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  • 甘草皂苷A3

    Licoricesaponin A3

    甘草皂苷A3
    产品编号 CFN92923
    CAS编号 118325-22-7
    分子式 = 分子量 C48H72O21 = 985.07
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The roots of Glycyrrhiza uralensis
    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
    甘草皂苷A3 CFN92923 118325-22-7 1mg QQ客服:1413575084
    甘草皂苷A3 CFN92923 118325-22-7 5mg QQ客服:1413575084
    甘草皂苷A3 CFN92923 118325-22-7 10mg QQ客服:1413575084
    甘草皂苷A3 CFN92923 118325-22-7 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
    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
  • National Chung Hsing University (Taiwan)
  • Sanford Burnham Prebys Medical Discovery Institute (USA)
  • Charles University in Prague (Czech Republic)
  • University of Indonesia (Indonesia)
  • Sapienza University of Rome (Italy)
  • Kazusa DNA Research Institute (Japan)
  • Copenhagen University (Denmark)
  • Universiti Sains Malaysia (Malaysia)
  • Medical University of South Carolina (USA)
  • Florida International University (USA)
  • Imperial College London (United Kingdom)
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  • University of British Columbia (Canada)
  • Chang Gung University (Taiwan)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Talanta.2023, 262:124690.
  • J Med Chem.2023, 66(6):4106-4130.
  • Antioxidants (Basel).2024, 13(3):340.
  • Plants (Basel).2020, 9(11):1535.
  • Journal of Chromatography A2020, 460942
  • J Pharmaceut Biomed2020, 178:112894
  • Int J Mol Sci.2022, 23(13):7115.
  • Horticulture Research2022, uhac276.
  • Journal of Functional Foods2022, 91:105019.
  • J of the Korean Society of Cosmetics and Cosmetology2018, 399-406
  • Asian J Beauty Cosmetol2020, 18(3): 265-272.
  • J of the Society of Cosmetic Scientists of Korea2018, 44(4):407-417
  • Mie University2019, 10076.
  • J Sep Sci.2023, 46(16):e2300160.
  • Russian Journal of Bioorganic Chemistry2023, 49:1689–1698.
  • Plant Pathology2022, 13527
  • J Korean Soc Food Sci Nutr2020, doi: 10.3746.
  • Int J Cosmet Sci.2022, doi:10.1111/ics.12827.
  • Int J Mol Sci.2020, 21(9):3392.
  • Phytochem Anal.2022, doi: 10.1002
  • VNU Journal of Science: Med.& Pharm. Sci.2022, 38(2):2588-1132.
  • Plants (Basel).2024, 13(6):868.
  • Microbiol. Biotechnol. Lett.2022, 50(2): 193-201.
  • ...
  • 生物活性
    Description: Licoricesaponin A3 shows the cytotoxic activity against the human cancer cell lines MGC-803, SW620, and SMMC-7721 with IC50 > 100 μmol/L.
    In vitro:
    Chinese Traditional & Herbal Drugs, 2013, 44(12):1552-1557.
    Chemical constituents of triterpenoid saponins from Glycyrrhiza uralensis.[Reference: WebLink]
    To study the chemical constituents from the roots and rhizomes of Glycyrrhiza uralensis.
    METHODS AND RESULTS:
    The compounds were separated and purified by solvent and chromatographic methods. Their structures were identified by spectroscopic techniques. Fourteen triterpenoid saponins isolated from 50% ethanol extract of the roots and rhizomes of G. uralensis were identified as uralsaponin C (1), uralsaponin D (2), Licoricesaponin A3 (3), uralsaponin F (4), 22β-acetoxyl-glycyrrizin (5), 24-hydroxyl-licorice-saponin E2 (6), licorice-saponin E2 (7), licorice-saponin G2 (8), 22β-acetoxyl-glyrrhaldehyde (9), 3β-O-[β-D-glucuronopyranosyl-(1→2) - β-D-glucuronopyranosyl]-glycyrretol (10), araboglycyrrhizin (11), licorice-saponin J2 (12), glycyrrhizin (13), and glycyrrhetic acid monoglucuronide (14). Compounds 1-14 showed the cytotoxic activity against the human cancer cell lines MGC-803, SW620, and SMMC-7721 with IC50 > 100 μmol/L. The aglycones of compounds 2, 6-8, and 13 displayed the inhibition on the growth of cancer cells with IC50 at 18.3-41.6 μmol/L.
    CONCLUSIONS:
    Compound 14 is a new natural product, and compound 11 is isolated from the plant for the first time; Compounds 1-14 show no cytotoxic activity against the human cancer cell lines MGC-803, SW620, and SMMC-7721, and the aglycones of compounds 2, 6-8, and 13 could significantly increase the cytotoxic activity after hydrolysis.
    Arch Pharm Res. 2012 Nov;35(11):1945-52.
    Comparative study of bioactive constituents in crude and processed Glycyrrhizae radix and their respective metabolic profiles in gastrointestinal tract in vitro by HPLC-DAD and HPLC-ESI/MS analyses.[Pubmed: 23212636]

