Shogaol-6-Shogaol-DataSheet-生命科學(xué)試劑-MedChemExpress

1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEShogaolCat. No.: HY-14616CAS No.: 555-66-8Synonyms: 6-Shogaol; 6-Shogaol分式: CHO分量: 276.37作靶點: Autophagy; Autophagy作通路: Autophagy儲存式: 4C, protect from light* In solvent : -80C, 6 months; -20C, 1 month (protect fromlight)溶解性數(shù)據(jù)體外實驗

2、 DMSO : 50 mg/mL (180.92 mM)* means soluble, but saturation unknown.Mass Solvent1 mg 5 mg 10 mg Concentration制備儲備液1 mM 3.6183 mL 18.0917 mL 36.1834 mL5 mM 0.7237 mL 3.6183 mL 7.2367 mL10 mM 0.3618 mL 1.8092 mL 3.6183 mL請根據(jù)產(chǎn)品在不同溶劑中的溶解度，選擇合適的溶劑配制儲備液，并請注意儲備液的保存式和期限。BIOLOGICAL ACTIVITY物活性 Shogaol (6-Sho

3、gaol)從姜中分離的活性物質(zhì)，具有多種物活性，包括抗癌，抗炎和抗氧化。體外研究Shogaol (6-Shogaol) has anticancer activity against several cell lines 1. Shogaol (6-Shogaol) is identifiedto be cytotoxic in various cell lines, with KB (IC50=7.42.2 M) and HL60 (IC50=7.92.0 M) cells mostsusceptible to 6-shogaol 2. 6-shogaol (IC50=8 M) has mu

4、ch stronger growth inhibitory effects than 6-gingerol (IC50=150 M) on HCT-116 human colon cancer cells 3. Shogaol (6-Shogaol) stimulates1/2 Master of Small Molecules 您邊的抑制劑師www.MedChemEphosphorylations of mitogen-activated protein kinases (MAPKs) such as ERK, JNK, and p38. Moreover, the6-shogaol-ind

5、uced expressions of Nrf2 and HO-1 are attenuated by treatments of SB202190 (a p38 specificinhibitor) and LY294002 (an Akt specific inhibitor) 4.體內(nèi)研究 The Shogaol (6-Shogaol) decreases the diethylnitrosamine (DEN)-mediated elevations of serum aspartatetransaminase and alanine transaminase as well as t

6、he DEN-induced hepatic lipid peroxidation. Inductions ofNrf2 and HO-1 by 6-shogaol are also confirmed in the mice. The administration of Shogaol (6-Shogaol) tothe mice also restores the DEN-reduced activity and protein expression of hepatic antioxidant enzymes suchas superoxide dismutase, glutathion

7、e peroxidase and catalase 4.PROTOCOLCell Assay 4 The effects of 6-shogaol on the viability of HepG2 cells are determined by a MTT assay after 24 h treatment.The data are expressed as percent cell viability compared to that of control. The concentrations of thetreatments 6-shogaol varied from 10 to 1

8、00 g/mL 4.MCE has not independently confirmed the accuracy of these methods. They are for reference only.Animal Mice: Male Balb/c mice are treated with 6-shogaol-rich ginger extracts (10 and 100 mg/kg b.w.) or silymarinAdministration 4 (100 mg/kg b.w.), a positive control, and challenged with diethy

9、l-nitrosoamine (DEN, 30 mg/kg b.w.) 3 daysper week for 3 weeks 4.MCE has not independently confirmed the accuracy of these methods. They are for reference only.戶使本產(chǎn)品發(fā)表的科研獻(xiàn) PLoS Biol. 2018 Jul 12;16(7):e2004921.See more customer validations on HYPERLINK / www.MedChemEREFERENCES1. Semwal RB, et al. Gi

10、ngerols and shogaols: Important nutraceutical principles from ginger. Phytochemistry. 2015 Sep;117:554-68.2. Peng F, et al. Cytotoxic, cytoprotective and antioxidant effects of isolated phenolic compounds from fresh ginger. Fitoterapia. 2012Apr;83(3):568-85.3. Sang S, et al. Increased growth inhibit

11、ory effects on human cancer cells and anti-inflammatory potency of shogaols from Zingiberofficinale relative to gingerols. J Agric Food Chem. 2009 Nov 25;57(22):10645-50.4. Bak MJ, et al. 6-shogaol-rich extract from ginger up-regulated the antioxidant defense systems in cells and mice. Molecules. 2012 Jul4;17(7):8037-55.McePdfHeightCaution: Product has not