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  • 三七皂苷T5

    Notoginsenoside T5

    三七皂苷T5
    产品编号 CFN92824
    CAS编号 769932-34-5
    分子式 = 分子量 C41H68O12 = 753.0
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The roots of Panax notoginseng (Burk.)F.H.Chen
    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
    三七皂苷T5 CFN92824 769932-34-5 1mg QQ客服:1413575084
    三七皂苷T5 CFN92824 769932-34-5 5mg QQ客服:1413575084
    三七皂苷T5 CFN92824 769932-34-5 10mg QQ客服:1413575084
    三七皂苷T5 CFN92824 769932-34-5 20mg QQ客服:1413575084
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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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  • Charles University in Prague (Czech Republic)
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  • Georgia Institute of Technology (USA)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Biomed Pharmacother.2024, 175:116770.
  • J Cell Physiol.2020, 10.1002
  • Antioxidants (Basel).2020, 9(6):544.
  • Tropical J. of Pha. Research2017, 16(3):543-552
  • Metabolites.2023, 13(6):689.
  • Life Sci.2023, 332:122107.
  • Metabolites.2020, 10(11):440.
  • Molecules.2020, 25(23):5636.
  • Korean J. of Horticultural Sci. & Tech. 2017, 793-804
  • Drug Chem Toxicol.2020, 1-12.
  • Mol Cell.2017, 68(4):673-685
  • Microb Pathog.2024, 189:106609.
  • Horticulturae2024, 10(4), 382.
  • Allergol Immunopathol (Madr).2022, 1;50(4):23-30.
  • Eur J Pharmacol.2024, 963:176280.
  • Biofactors.2018, 44(2):168-179
  • Acta Physiologiae Plantarum2015, 37:1736
  • J Separation Science & Technology2016, 51:1579-1588
  • J Biochem.2024, 175(3):253-263.
  • Free Radic Biol Med.2016, 97:307-319
  • Nutrients2020, 12(2):488
  • Molecules 2022, 27(3),1047.
  • J Appl Microbiol.2022, 132(2):949-963.
  • ...
  • 生物活性
    Description: Total panax notoginsenosides (TPNS) are the main active ingredients in San-Chi, the root of(Burk) F.H. Chen, which belongs to the Araliaceae family and has been used in traditional Chinese medicine to treat atherosclerosis;TPNS can prevent atherosclerosis by lowering serum lipid levels and regulating vascular CD40 and MMP-9 expression, TPNS may have implications for clinical treatment of atherosclerosis vascular disease.
    Targets: MMP(e.g.TIMP)
    In vitro:
    J Ginseng Res . 2018 Jul;42(3):270-276.
    Chemical transformation and target preparation of saponins in stems and leaves of Panax notoginseng[Pubmed: 29983608]
    Abstract Background: Notoginsenoside Ft1 is a promising potential candidate for cardiovascular and cancer disease therapy owing to its positive pharmacological activities. However, the yield of Ft1 is ultralow utilizing reported methods. Herein, an acid hydrolyzing strategy was implemented in the acquirement of rare notoginsenoside Ft1. Methods: Chemical profiles were identified by ultraperformance liquid chromatography coupled with quadruple-time-of-flight and electrospray ionization mass spectrometry (UPLC-Q/TOF-ESI-MS). The acid hydrolyzing dynamic changes of chemical compositions and the possible transformation pathways of saponins were monitored by ultrahigh-performance LC coupled with tandem MS (UHPLC-MS/MS). Results and conclusion: Notoginsenoside Ft1 was epimerized from notoginsenoside ST4, which was generated through cleaving the carbohydrate side chains at C-20 of notoginsenosides Fa and Fc, and vina-ginsenoside R7, and further converted to other compounds via hydroxylation at C-25 or hydrolysis of the carbohydrate side chains at C-3 under the acid conditions. High temperature contributed to the hydroxylation reaction at C-25 and 25% acetic acid concentration was conducive to the preparation of notoginsenoside Ft1. C-20 epimers of notoginsenoside Ft1 and ST4 were successfully separated utilizing solvent method of acetic acid solution. The theoretical preparation yield rate of notoginsenoside Ft1 was about 1.8%, which would be beneficial to further study on its bioactivities and clinical application.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.328 mL 6.6401 mL 13.2802 mL 26.5604 mL 33.2005 mL
    5 mM 0.2656 mL 1.328 mL 2.656 mL 5.3121 mL 6.6401 mL
    10 mM 0.1328 mL 0.664 mL 1.328 mL 2.656 mL 3.3201 mL
    50 mM 0.0266 mL 0.1328 mL 0.2656 mL 0.5312 mL 0.664 mL
    100 mM 0.0133 mL 0.0664 mL 0.1328 mL 0.2656 mL 0.332 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
    20(R)-三七皂苷 R2; 20(R)-Notoginsenoside R2 CFN93373 948046-15-9 C41H70O13 = 771.0 5mg QQ客服:1457312923
    三七皂苷T5; Notoginsenoside T5 CFN92824 769932-34-5 C41H68O12 = 753.0 5mg QQ客服:2159513211
    人参皂苷Rg2; Ginsenoside Rg2 CFN99968 52286-74-5 C42H72O13 = 785.02 20mg QQ客服:2056216494
    人参皂苷Rf; Ginsenoside Rf CFN99976 52286-58-5 C42H72O14 = 801.01 20mg QQ客服:1413575084
    20-葡萄糖人参皂苷R; 20-O-Glucoginsenoside Rf CFN95036 68406-27-9 C48H82O19 = 963.2 5mg QQ客服:1457312923
    (20R)-人参皂苷Rh1; (20R)-Ginsenoside Rh1 CFN92796 80952-71-2 C36H62O9 = 638.9 20mg QQ客服:3257982914
    20R-人参皂苷Rg2; 20R-Ginsenoside Rg2 CFN90412 80952-72-3 C42H72O13 = 785.02 20mg QQ客服:1413575084
    20(S)-原人参三醇; (20S)-Protopanaxatriol CFN90564 34080-08-5 C30H52O4 = 476.4 20mg QQ客服:3257982914
    人参皂苷Rh1; Ginsenoside Rh1 CFN99970 63223-86-9 C36H62O9 = 638.88 20mg QQ客服:1457312923
    三七皂苷R2; Notoginsenoside R2 CFN92364 80418-25-3 C41H70O13 = 771.0 20mg QQ客服:1413575084

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