| CAS: | 62004-35-7 | ||
| 分子式: | C11H8Br2N2O2 | ||
| 分子量: | 360.01 | ||
| 中文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||
| L868609 | MACKLIN | 2-氰基-N-(2,5-二溴苯基)-3-羟基-2-丁烯酰胺 | 98% | 522元/10mg; 1549元/50mg; | 咨询 | ||||||||||||||||||||||||||||||||
储存:2-8°C 状态:浅棕色固体 | |||||||||||||||||||||||||||||||||||||
| L0309 | TCI | LFM-A13 | >98.0%(HPLC) | 690元/10MG; 1990元/50MG; | 咨询 | ||||||||||||||||||||||||||||||||
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| 435300 | Sigma-Aldrich | LFM-A13-CAS 62004-35-7-Calbiochem | A potent, cell-permeable, reversible, substrate competitive, and specific inhibitor of Bruton′s Tyrosine Kinase (BTK; IC₅₀ = 17.2 µM for human BTK in vitro and IC₅& | 2165.23元/5 MG; | 咨询 | ||||||||||||||||||||||||||||||||
产品说明 一般描述 A potent, cell-permeable, reversible, substrate competitive, and specific inhibitor of Bruton’s Tyrosine Kinase (BTK; IC50 = 17.2 µM for human BTK in vitro and IC50 = 2.5 µM for recombinant BTK). Also inhibits Polo-like kinase in an ATP-competitive manner (IC50 = 10 µM and 61 µM for Plx1 and Plk3, respectively), and displays antitumor properties. Does not affect the enzymatic activity of other protein tyrosine kinases, including EGFR, HCK, IRK JAK1, and JAK3 even at concentrations of 278 µM. Enhances the chemosensitivity of BTK-positive B-lineage leukemia cells to ceramide- and vincristine-induced apoptosis. 包装 5 mg 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 (-20°C). Stock solutions are stable for up to 3 months at -20°C. 其他说明 Uckun, F.M., et al. 2006. Bioorg. Med. Chem. In press. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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