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(E)-[6]-Dehydroparadol

    
98%

(E)-[6]-Dehydroparadol

源葉(MedMol)
S87005 一鍵復(fù)制產(chǎn)品信息
878006-06-5
C17H24O3
276.3707
貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫存(上海) 北京 武漢 南京 購(gòu)買數(shù)量
S87005-5mg 98% ¥900.00 預(yù)計(jì)交期:2-3天 - - -
S87005-10mg 98% ¥1500.00 預(yù)計(jì)交期:2-3天 - - -
S87005-50mg 98% ¥3800.00 預(yù)計(jì)交期:2-3天 - - -
S87005-100mg 98% ¥4800.00 預(yù)計(jì)交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol (HY-14616), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cells

產(chǎn)品描述: (E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol (HY-14616), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cells
靶點(diǎn): Nrf2
體外研究: (E)-[6]-Dehydroparadol (M15) (5-80 μM; 24 h) inhibits the growth of HCT-116 and H-1299 cells, with IC50s of 43.02 and 41.59 μM, respectively. (E)-[6]-Dehydroparadol (10-40 μM; 24 h) induces apoptosis in HCT-116 and H-1299 cells
體內(nèi)研究: (E)-[6]-Dehydroparadol (compound 19) (5 μM; 24 h) enhances Tg[glutathione S-transferase pi 1 (gstp1):green fluorescent protein (GFP)] fluorescence signal in the Tg(gstp1:GFP) transgenic zebrafish embryos
參考文獻(xiàn): 1. Chen H, et, al. Metabolism of ginger component [6]-shogaol in liver microsomes from mouse, rat, dog, monkey, and human. Mol Nutr Food Res. 2013 May;57(5):865-76. 2. Zhu Y, et, al. Synthesis, evaluation, and metabolism of novel [6]-shogaol derivatives as potent Nrf2 activators. Free Radic Biol Med. 2016 Jun;95:243-54.
溶解性: Soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.618 ml 18.092 ml 36.183 ml
5 mM 0.724 ml 3.618 ml 7.237 ml
10 mM 0.362 ml 1.809 ml 3.618 ml
50 mM 0.072 ml 0.362 ml 0.724 ml
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