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Submit ReviewAZ 14145845 is a potent, and highly selective dual Mer/Axl kinase inhibitor (pIC50 = 7 nM and 7.8 nM in pAxl and pMer, respectively). In vivo, AZ 14145845 shows dose-dependent reduction of tumor growth in the Mer and Axl kinase Ba/F3 tumor xenograft model. AZ 14145845 combined with anti-PD1 antibodies and ionizing radiation increases survival in mice with tumors derived from MC38 cells in vivo. AZ 14145845 is orally bioavailable.
分子量 | 561.69 |
公式 | C32H35N9O |
储存 | Store at -20°C |
纯度 | ≥97% (HPLC) |
CAS Number | 2830555-70-7 |
PubChem ID | 156596359 |
InChI Key | CZIXXCVLEHVEBZ-UHFFFAOYSA-N |
Smiles | CC1=C(N=CC(C2=C(C)N(C)N=C2C)=C1)C3=NN=C(N(CC4=CN5C(C6=CC=C(CN(C)C)C=C6)=CN=C5C=C4)C)O3 |
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 | 56.17 | 100 | |
ethanol | 56.17 | 100 |
以下数据基于产品分子量 561.69。 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 |
---|---|---|---|
1 mM | 1.78 mL | 8.9 mL | 17.8 mL |
5 mM | 0.36 mL | 1.78 mL | 3.56 mL |
10 mM | 0.18 mL | 0.89 mL | 1.78 mL |
50 mM | 0.04 mL | 0.18 mL | 0.36 mL |
参考文献是支持产品生物活性的出版物。
McCoull et al (2021) Optimization of an Imidazo[1,2.a]pyridine series to afford highly selective type I1/2 Dual Mer/Axl kinase inhibitors with in vivo efficacy. J.Med.Chem. 64 13524 PMID: 34478292
If you know of a relevant reference for AZ 14145845, please let us know.
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