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  • 7,8-二羟基升麻醇

    7,8-Didehydrocimigenol

    7,8-二羟基升麻醇
    产品编号 CFN92381
    CAS编号 150972-72-8
    分子式 = 分子量 C30H46O5 = 486.7
    产品纯度 >=98%
    物理属性 Cryst.
    化合物类型 Triterpenoids
    植物来源 The roots of Cimicifuga foetida L.
    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
    7,8-二羟基升麻醇 CFN92381 150972-72-8 1mg QQ客服:2159513211
    7,8-二羟基升麻醇 CFN92381 150972-72-8 5mg QQ客服:2159513211
    7,8-二羟基升麻醇 CFN92381 150972-72-8 10mg QQ客服:2159513211
    7,8-二羟基升麻醇 CFN92381 150972-72-8 20mg 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
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  • Leibniz Institute of Plant Biochemistry (Germany)
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  • Deutsches Krebsforschungszentrum (Germany)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Tumour Biol.2015, 36(9):7027-34
  • J Nat Med.2022, 76(1):59-67.
  • Molecules.2018, 23(9):E2121
  • LWT-Food Sci Technol2020, 109163
  • Plants (Basel).2022, 11(16):2126.
  • Phytomedicine.2024, 122:155065.
  • Industrial Crops and Products2020, 146:112186
  • Sci Rep.2019, 9(1):4646
  • Curr Issues Mol Biol.2022, 44(5):2300-2308.
  • Compounds.2023, 3(1), 169-179.
  • Pharm Biol.2022, 60(1):2040-2048.
  • Industrial Crops and Products2023, 199:116746.
  • Processes2021, 9(1), 153.
  • Tissue Cell.2022, 78:101901.
  • Pathogens.2018, 7(3):E62
  • BMC Complement Altern Med.2016, 16:213
  • Journal of Chromatography A2020, 460942
  • J Sep Sci.2018, 41(7):1682-1690
  • QASCF2022, 14(4).
  • Mediators Inflamm.2016, 2016:7216912
  • The Japan Society for Analy. Chem.2017, 66(8):613-617
  • Int J Mol Sci.2021, 22(14):7324.
  • Plants (Basel).2021, 10(11):2525.
  • ...
  • 生物活性
    Description: 7,8-Didehydrocimigenol can be used for the treatment of cardiovascular disorders such as atherosclerosis. It upregulates PPAR-γ in EC inhibits NF-kB activity of TNF-α-activated EC which leads to selective inhibition of VCAM-1 expression.
    Targets: TNF-α | PPAR | NF-kB | ERK | Akt | IkB | IKK
    In vitro:
    Food Chem Toxicol. 2011 Jan;49(1):166-72.
    7,8-didehydrocimigenol from Cimicifugae rhizoma inhibits TNF-α-induced VCAM-1 but not ICAM-1expression through upregulation of PPAR-γ in human endothelial cells.[Pubmed: 20946932]
    Activators of PPAR have been demonstrated to inhibit the induction of VCAM-1 but not ICAM-1 in human endothelial cells (EC). During the screening of anti-inflammatory activity of traditional herbs, we found 7,8-Didehydrocimigenol (7,8-DHC), one of active triterpenoids of Cimicifugae rhizoma (C. rhizoma) increases PPAR-γ expression in EC in a time- and dose-dependent manner.
    METHODS AND RESULTS:
    Therefore, we asked whether 7,8-Didehydrocimigenol selectively inhibits the expression of VCAM-1 but not ICAM-1 in TNF-α-activated EC via upregulation of PPAR-γ. Treatment with 7,8-Didehydrocimigenol or PPAR-γ agonists (GW1929, troglitazone) inhibited the expression of VCAM-1 but not ICAM-1. 7,8-Didehydrocimigenol significantly inhibited NF-kB activity via inhibition of phosphorylation of IkB and it also inhibited phosphorylation of ERK1/2 and Akt but not PKC. Finally, attachment of monocytes (U937) to EC by TNF-α was significantly reduced by 7,8-Didehydrocimigenol .
    CONCLUSIONS:
    These results indicate that upregualtion of PPAR-γ by 7,8-Didehydrocimigenol in EC inhibits NF-kB activity of TNF-α-activated EC which leads to selective inhibition of VCAM-1 expression. In addition, ERK1/2 and Akt signal pathways are involved in differential regulation by 7,8-Didehydrocimigenol. We concluded that 7,8-Didehydrocimigenol can be used for the treatment of cardiovascular disorders such as atherosclerosis.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.0547 mL 10.2733 mL 20.5465 mL 41.0931 mL 51.3663 mL
    5 mM 0.4109 mL 2.0547 mL 4.1093 mL 8.2186 mL 10.2733 mL
    10 mM 0.2055 mL 1.0273 mL 2.0547 mL 4.1093 mL 5.1366 mL
    50 mM 0.0411 mL 0.2055 mL 0.4109 mL 0.8219 mL 1.0273 mL
    100 mM 0.0205 mL 0.1027 mL 0.2055 mL 0.4109 mL 0.5137 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
    24-epi-24-O-acetyl-7,8-didehydrohydroshengmanol-3-O-beta-D-xylopyranoside; 24-epi-24-O-acetyl-7,8-didehydrohydroshengmanol-3-O-beta-D-xylopyranoside CFN95628 228251-25-0 C37H58O11 = 678.9 5mg QQ客服:2159513211
    7,8-二羟基升麻醇; 7,8-Didehydrocimigenol CFN92381 150972-72-8 C30H46O5 = 486.7 5mg QQ客服:1457312923
    升麻酮; Cimigenol-3-one CFN89138 31222-32-9 C30H46O5 = 486.69 5mg QQ客服:2056216494
    升麻苷E; Cimiside E CFN92974 154822-57-8 C35H54O8 = 602.80 5mg QQ客服:2056216494
    25-脱氢升麻醇 3-O-beta-D-木糖苷; 25-Anhydrocimigenol 3-O-beta-D-xyloside CFN92522 181765-11-7 C35H54O8 = 602.8 5mg QQ客服:3257982914
    24-表-7,8-二羟基升麻醇 3-O-木糖苷; 24-epi-7,8-Didehydrocimigenol 3-xyloside CFN95627 150972-77-3 C35H54O9 = 618.8 5mg QQ客服:3257982914
    升麻环氧醇苷; Cimigenoside CFN98340 27994-11-2 C35H56O9 = 620.8 20mg QQ客服:3257982914
    升麻酮醇 3-O-alpha-L-拉伯糖苷; Cimiracemoside C CFN98288 256925-92-5 C35H56O9 = 620.8 10mg QQ客服:215959384
    升麻苷B; Cimiside B CFN99637 152685-91-1 C40H64O13 = 752.9 5mg QQ客服:2056216494
    Cimiracemoside D; Cimiracemoside D CFN90649 290821-39-5 C37H58O11 = 678.39 10mg QQ客服:3257982914

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