木犀草素
面议
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分子式 C15H10O6 分子量286.24 Beilstein号 292084 EC号 207-741-0 MDL号 MFCD00017309 PubChem编号 24896520 属性 熔点 330°C 溶解性 Soluble in a
| 货号 | CAS号 | 价格 | 操作 |
|---|---|---|---|
| L107329-100g | 491-70-3 | 面议 | 询底价 |
| L107329-25g | 491-70-3 | 面议 | 询底价 |
| L107329-1g | 491-70-3 | 面议 | 询底价 |
| L107329-500mg | 491-70-3 | 面议 | 询底价 |
| L107329-5g | 491-70-3 | 面议 | 询底价 |
耗材描述
- 分子式 C15H10O6
- 分子量286.24
- Beilstein号 292084
- EC号 207-741-0
- MDL号 MFCD00017309
- PubChem编号 24896520
属性
| 熔点 | 330°C |
| 溶解性 | Soluble in aqueous alkaline solutions (1.4 mg/ml), ethanol (~5 mg/ml), DMSO (7 mg/ml), 1eq. NaOH (5 mM), DMF (~20 mg/ml), 1:5 solution of DMF:PBS(pH7.2) (`~1 mg/ml), water (1 mg/ml) at 25 °C, and methanol. |
| 存贮条件 | 贮存温度2-8℃ |
| 密度 | 1.6540 |
描述
| 应用 | An inhibitor of glutathione S-transferase and 15-LO. |
| 产品介绍 | Luteolin is an antioxidant flavonoid and a free radical scavenger. It inhibits rat liver cytosolic glutathione S-transferase activity and soybean and reticulocyte 15-LO (15-lipoxygenases). Luteolin also shows cytotoxic effects on Raji lymphoma cells. Incubation of the non-tumor cell line C3H10T?CL8 with luteolin results in induction of p53 accumulation and apoptosis, with apoptosis occurring at the G2/M phase of the cell cycle. Luteolin is an inhibitor of Cot, PDE1-5, c-Src, HDAC, Maltase-glucoamylase, Topo I, PKC ε, Fatty Acid Synthase, PPAR γ and MMP. |
| 别名 | 木犀草素;3',4',5,7-四羟基黄酮，黄色黄素，黄示灵，藤黄菌素3',4',5,7-Tetrahydroxyflavone |
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