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  • 紫菀酮

    Shionone

    紫菀酮
    产品编号 CFN99784
    CAS编号 10376-48-4
    分子式 = 分子量 C30H50O = 426.72
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The flowers of Chrysanthemum morifolium
    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
    紫菀酮 CFN99784 10376-48-4 10mg QQ客服:215959384
    紫菀酮 CFN99784 10376-48-4 20mg QQ客服:215959384
    紫菀酮 CFN99784 10376-48-4 50mg QQ客服:215959384
    紫菀酮 CFN99784 10376-48-4 100mg QQ客服:215959384
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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 the Basque Country (Spain)
  • Universidade de Franca (Brazil)
  • University of Eastern Finland (Finland)
  • Korea Food Research Institute(KFRI) (Korea)
  • University of Hertfordshire (United Kingdom)
  • Colorado State University (USA)
  • Utah State University (USA)
  • Ateneo de Manila University (Philippines)
  • Helmholtz Zentrum München (Germany)
  • Heidelberg University (Germany)
  • National Research Council of Canada (Canada)
  • Imperial College London (United Kingdom)
  • Medical University of Gdansk (Poland)
  • Auburn University (USA)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Phytother Res.2022, 10.1002:ptr.7592.
  • Antimicrob Agents Chemother.2024, e0031424.
  • Separations2023, 10(2), 131.
  • Journal of Applied Biology & Biotechnology2023,11(4):148-158
  • Horticulturae2020, 6(4),76.
  • Food Chem.2021, 360:130063.
  • Vietnam J. Chemistry2022, 60(2):211-222
  • Forensic Sci Int.2022, 341:111475.
  • Front Pharmacol.2021, 12:744624.
  • PLoS One.2017, 12(8):e0181191
  • Toxicol In Vitro.2019, 59:161-178
  • J Nat Med.2021, doi: 10.1007.
  • Med Sci Monit.2019, 25:9499-9508
  • Mol Biol Rep.2022, doi: 10.1007
  • Int J Biol Sci.2023, 19(10):3077-3098.
  • University of Stuttgart2021, 11682.
  • Food Science and Biotechnology2023, 2023:1007
  • Fitoterapia.2022, 157:105130.
  • Biosci Rep.2020, 40(8):BSR20201219.
  • Babol University of Medical Sciences2024, rs-4289336
  • Biorxiv.2020, doi: 10.1101.
  • Antioxidants (Basel).2024, 13(3):340.
  • Front. Physiol.2022, 790345.
  • ...
  • 生物活性
    Description: Shionone has anti-inflammatory effect, the mechanism is related to decrease the phosphorylation level of ERK1/2 protein and IκBα and the protein expression of i NOS. It can inhibit the activity of ubiquitin-specific protease 2 (USP2) and provide a lead compound for future development of new USP2 inhibitors.
    Targets: ERK | IkB | NOS | IKK
    In vitro:
    China Journal of Traditional Chinese Medicine & Pharmacy, 2016(4):1430-3.
    Study on anti-inflammatory mechanism of shionone based on NF-κB pathway in vitro.[Reference: WebLink]
    To explore anti-inflammatory effect and mechanism of shionone in vitro.
    METHODS AND RESULTS:
    Lipopolysaccharide(LPS)-activated macrophage cells(RAW264.7) were employed as an inflammatory model, which was intervened by the shionone. After the experiment, Western blot was used to detect the protein expression of p-ERK1/2, IκBαand iNOS on the macrophage cells. Compared with the LPS group, the shionone significantly decreased the protein expression of p-ERK1/2 and i NOS(P0.05) and significantly increased the protein expression of IκBα(P0.05).
    CONCLUSIONS:
    The antiinflammatory mechanism of shionone was related to decrease the phosphorylation level of ERK1/2 protein and IκBα and the protein expression of i NOS.
    In vivo:
    J Ethnopharmacol. 2015 Apr 22;164:328-33.
    Expectorant, antitussive, anti-inflammatory activities and compositional analysis of Aster tataricu[Pubmed: 25701752]
    The root of Aster tataricus L. f., recorded in all versions of Chinese Pharmacopoeia, is a traditional Chinese medicine with the function of dispelling phlegm and relieving cough for more than 2000 years. This study was designed to evaluate the expectorant, antitussive, and anti-inflammatory activities of the root of A. tataricus and to explore the chemical substances responsible for these activities.
    METHODS AND RESULTS:
    The 70% ethanol extract of the root of A. tataricus (RA-70) was divided into three fractions, Fr-0, Fr-50 and Fr-95. They were all orally administrated to the mice to investigate their potential expectorant activities by a tracheal phenol red secretion method. The most effective fraction, together with shionone, was evaluated the expectorant, antitussive and anti-inflammatory activities by the mouse models of phenol red secretion, ammonia-induced cough, and xylene-induced ear swelling. Furthermore, the chemical components of the effective fraction were analyzed and identified by an HPLC-Q-TOF/MS method. Treatment with RA-70, Fr-0 and Fr-50 increased the amount of phenol red secretion by 65.3%, 56.5%, and 76.9%, respectively. Fr-50 was chosen for the further investigation and the results showed that Fr-50 at 40, 80 mg/kg significantly enhanced the phenol red secretion of tracheas, increased the latent period and decreased the frequency of cough and inhibited the ear edema in mice. Shionone at 80 mg/kg showed the trend of enhancing sputum secreting, but had no effect on ammonia-induced cough and xylene-induced ear edema. HPLC-Q-TOF/MS analysis indicated that Fr-50 was mainly composed of 12 caffeoylquinic acids (40.8%, in relative peak area), 7 astersaponins (12.0%) and 13 astins/asterinins (pentapeptides, 26.5%).
    CONCLUSIONS:
    The root of A. tataricus has significant expectorant, antitussive and anti-inflammatory effects. Caffeoylquinic acids, astersaponins, and aster peptides, rather than shionone, may be the main constituents responsible for the expectorant and antitussive activities of A. tataricus and act in a synergistic way.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3435 mL 11.7173 mL 23.4346 mL 46.8691 mL 58.5864 mL
    5 mM 0.4687 mL 2.3435 mL 4.6869 mL 9.3738 mL 11.7173 mL
    10 mM 0.2343 mL 1.1717 mL 2.3435 mL 4.6869 mL 5.8586 mL
    50 mM 0.0469 mL 0.2343 mL 0.4687 mL 0.9374 mL 1.1717 mL
    100 mM 0.0234 mL 0.1172 mL 0.2343 mL 0.4687 mL 0.5859 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
    表木栓醇; Friedelanol CFN98804 5085-72-3 C30H52O = 428.7 5mg QQ客服:1413575084
    表木栓醇; Epifriedelanol CFN99806 16844-71-6 C30H52O = 428.7 20mg QQ客服:1457312923
    表无羁萜乙酸酯; Epifriedelanol acetate CFN98223 2259-07-6 C32H54O2 = 470.8 5mg QQ客服:1457312923
    无羁萜,木栓酮; Friedelin CFN98936 559-74-0 C30H50O = 426.7 10mg QQ客服:1457312923
    29-羟基无羁萜-3-酮; 29-Hydroxyfriedelan-3-one CFN98632 39903-21-4 C30H50O2 = 442.7 5mg QQ客服:215959384
    紫菀酮; Shionone CFN99784 10376-48-4 C30H50O = 426.72 20mg QQ客服:1413575084

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