Dehydrocrenatidine
產(chǎn)品名稱:Dehydrocrenatidine
產(chǎn)品描述:
結(jié)構(gòu)類型 | 天然產(chǎn)物 > 生物堿 |
產(chǎn)品描述 | Dehydrocrenatidine is an inhibitor of JAK and induces cell apoptosis. |
體外活性 | In DU145 and MDA-MB-468 cells, Dehydrocrenatidine inhibits cell survival and induces cell apoptosis in a JAK-STAT3-dependent manner. Dehydrocrenatidine reduces the STAT3 phosphorylation stimulated by IL-6, IFN-α, and IFN-γ[1]. Dehydrocrenatidine reduces tetrodotoxin-resistant and sensitive voltage-gated sodium channel currents with IC50 values of 12.36 μM and 4.87 μM, respectively[2]. |
體內(nèi)活性 | Dehydrocrenatidine inhibits voltage-gated sodium channels and ameliorates mechanic allodia in a rat model of neuropathic pain[2]. |
別名 | O-Methylpicrasidine I, Kumujian G |
分子量 | 254.28 |
分子式 | C15H14N2O2 |
CAS No. | 65236-62-6 |
存儲
store at low temperture,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 2 years
溶解度
DMSO: Soluble
( < 1 mg/mL refers to the product slightly soluble or insoluble )
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