539690 Sigma-AldrichProtein Synthesis Initiation Inhibitor, NSC 119889 - Calbiochem
The Protein Synthesis Initiation Inhibitor, NSC 119889 blocks 5'-mediated/cap-dependent initiation of protein synthesis. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
More>> The Protein Synthesis Initiation Inhibitor, NSC 119889 blocks 5'-mediated/cap-dependent initiation of protein synthesis. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Less<<MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
同义词: 3,4,5,6-Tetrabromofluorescein
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概述
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重要规格表
| Empirical Formula |
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| C₂₀H₈Br₄O₅ |
价格及供货情况
| 产品目录编号 | 库存情况 | 包装 | 数量 / 包装 | 价格 | 数量 | |
|---|---|---|---|---|---|---|
| 539690-25MGCN |
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塑胶安瓿;塑胶针药瓶 | 25 mg |
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| References | |
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| References | Novac, O., et al. 2004. Nucleic Acids Res. 32, 902. Tan, Y.J., et al. 2003. J. Cancer Res. Clin. Oncol. 129, 437. |
| Product Information | |
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| ATP Competitive | N |
| Form | Light brown solid |
| Hill Formula | C₂₀H₈Br₄O₅ |
| Chemical formula | C₂₀H₈Br₄O₅ |
| Reversible | N |
| Structure formula Image | |
| Quality Level | MQ100 |
| Applications |
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| Biological Information | |
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| Primary Target | human arginine methyl transferase |
| Primary Target IC<sub>50</sub> | 1.41 µM against human arginine methyl transferase |
| Purity | ≥95% by HPLC |
| Physicochemical Information | |
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| Cell permeable | Y |
| Dimensions |
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| Materials Information |
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| Toxicological Information |
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| Safety Information according to GHS |
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| Safety Information |
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| Product Usage Statements |
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| Packaging Information |
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| Supplemental Information |
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| Specifications |
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| Global Trade Item Number | |
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| 产品目录编号 | GTIN |
| 539690-25MGCN | 04055977194227 |
Documentation
Protein Synthesis Initiation Inhibitor, NSC 119889 - Calbiochem MSDS
| 职位 |
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Protein Synthesis Initiation Inhibitor, NSC 119889 - Calbiochem 分析证书
| 标题 | 批号 |
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| 539690 |
参考
| 参考信息概述 |
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| Novac, O., et al. 2004. Nucleic Acids Res. 32, 902. Tan, Y.J., et al. 2003. J. Cancer Res. Clin. Oncol. 129, 437. |



