| CAS NO: | 34334-69-5 |
| 包装 | 价格(元) |
| 5mg | 电议 |
| 10mg | 电议 |
| 25mg | 电议 |
| 50mg | 电议 |
| 100mg | 电议 |
| 200mg | 电议 |
| 500mg | 电议 |
| 生物活性 | Cirsiliol is a potent and selective5-lipoxygenaseinhibitor and a competitive low affinity benzodiazepine receptor ligand. | ||||||||||||||||
| IC50& Target |
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| 体外研究 (In Vitro) | In concentrations from 0.01 to 300 μM, cirsiliol causes concentration-dependent relaxation of rat isolated ileum. Cirsiliol may inhibit Ca2+influx but stimulates Ca2+release from intracellular stores[1]. Treatment with rhamnetin or cirsiliol reduces the proliferation of NSCLC cells through the suppression of radiation-induced Notch-1 expression[2]. | ||||||||||||||||
| 体内研究 (In Vivo) | In xenograft mouse model, tumor volume is significantly reduced by combinational treatment with irradiation and rhamnetin or cirsiliol compared with irradiation alone[2]. | ||||||||||||||||
| 分子量 | 330.29 | ||||||||||||||||
| 性状 | Solid | ||||||||||||||||
| Formula | C17H14O7 | ||||||||||||||||
| CAS 号 | 34334-69-5 | ||||||||||||||||
| 结构分类 |
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| 来源 |
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| 运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
| 储存方式 | 4°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) | ||||||||||||||||
| 溶解性数据 | In Vitro: DMSO : ≥ 25 mg/mL(75.69 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
