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  • 8-姜烯酚

    8-Shogaol

    8-姜烯酚
    产品编号 CFN92299
    CAS编号 36700-45-5
    分子式 = 分子量 C19H28O3 = 304.4
    产品纯度 >=98%
    物理属性 Oil
    化合物类型 Phenols
    植物来源 The rhizomes of Zingber officinale Rosc.
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    8-姜烯酚 CFN92299 36700-45-5 10mg QQ客服:2159513211
    8-姜烯酚 CFN92299 36700-45-5 20mg QQ客服:2159513211
    8-姜烯酚 CFN92299 36700-45-5 50mg QQ客服:2159513211
    8-姜烯酚 CFN92299 36700-45-5 100mg QQ客服:2159513211
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Michigan State University (USA)
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  • Aarhus University (Denmark)
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  • Kitasato University (Japan)
  • Chang Gung University (Taiwan)
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  • Indian Institute of Science (India)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • TCI CO.2019, US20190151257A1
  • J of l. Chroma.&Related Tech2020, 43(11-12):414-423.
  • Pharmaceuticals (Basel).2024 Feb 24;17(3):292.
  • Sci Rep.2015, 5:13194
  • Appl. Sci. 2021, 11(17),7829
  • Applied Biological Chemistry2020, 63:37.
  • Cell Prolif.2021, 54(8):e13083.
  • Foods.2023, 12(19):3647.
  • Int Immunopharmacol. 2020, 83:106403.
  • Foods.2023, 12(6):1227.
  • Molecules.2019, 24(22):E4022
  • J Formos Med Assoc.2020, S0929-6646(20)30425-3
  • Biology (Basel).2020, 9(11):363.
  • International J of Green Pharmacy2019, 13(3)
  • Nutrients.2023, 15(3):753.
  • Biomed Pharmacother.2024, 173:116319.
  • Molecules.2017, 22(12)
  • Biomed Chromatogr.2016, 30(10):1573-81
  • Nutrients2022, 14(14)2929
  • Separations2023, 10(7), 411.
  • Ecol Evol.2022, 12(11):e9459.
  • Biomimetics (Basel).2022, 7(4):154.
  • Front Immunol.2017, 8:1542
  • ...
  • 生物活性
    Description: 8-Shogaol can induce apoptosis in a time- and concentration-dependent manner by reactive oxygen species production and depletion of glutathione in HL-60 cells.
    Targets: ROS
    In vitro:
    Drug Metab Dispos . 2015 Aug;43(8):1181-9.
    Ginsenosides Regulate PXR/NF-κB Signaling and Attenuate Dextran Sulfate Sodium-Induced Colitis[Pubmed: 25986850]
    Abstract Pregnane X receptor (PXR) activation exhibits anti-inflammatory effects via repressing nuclear factor-κB (NF-κB); however, its overactivation may disrupt homeostasis of various enzymes and transporters. Here we found that ginsenosides restore PXR/NF-κB signaling in inflamed conditions without disrupting PXR function in normal conditions. The effects and mechanisms of ginsenosides in regulating PXR/NF-κB signals were determined both in vitro and in vivo. Ginsenosides significantly inhibited NF-κB activation and restored the expression of PXR target genes in tumor necrosis factor-α-stimulated LS174T cells. Despite not being PXR agonists, ginsenosides repressed NF-κB activation in a PXR-dependent manner. Ginsenosides significantly increased the physical association between PXR and the NF-κB p65 subunit and thereby decreased the nuclear translocation of p65. Ginsenoside Rb1 and compound K (CK) were major bioactive compounds in the regulating PXR/NF-κB signaling. Consistently, ginsenosides significantly attenuated dextran sulfate sodium-induced experimental colitis, which was associated with restored PXR/NF-κB signaling. This study indicates that ginsenosides may elicit anti-inflammatory effects via targeting PXR/NF-κB interaction without disrupting PXR function in healthy conditions. Ginsenoside Rb1 and CK may serve as leading compounds in the discovery of new drugs that target PXR/NF-κB interaction in therapy for inflammatory bowel disease.
    In vivo:
    Mol Nutr Food Res. 2013 Mar;57(3):447-58.
    Characterization of thiol-conjugated metabolites of ginger components shogaols in mouse and human urine and modulation of the glutathione levels in cancer cells by [6]-shogaol.[Pubmed: 23322393]
    Shogaols, a series of major constituents in dried ginger with the most abundant being [6]-, [8]-, and [10]-shogaols, show much higher anticancer potencies than gingerols. Previously, we reported the mercapturic acid pathway as a major metabolic route for [6]-shogaol in mice. However, it is still unclear how the side chain length affects the metabolism of shogaols and how shogaols are metabolized in humans.