    METHODS AND RESULTS:
    Two HPLC methods with diode array detection (HPLC-DAD) and electrospray ionization-mass spectrometry (HPLC-ESI/MS), respectively, were developed to investigate the differences of chemical constituents and their metabolism in gastrointestinal tract in vitro between two decoctions of crude and processed Glycyrrhizae radix. Total of eleven constituents (liquiritin apioside, liquiritin, licuraside, isoliquiritin, ononin, glycyrrhizin, liquiritigenin-7,4'-diglucoside, Licoricesaponin A3, 22β-acetoxylglycyrrhizic acid, licorice saponin G2, and yunganoside E2) were identified in the two decoctions, whereas lower contents of these constituents were usually found in the decoction of processed Glycyrrhizae Radix. [corrected] Furthermore, these constituents were metabolized into their respective aglycons in human intestinal bacteria juice, and the metabolism ratios were all higher in processed Glycyrrhizae Radix [corrected] decoction. No change was found in artificial gastric or intestinal juice.
    CONCLUSIONS:
    This study revealed that the processing can alter the contents of main constituents in crude G. radix and their metabolism in gastrointestinal tract, in which intestinal bacteria play an important role in the metabolism of licorice constituents.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.0152 mL 5.0758 mL 10.1516 mL 20.3031 mL 25.3789 mL
    5 mM 0.203 mL 1.0152 mL 2.0303 mL 4.0606 mL 5.0758 mL
    10 mM 0.1015 mL 0.5076 mL 1.0152 mL 2.0303 mL 2.5379 mL
    50 mM 0.0203 mL 0.1015 mL 0.203 mL 0.4061 mL 0.5076 mL
    100 mM 0.0102 mL 0.0508 mL 0.1015 mL 0.203 mL 0.2538 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
    商陆皂苷辛; Esculentoside H CFN90657 66656-92-6 C48H76O21 = 989.1 20mg QQ客服:1413575084
    商陆皂苷T; Esculentoside T CFN90658 N/A C42H64O16 = 824.4 20mg QQ客服:3257982914
    百两金素A; Ardisiacrispin A CFN90177 23643-61-0 C52H84O22 = 1061.21 5mg QQ客服:1457312923
    百两金皂苷B; Ardisiacrispin B CFN91120 112766-96-8 C53H86O22 = 1075.3 5mg QQ客服:2056216494
    朱砂根皂苷A; Ardisicrenoside A CFN91122 160824-52-2 C53H88O22 = 1077.3 5mg QQ客服:3257982914
    单葡萄糖醛酸甘草次酸; Glycyrrhetic acid 3-O-mono-beta-D-glucuronide CFN90683 34096-83-8 C36H54O10 = 646.8 5mg QQ客服:1457312923
    甘草皂苷H2; Licoricesaponin H2 CFN95173 118441-85-3 C42H62O16 = 822.92 20mg QQ客服:2056216494
    甘草酸; Glycyrrhizic acid CFN99151 1405-86-3 C42H62O16 = 822.92 20mg QQ客服:3257982914
    甘草酸铵; Glycyrrhizic acid ammonium salt CFN99153 53956-04-0 C42H65NO16 = 839.96 20mg QQ客服:2159513211
    甘草酸甲酯; Methyl glycyrrhizate CFN91679 104191-95-9 C43H64O16 = 837.0 5mg QQ客服:1457312923

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