化学信息:
中文名 | 杜鹃素 |
英文名 | Farrerol |
中文别名 | - |
英文别名 | - |
来源 | 满山红Rhododendron mariesii Hemsl. et Wils. |
化合物类型 | 黄酮类(Flavonoids)>黄酮>二氢黄酮 |
化学式 | C17H16O5 |
分子量 | 300.31 |
CAS号 | 24211-30-1 |
纯度 | 98%, HPLC |
溶剂/溶解度 | DMSO: 55 mg/ml(183.1 mM); Chloroform, Dichloromethane, Ethyl Acetate, Acetone, etc.: Soluble |
溶液配制 | 5mg加入1.66ml DMSO,或者每3.00mg加入1ml DMSO,配制成10mM溶液。 |
生物信息
产品描述 | Farrerol is a bioactive constituent of Rhododendron, with broad activities such as anti-oxidative, anti-inflammatory, anti-tumor, neuroprotective and hepatoprotective effects. | ||||
信号通路 | Autophagy | ||||
靶点 | AKT | ERK1/2 | JNK1/2 | NF-κB p65 | - |
IC50 | - | - | - | - | - |
体外研究 | Farrerol observably reduces the production of inflammatory mediators including IL-1β, IL-6, TNF-α, COX-2, and iNOS in LPS-induced RAW264.7 cells via suppressing AKT, ERK1/2, JNK1/2, and NF-κB p65 phosphorylation. Farrerol attenuates β-amyloid-induced oxidative stress and inflammation through Nrf2/Keap1 pathway in a microglia cell line. Farrerol inhibits angiogenesis through Akt/mTOR, Erk and Jak2/Stat3 signal pathway. Farrerol overcomes the invasiveness of lung squamous cell carcinoma cells by regulating the expression of inducers of epithelial mesenchymal transition. Farrerol ameliorates acetaminophen-induced hepatotoxicity via activation of Nrf2 and autophagy. | ||||
体内研究 | Farrerol protects dopaminergic neurons in a rat model of lipopolysaccharide-induced Parkinson's disease by suppressing the activation of the AKT and NF-κB signaling pathways. | ||||
临床实验 | N/A |
产品编号 | 产品名称 | 包装 |
SM2093-10mM | 杜鹃素(98%, HPLC) | 10mM×0.2ml |
SM2093-5mg | 杜鹃素(98%, HPLC) | 5mg |
SM2093-25mg | 杜鹃素(98%, HPLC) | 25mg |
SM2093-100mg | 杜鹃素(98%, HPLC) | 100mg |
- | 说明书 | 1份 |
-20℃避光保存,至少一年有效。固体粉末4℃避光保存,至少一个月有效。如果溶于非DMSO溶剂,建议分装后-80℃避光保存,预计6个月内有效。
注意事项:本产品可能对人体有一定的毒害作用,请注意适当防护,以避免直接接触人体或吸入体内。
本产品仅限于专业人员的科学研究用,不得用于临床诊断或治疗,不得用于食品或药品,不得存放于普通住宅内。
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