.05 mM | 35.83 mL | 179.17 mL | 358.33 mL |
0.25 mM | 7.17 mL | 35.83 mL | 71.67 mL |
0.5 mM | 3.58 mL | 17.92 mL | 35.83 mL |
2.5 mM | 0.72 mL | 3.58 mL | 7.17 mL |
参考文献是支持产品生物活性的出版物。
Marsilje et al (2013) Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diam J.Med.Chem. 56 5675 PMID: 23742252
If you know of a relevant reference for Ceritinib, please let us know.
关键词: Ceritinib, Ceritinib supplier, LDK378, ALK, inhibitors, inhibits, highly, potent, Anaplastic, lymphoma, kinase, insulin, receptor, InsR, insulin-like, growth, factor, IGF1R, FLT3, STK22D, Insulin, and, Receptors, 6905, Tocris Bioscience
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