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  • 柴胡皂苷B3

    Saikosaponin B3

    柴胡皂苷B3
    产品编号 CFN80311
    CAS编号 58316-42-0
    分子式 = 分子量 C43H72O14 = 813.02
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The herbs of Bupleurum chinense 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
    柴胡皂苷B3 CFN80311 58316-42-0 1mg QQ客服:1457312923
    柴胡皂苷B3 CFN80311 58316-42-0 5mg QQ客服:1457312923
    柴胡皂苷B3 CFN80311 58316-42-0 10mg QQ客服:1457312923
    柴胡皂苷B3 CFN80311 58316-42-0 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
  • Semmelweis Unicersity (Hungary)
  • Universitas Airlangga (Indonesia)
  • Instytut Nawozów Sztucznych w Pu?awach (Poland)
  • Wroclaw Medical University (Poland)
  • Heinrich-Heine-University Düsseldorf (Germany)
  • Srinakharinwirot University (Thailand)
  • University of Melbourne (Australia)
  • The Ohio State University (USA)
  • Sapienza University of Rome (Italy)
  • Korea Food Research Institute(KFRI) (Korea)
  • Institute of Pathophysiology Medical University of Vienna (Austria)
  • Tohoku University (Japan)
  • Uniwersytet Jagielloński w Krakowie (Poland)
  • University of the Basque Country (Spain)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Clin Med.2019, 8(10):E1664
  • FEMS Microbiol Lett.2017, 364(11)
  • Tumour Biol.2015, 36(12):9385-93
  • Biochem Pharmacol.2017, 130:10-20
  • Metabolites2023, 13(1), 3.
  • Front Pharmacol.2021, 12:690113.
  • Front Cell Dev Biol.2020, 8:32.
  • J Cell Biochem.2022, 123(7):1222-1236.
  • Asian J Beauty Cosmetol2022, 20(2):183-191
  • Biosci Rep.2018, 38(4)
  • J Pharm Biomed Anal.2021, 196:113931.
  • Food Science and Biotechnology2023, 2023:1007
  • J Health Sci Med Res.2023, 31584.
  • Antioxidants.2022, 11(3):491.
  • Nutrients.2020, 12(12):3607.
  • Molecules.2022, 27(22):7997.
  • Evid Based Complement Alternat Med.2018, 2018:1073509
  • National University of Pharmacy2022, 1:73-76
  • Enzyme and Microbial Technology2022, 110002.
  • Int Immunopharmacol.2023, 7:127:111322.
  • JPC-Journal of Planar Chromatography 2017, 30(4)
  • Journal of Physiology & Pathology in Korean Medicine.2018, 32(2): 106-112
  • Plants (Basel).2020, 9(11):1535.
  • ...
  • 生物活性
    Description: Saikosaponin B3 shows some analgesic effect.
    Targets: AChR
    In vitro:
    Molecules. 2014 Dec 4;19(12):20340-9.
    Saikosaponin D isolated from Bupleurum falcatum inhibits selectin-mediated cell adhesion.[Pubmed: 25486247]
    Three saikosaponins were isolated from the MeOH extract of the roots of Bupleurum falcatum L.: Saikosaponin B3 (1);saikosaponin B4 (2); and saikosaponin D (3).
    METHODS AND RESULTS:
    Of the three, compound 3 inhibited the interaction of selectins (E, L, and P) and THP-1 cells with IC50 values of 1.8, 3.0 and 4.3 μM, respectively. Also, the aglycone structure 4 of compound 3 showed moderate inhibitory activity on L-selectin-mediated cell adhesion.
    CONCLUSIONS:
    From these results, we suspect that compound 3 isolated from Bupleurum falcatum roots would be a good candidate for therapeutic strategies to treat inflammation.
    In vivo:
    Journal of pharmacobio-dynamics, 1980, 3(6):269.
    Analgesic and other pharmacologic actions of saikosaponin in repeated cold stressed (SART stressed) animals[Reference: WebLink]
    The pharmacological actions of 7 pure Saikosaponins (a, b1, b2, b3, b4, c and d), the components of Saiko, which plays an important role in Oriental medicine, were studied with special attention to the analgesic effect in repeated cold stressed (SART stressed) mice.
    METHODS AND RESULTS:
    Single administration of 10 mg/kg of Saikosaponin (SS) in normal mice gave no analgesic effect, but the analgesic effect of b2 and c was great in SART stressed mice, and some analgesic effect was noted with Saikosaponin a, Saikosaponin b1, and Saikosaponin B3 in SART stressed mice. Administration of 5 mg/kg/day of SS for 5 days in SART stressed mice gave an intense analgesic effect with b2 and c, and similar administration of a, b1, b3 and b4 also gave some analgesic effect. The inhibition of the body weight increase in SART stressed mice was counteracted in a dose-dependent manner by administration of 2.5-10 mg/kg/day of SSb2 and c for 5 consecutive days, but similar administration of d augmented the inhibition of body weight. The effect of administration of 5 mg/kg/day of SS for 5 days on the decrease of ACh-response in isolated duodenum from SART stressed mice, which were considered to be in partial vagotonia in small intestine, was studied. While Saikosaponin c, Saikosaponin b1, b2, Saikosaponin B3, Saikosaponin a and Saikosaponin b4 were inhibitory, d was entirely ineffective. The effect of administration of SS on the increase of the ACh-response in isolated duodenum from mice stressed by restraint and water immersion, which were considered to be in partial sympathicotonia in small intestine, was also studied. An inhibitory effect was seen with d, which had been without effect in the specimen from SART stressed mice, while no effect of b2, c and a was noted, despite the positive effect in SART stressed mice. Three kinds of SS effects were distinguished, a central stimulating effect, a central inhibitory effect and a negative effect, based on the hypnotic effect on combined use with pentobarbital, result of measurement of motor activities in open field test in normal mice and experiment on electric resistance of the skin by GSR in SART stressed rats.
    CONCLUSIONS:
    According to the above results, particularly effects on the change of ACh-response in isolated duodenum, a classification of the action of SS was attempted.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.23 mL 6.1499 mL 12.2998 mL 24.5996 mL 30.7496 mL
    5 mM 0.246 mL 1.23 mL 2.46 mL 4.9199 mL 6.1499 mL
    10 mM 0.123 mL 0.615 mL 1.23 mL 2.46 mL 3.075 mL
    50 mM 0.0246 mL 0.123 mL 0.246 mL 0.492 mL 0.615 mL
    100 mM 0.0123 mL 0.0615 mL 0.123 mL 0.246 mL 0.3075 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
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    Aglinin A; Aglinin A CFN98268 246868-97-3 C30H50O5 = 490.7 5mg QQ客服:215959384
    5-O-阿魏酰奎尼酸; 5-O-Feruloylquinic acid CFN92889 40242-06-6 C17H20O9 = 368.3 10mg QQ客服:2056216494
    Sahandol; Sahandol CFN96688 1452398-07-0 C20H24O2 = 296.41 5mg QQ客服:215959384

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