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  • 牡荆甙

    Agnuside

    牡荆甙
    产品编号 CFN99203
    CAS编号 11027-63-7
    分子式 = 分子量 C22H26O11 = 466.4
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Iridoids
    植物来源 The herbs of Vitex negundo 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
    牡荆甙 CFN99203 11027-63-7 10mg QQ客服:3257982914
    牡荆甙 CFN99203 11027-63-7 20mg QQ客服:3257982914
    牡荆甙 CFN99203 11027-63-7 50mg QQ客服:3257982914
    牡荆甙 CFN99203 11027-63-7 100mg QQ客服:3257982914
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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
  • Centrum Menselijke Erfelijkheid (Belgium)
  • The Ohio State University (USA)
  • Kyoto University (Japan)
  • Universidade Federal de Goias (UFG) (Brazil)
  • Colorado State University (USA)
  • Aarhus University (Denmark)
  • Universita' Degli Studi Di Cagliari (Italy)
  • Srinakharinwirot University (Thailand)
  • Wroclaw Medical University (Poland)
  • Michigan State University (USA)
  • MTT Agrifood Research Finland (Finland)
  • University of Helsinki (Finland)
  • Funda??o Universitária de Desenvolvimento (Brazil)
  • University of Toulouse (France)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Food Chem Toxicol.2023, 176:113802.
  • Food Engineering Progress2019, 23(3)209-216
  • Reprod Toxicol.2020, 96:1-10.
  • Molecules.2019, 24(12):E2286
  • Natural Product Communications2020, doi: 10.1177.
  • Biology (Basel).2020, 9(11):363.
  • Biol Pharm Bull.2023, 46(2):245-256.
  • Braz J Med Biol Res.2021, 54(12):e11183.
  • Mediators Inflamm.2016, 2016:7216912
  • Neurotox Res.2022, 40(6):1937-1947.
  • J Ethnopharmacol.2020, 249:112396
  • Molecules.2016, 21(6)
  • Int J Pharmacol2020, 16:1-9
  • Hum Exp Toxicol.2017, 36(11):1169-1176
  • J Clin Med.2022, 11(13):3662.
  • Chem Res Toxicol. 2022, acs.chemrestox.2c00049.
  • International Food Research Journal2018, 25(6):2560-2571
  • Molecules.2021, 26(9):2802.
  • Int J Mol Sci.2022, 23(11):6172.
  • Phytomedicine.2023, 116:154841.
  • Chem Biol Interact.2018, 283:59-74
  • Reprod Sci.2022,10.1007/s43032-022-01117-4.
  • Biomedicines.2024, 12(3):495.
  • ...
  • 生物活性
    Description: Agnuside has anti-arthritic activity, it also shows inhibition of vascular permeability and leukocyte migration in vivo.It inhibited an array of pro-inflammatory mediators (PGE(2) and LTB(4)) and T-cell-mediated cytokines (IL-2, TNF-α, IFN-γ, IL-4, IL-10, IL-17).
    Targets: TNF-α | PGE | LTB | IL Receptor | IFN-γ
    In vivo:
    Inflamm Res. 2012 Apr;61(4):293-304.
    Anti-arthritic activity of agnuside mediated through the down-regulation of inflammatory mediators and cytokines.[Pubmed: 22228102]
    The purpose of this study was to elucidate the probable mechanism for the anti-arthritic activity of agnuside (AGN), a compound isolated from the leaf extract of Vitex negundo.
    METHODS AND RESULTS:
    The anti-inflammatory activity of AGN within a dose range of 1.56-12.50 mg/kg in normal and adrenalectomized rats was evaluated against different inflammagens. An array of pro-inflammatory mediators (PGE(2) and LTB(4)) and T-cell-mediated cytokines (IL-2, TNF-α, IFN-γ, IL-4, IL-10, IL-17) was assayed using flow cytometry, in arthritic paw tissue homogenate and splenocytes of treated animals. Significant anti-arthritic activity was observed in the polyarthritis test in rats and this was associated with significant suppression of inflammatory mediators and T-cell-mediated cytokines (Th1/Th2). The anti-inflammatory activity in adrenalectomized rats confirmed that the effect of AGN is not mediated by the pituitary-adrenal axis. AGN also showed inhibition of vascular permeability and leukocyte migration in vivo.
    CONCLUSIONS:
    The study suggests the possible development of AGN as a therapeutic agent in the treatment of arthritis by the modulation of the host immune response.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.1441 mL 10.7204 mL 21.4408 mL 42.8816 mL 53.6021 mL
    5 mM 0.4288 mL 2.1441 mL 4.2882 mL 8.5763 mL 10.7204 mL
    10 mM 0.2144 mL 1.072 mL 2.1441 mL 4.2882 mL 5.3602 mL
    50 mM 0.0429 mL 0.2144 mL 0.4288 mL 0.8576 mL 1.072 mL
    100 mM 0.0214 mL 0.1072 mL 0.2144 mL 0.4288 mL 0.536 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
    桃叶珊瑚苷; 杜仲苷; Aucubin CFN98530 479-98-1 C15H22O9 = 346.33 20mg QQ客服:1457312923
    6-O-对羟基苯甲酰基桃叶珊瑚苷; 6-O-p-Hydroxybenzoylaucubin CFN99031 1016987-87-3 C22H26O11 = 466.4 5mg QQ客服:3257982914
    牡荆甙; Agnuside CFN99203 11027-63-7 C22H26O11 = 466.4 20mg QQ客服:2159513211
    10-O-香草酰杜仲甙; 10-O-Vanilloylaucubin CFN99891 193969-08-3 C23H28O12 = 496.5 5mg QQ客服:2159513211
    密力特苷; Melittoside CFN93097 19467-03-9 C21H32O15 = 524.47 20mg QQ客服:2056216494
    地黄苷D; Rhmannioside D CFN90216 81720-08-3 C27H42O20 = 686.61 20mg QQ客服:2159513211

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