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| ARRY-424704, ARRY-704 Basic information |
Product Name: | ARRY-424704, ARRY-704 | Synonyms: | ARRY-424704, ARRY-704;AZD8330;2-(2-Fluoro-4-iodophenylamino)-N-(2-hydroxyethoxy)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxamide;ARRY424704;ARRY-424704;ARRY704;ARRY-704;AZD8330/ARRY-424704/arry-704/AZD8330/AZD-8330 | CAS: | 869357-68-6 | MF: | C16H17FIN3O4 | MW: | 461.23 | EINECS: | 642-441-7 | Product Categories: | Inhibitors;MAPK | Mol File: | 869357-68-6.mol | |
| ARRY-424704, ARRY-704 Chemical Properties |
density | 1.732 | storage temp. | Store at -20°C | solubility | ≥23.05 mg/mL in DMSO; insoluble in H2O; ≥46.1 mg/mL in EtOH | form | solid | pka | 14.31±0.10(Predicted) |
| ARRY-424704, ARRY-704 Usage And Synthesis |
Description | AZD 8330 is a selective allosteric inhibitor of MEK1/2 (IC50 = 7 nM). It blocks phosphorylation of ERK1/2 and inhibits proliferation of certain cancer cells. AZD 8330 is orally bioavailable, inhibits ERK phosphorylation in vivo, and reduces tumor growth in a Calu-6 nude rat xenograft model. | Uses | AZD8330 is an orally active and selective MEK inhibitor. | Definition | ChEBI: 2-(2-fluoro-4-iodoanilino)-N-(2-hydroxyethoxy)-1,5-dimethyl-6-oxo-3-pyridinecarboxamide is a pyridinecarboxamide. It is functionally related to a nicotinamide. | target | ERK phosphorylation | references | 1. feng k, wang c, zhou h, yang j, dong l, zhou k, et al. [effect of erk1/2 inhibitor azd8330 on human burkitt's lymphoma cell line raji cells and its mechanism]. zhonghua xue ye xue za zhi 2015,36:148-152.2. cohen rb, aamdal s, nyakas m, cavallin m, green d, learoyd m, et al. a phase i dose-finding, safety and tolerability study of azd8330 in patients with advanced malignancies. eur j cancer 2013,49:1521-1529. |
| ARRY-424704, ARRY-704 Preparation Products And Raw materials |
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