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  • 野马追内酯O

    Eupalinolide O

    野马追内酯O
    产品编号 CFN91839
    CAS编号 2170228-67-6
    分子式 = 分子量 C22H26O8 = 418.4
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Sesquiterpenoids
    植物来源 The herbs of Eupatorium lindleyanum DC.
    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
    野马追内酯O CFN91839 2170228-67-6 1mg QQ客服:1457312923
    野马追内酯O CFN91839 2170228-67-6 5mg QQ客服:1457312923
    野马追内酯O CFN91839 2170228-67-6 10mg QQ客服:1457312923
    野马追内酯O CFN91839 2170228-67-6 20mg QQ客服:1457312923
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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
  • University of Brasilia (Brazil)
  • Utrecht University (Netherlands)
  • Florida A&M University (USA)
  • University of British Columbia (Canada)
  • National Chung Hsing University (Taiwan)
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
  • Universidad Miguel Hernández (Spain)
  • University of Toronto (Canada)
  • Florida International University (USA)
  • Siksha O Anusandhan University (India)
  • Complutense University of Madrid (Spain)
  • Universite Libre de Bruxelles (Belgium)
  • University of Mysore (India)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Int Immunopharmacol.2019, 71:22-31
  • Sci Rep.2017, 7(1):3249
  • Antiviral Res.2021, 193:105142.
  • Int J Mol Sci.2020, 21(9):3144.
  • J Appl Biol Chem2022, 65:343−348.
  • Oncol Rep.2019, 41(4):2453-2463
  • Eur J Pharmacol.2021, 899:174010.
  • Drug Chem Toxicol.2024, 1-10.
  • Oncol Rep.2021, 46(2):166.
  • Antioxidants (Basel).2022, 11(1):171.
  • Molecules.2022, 27(22):7997.
  • Molecules.2023, 28(8):3503.
  • J Cell Physiol.2021, 236(3):1950-1966.
  • Int J Mol Sci.2021, 22(21):11836.
  • J Ethnopharmacol.2017, 209:305-316
  • Chemistr of plant2016, 2016021195
  • ACS Nano.2018, 12(4):3385-3396
  • J Chromatogr A.2024, 1714:464544.
  • Biofactors.2018, 44(2):168-179
  • Antioxidants (Basel).2022, 11(12):2496.
  • J Food Biochem.2021, 45(7):e13774.
  • Antioxidants (Basel).2020, 9(2): E119
  • Pharmacol Res.2020, 161:105205.
  • ...
  • 生物活性
    Description: Eupalinolide O shows significant anticancer activity, it induces cell cycle arrest and apoptosis in human MDA-MB-468 breast cancer cells.
    Targets: Akt
    In vitro:
    Nat Prod Res,2019 Feb;33(4):477-485.
    Precise discovery of a STAT3 inhibitor from Eupatorium lindleyanum and evaluation of its activity of anti-triple-negative breast cancer.[Pubmed: 29086600]
    Michael reaction acceptors (MRAs) are a class of active compounds. There is a great prospect to screen STAT3 inhibitors from Eupatorium lindleyanum, furthermore, to discover lead compounds for anti-triple-negative breast cancer (TNBC).
    METHODS AND RESULTS:
    In this study, glutathione (GSH) was employed, and a UPLC-MS screening method was developed to discover MRAs. We screened MRAs which can inhibit STAT3 using a STAT3-dependent reporter system. Six sesquiterpene lactones, including a new compound Eupalinolide O (1), together with five known compounds, Eupalinolide I (2), Eupalinolide K (3), Eupalinolide H (4), Eupalinolide J (5) and Eupalinolide G (6) were isolated. Eupalinolide J was identified as MRA that decreased luciferase activity of STAT3. Preliminary activity assessment showed that Eupalinolide J could inhibit the viability of TNBC cell lines.
    CONCLUSIONS:
    We demonstrated that Eupalinolide J, which is a natural typical MRA, has a notable inhibition of STAT3 activity and a potential cytotoxic activity against TNBC cell lines.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3901 mL 11.9503 mL 23.9006 mL 47.8011 mL 59.7514 mL
    5 mM 0.478 mL 2.3901 mL 4.7801 mL 9.5602 mL 11.9503 mL
    10 mM 0.239 mL 1.195 mL 2.3901 mL 4.7801 mL 5.9751 mL
    50 mM 0.0478 mL 0.239 mL 0.478 mL 0.956 mL 1.195 mL
    100 mM 0.0239 mL 0.1195 mL 0.239 mL 0.478 mL 0.5975 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
    Carabrolactone A; Carabrolactone A CFN99286 1187925-30-9 C15H22O5 = 282.3 5mg QQ客服:1413575084
    11(13)-去氢腋生依瓦菊素; 11(13)-Dehydroivaxillin CFN97438 87441-73-4 C15H20O4 = 264.3 5mg QQ客服:1413575084
    Aeruginolactone; Aeruginolactone CFN92791 1005208-88-7 C15H20O3 = 248.3 5mg QQ客服:1413575084
    野马追内酯O; Eupalinolide O CFN91839 2170228-67-6 C22H26O8 = 418.4 5mg QQ客服:2159513211
    野马追内酯A; Eupalinolide A CFN90381 877822-41-8 C24H30O9 = 462.49 20mg QQ客服:215959384
    野马追内酯B; Eupalinolide B CFN90382 877822-40-7 C24H30O9 = 462.49 20mg QQ客服:1413575084
    野马追内酯K; Eupalinolide K CFN99435 108657-10-9 C20H26O6 = 362.4 10mg QQ客服:1413575084
    4,15-Isoatriplicolide methylacrylate; 4,15-Isoatriplicolide methylacrylate CFN92956 133559-38-3 C19H20O6 = 344.36 5mg QQ客服:1413575084
    Isoatriplicolide tiglate; Isoatriplicolide tiglate CFN92955 133559-39-4 C20H22O6 = 358.39 5mg QQ客服:1457312923

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