| CAS: | 171179-06-9 | |
| 分子式: | C14H12BrN5 | |
| 分子量: | 330.19 | |
| 沸点: | 499.6°C at 760 mmHg | |
| 熔点: | 174-178°C | |
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||
| P868308 | MACKLIN | N4-(3-溴苯基)-N6-甲基-吡啶并[3,4-D]嘧啶-4,6-二胺 | 97% | 967元/10mg; | 咨询 | ||||||||||||||||||||||||||||||
储存:-20°C 状态:非常淡黄色-黄色晶体-粉末 | |||||||||||||||||||||||||||||||||||
| P2567 | TCI | PD 158780 | >97.0%(HPLC) | 495元/10MG; 1990元/50MG; | 咨询 | ||||||||||||||||||||||||||||||
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| 513035 | Sigma-Aldrich | PD 158780-CAS 171179-06-9-Calbiochem | A potent, cell-permeable, reversible, ATP-competitive inhibitor of the EGFR tyrosine kinase activity (IC₅₀ = 8 pM). | 2741.8元/500 μG; | 咨询 | ||||||||||||||||||||||||||||||
产品说明 一般描述 A potent, cell-permeable, reversible, ATP-competitive inhibitor of the EGFR tyrosine kinase activity (IC50 = 8 pM). Also inhibits heregulin-stimulated autophosphorylation in SK-BR-3 (IC50 = 49 nM) and MDA-MB-453 (IC50 = 52 nM) breast carcinomas. The inhibition is competitive and results from binding of the inhibitor at the ATP site of the enzymes. Inhibits the LPA-stimulated MAP kinase kinase ½ (MKK½) activation and EGFR tyrosine phosphorylation in HeLa and NIH3T3 cells. 包装 500 μg in Plastic ampoule 生化/生理作用 Cell permeable: yes 警告 Toxicity: Standard Handling (A) 重悬 Following reconstitution, aliquot and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C. 其他说明 Cunnick, J.M., et al. 1998. J. Biol. Chem. 273, 14468. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| 461758 | Fluorochem | N4-(3-Bromophenyl)-N6-methylpyrido[3,4-d]pyrimidine-4,6-diamine | 95% | 23870元/250mg; | 咨询 | ||||||||||||||||||||||||||||||
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