513035 Sigma-AldrichPD 158780 - CAS 171179-06-9 - Calbiochem
A potent, cell-permeable, reversible, ATP-competitive inhibitor of the EGFR tyrosine kinase activity (IC₅₀ = 8 pM).
More>> A potent, cell-permeable, reversible, ATP-competitive inhibitor of the EGFR tyrosine kinase activity (IC₅₀ = 8 pM). Less<<PD 158780 - CAS 171179-06-9 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
同义词: 4-[(3-Bromophenyl)amino]-6-(methylamino)-pyrido[3,4-d]pyridimine
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概述
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重要规格表
CAS # | Empirical Formula |
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171179-06-9 | C₁₄H₁₂BrN₅ |
Products
产品目录编号 | 包装 | 数量 / 包装 | |
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513035-500UGCN | 塑胶安瓿;塑胶针药瓶 | 500 μg |
Description | |
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Overview | 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 1/2 (MKK1/2) activation and EGFR tyrosine phosphorylation in HeLa and NIH 3T3 cells. A 10 mM (500 µg/151 µl) solution of PD 158780 (Cat. No. 513036) in DMSO is also available. |
Catalogue Number | 513035 |
Brand Family | Calbiochem® |
Synonyms | 4-[(3-Bromophenyl)amino]-6-(methylamino)-pyrido[3,4-d]pyridimine |
References | |
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References | Cunnick, J.M., et al. 1998. J. Biol. Chem. 273, 14468. Rewcastle, G.W., et al. 1998. J. Med. Chem. 41, 742. |
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CAS number | 171179-06-9 |
ATP Competitive | Y |
Form | Yellow solid |
Hill Formula | C₁₄H₁₂BrN₅ |
Chemical formula | C₁₄H₁₂BrN₅ |
Reversible | Y |
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Quality Level | MQ100 |
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Cell permeable | Y |
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Packaged under inert gas | Packaged under inert gas |
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产品目录编号 | GTIN |
513035-500UGCN | 04055977198645 |
Documentation
PD 158780 - CAS 171179-06-9 - Calbiochem MSDS
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PD 158780 - CAS 171179-06-9 - Calbiochem 分析证书
标题 | 批号 |
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513035 |
参考
参考信息概述 |
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Cunnick, J.M., et al. 1998. J. Biol. Chem. 273, 14468. Rewcastle, G.W., et al. 1998. J. Med. Chem. 41, 742. |