    METHODS AND RESULTS:
    We first investigate the metabolism of [10]-shogaol in mouse urine, and then investigate the biotransformation of shogaols in human urine. Our results show that eight major thiol-conjugated metabolites of [10]-shogaol were detected in mouse urine, while six major thiol-conjugated metabolites of [6]-shogaol, two thiol-conjugated metabolites of 8-Shogaol, and two thiol-conjugated metabolites of [10]-shogaol were detected in urine collected from human after drinking ginger tea, using LC/ESI-MS/MS. Our results clearly indicate the mercapturic acid pathway is a major metabolic route for [10]-shogaol in mice and for shogaols in human. Furthermore, we also investigated the regulation of glutathione (GSH) by [6]-shogaol in human colon cancer cells HCT-116. Our results show [6]-shogaol, after initially depleting glutathione levels, can subsequently restore and increase GSH levels over time.
    CONCLUSIONS:
    Shogaols are metabolized extensively in mouse and human to form thiol-conjugated metabolites and GSH might play an important role in the cancer-preventive activity of ginger.
    Oxid Med Cell Longev . 2015;2015:843721.
    Ginsenoside Rb1 Treatment Attenuates Pulmonary Inflammatory Cytokine Release and Tissue Injury following Intestinal Ischemia Reperfusion Injury in Mice[Pubmed: 26161243]
    Abstract Objective. Intestinal ischemia reperfusion (II/R) injury plays a critical role in remote organ dysfunction, such as lung injury, which is associated with nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) signaling pathway. In the present study, we tested whether ginsenoside Rb1 attenuated II/R induced lung injury by Nrf2/HO-1 pathway. Methods. II/R injury was induced in male C57BL/6J mice by 45 min of superior mesenteric artery (SMA) occlusion followed by 2 hours of reperfusion. Ginsenoside Rb1 was administrated prior to reperfusion with or without ATRA (all-transretinoic acid, the inhibitor of Nrf2/ARE signaling pathway) administration before II/R. Results. II/R induced lung histological injury, which is accompanied with increased levels of malondialdehyde (MDA), interleukin- (IL-) 6, and tumor necrosis factor- (TNF-) α but decreased levels of superoxide dismutase (SOD) and IL-10 in the lung tissues. Ginsenoside Rb1 reduced lung histological injury and the levels of TNF-α and MDA, as well as wet/dry weight ratio. Interestingly, the increased Nrf2 and HO-1 expression induced by II/R in the lung tissues was promoted by ginsenoside Rb1 treatment. All these changes could be inhibited or prevented by ATRA. Conclusion. Ginsenoside Rb1 is capable of ameliorating II/R induced lung injuries by activating Nrf2/HO-1 pathway.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.2852 mL 16.4258 mL 32.8515 mL 65.703 mL 82.1288 mL
    5 mM 0.657 mL 3.2852 mL 6.5703 mL 13.1406 mL 16.4258 mL
    10 mM 0.3285 mL 1.6426 mL 3.2852 mL 6.5703 mL 8.2129 mL
    50 mM 0.0657 mL 0.3285 mL 0.657 mL 1.3141 mL 1.6426 mL
    100 mM 0.0329 mL 0.1643 mL 0.3285 mL 0.657 mL 0.8213 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    8-姜烯酚; 8-Shogaol CFN92299 36700-45-5 C19H28O3 = 304.4 20mg QQ客服:2056216494
    10-姜烯酚; 10-Shogaol CFN92300 36752-54-2 C21H32O3 = 332.5 20mg QQ客服:1413575084
    6-姜酚; 6-Gingerol CFN99931 23513-14-6 C17H26O4 = 294.4 20mg QQ客服:3257982914
    8-姜酚; 8-Gingerol CFN99131 23513-08-8 C19H30O4 = 322.44 20mg QQ客服:2159513211
    10-姜酚; 10-Gingerol CFN99132 23513-15-7 C21H34O4 = 350.49 20mg QQ客服:2159513211
    1-脱氢-10-姜酮; 1-Dehydro-10-gingerdione CFN92374 136826-50-1 C21H30O4 = 346.5 5mg QQ客服:3257982914
    二乙酰氧基-4-姜二醇; Diacetoxy-4-gingerdiol CFN92373 863780-88-5 C19H28O6 = 352.4 5mg QQ客服:1457312923
    甲基 二乙酰氧基-6-姜二醇; Methyl diacetoxy-6-gingerdiol CFN92301 863780-90-9 C22H34O6 = 394.5 5mg QQ客服:2159513211
    1-脱氢-6-姜酮; 1-Dehydro-6-gingerdione CFN92298 76060-35-0 C17H22O4 = 290.4 10mg QQ客服:2056216494
    6-姜烯酚; 6-Shogaol CFN99531 555-66-8 C17H24O3 = 276.37 20mg QQ客服:1457312923

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