| CAS: | 70641-51-9 | ||||
| 分子式: | C27H58NO6P | ||||
| 分子量: | 523.73 | ||||
| 英文名称: |
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| 用途: | 依地福新是一种合成烷基-赖氨磷脂,具有抗肿瘤活性。该化合物诱导多种癌细胞的凋亡。乙二胺嘧啶在细胞膜中积累,在细胞膜中改变脂质成分并诱导脂质筏和 Fas/CD95 死亡受体的共簇。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||
| E920944 | MACKLIN | 依地芬 | ≥95% (HPLC) | 1411元/5mg; | 展开 | ||||||||||||||||||||||||||||||||||||||||
储存:−20°C 状态:固体 | |||||||||||||||||||||||||||||||||||||||||||||
| 341207 | Sigma-Aldrich | ET-18-OCH3-CAS 70641-51-9-Calbiochem | A cell-permeable and reversible cytotoxic agent that shows selective cytocidal activity against neoplastic cells and virally transformed cells. | 1763.65元/5 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A cell-permeable and reversible cytotoxic agent that shows selective cytocidal activity against neoplastic cells and virally transformed cells. Selectively inhibits phosphatidylinositol-specific phospholipase C (PI-PLC, IC50 = 9.6 µM) but does not inhibit phosphatidylcholine-specific PLC or PLD. Inhibits protein kinase C from various leukemic cells. Also promotes rapid and selective apoptosis in human leukemic cells. Has strong antitumor and anticancer properties. 包装 5 mg in Plastic ampoule 生化/生理作用 Cell permeable: yes 注意 Material may form micelles in aqueous stock solutions, which may affect experimental results. 警告 Toxicity: Carcinogenic / Teratogenic (D) 重悬 Following reconstitution in ethanol, aliquot and freeze (-20°C). Ethanol stock solutions are stable for up to 3 months at -20°C. Unstable in aqueous solution; reconstitute just prior to use. 其他说明 Harguindey, J., et al. 2000. Apoptosis5, 87. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
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| SML0332 | Sigma-Aldrich | Edelfosine | ≥95% (HPLC) | 1666.25元/5 MG; 5366.38元/25 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 依地福新具有抗炎、抗自身免疫、抗寄生虫和抗病毒的特性。它通过细胞收缩和细胞膜扰乱来刺激红细胞衰亡。 应用 依地福新已用于治疗人肺癌 A549 细胞,并研究其对 Tuftelin 1(TUFT1)表达的影响。它还用于评估 MCF-7/M 细胞的细胞生长。 包装 5, 25 mg in glass bottle 生化/生理作用 依地福新是一种合成烷基-赖氨磷脂,具有抗肿瘤活性。该化合物诱导多种癌细胞的凋亡。乙二胺嘧啶在细胞膜中积累,在细胞膜中改变脂质成分并诱导脂质筏和 Fas/CD95 死亡受体的共簇。 特点和优势 这种化合物是激酶磷酸酶生物学研究的特色产品。点击此处发现更多特色激酶磷酸酶生物产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。 基本信息
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