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  • 槐角苷

    Sophoricoside

    槐角苷
    产品编号 CFN90148
    CAS编号 152-95-4
    分子式 = 分子量 C21H20O10 = 432.38
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Flavonoids
    植物来源 The fruits of Sophora japonica 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
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    槐角苷 CFN90148 152-95-4 10mg QQ客服:1413575084
    槐角苷 CFN90148 152-95-4 20mg QQ客服:1413575084
    槐角苷 CFN90148 152-95-4 50mg QQ客服:1413575084
    槐角苷 CFN90148 152-95-4 100mg 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
  • University of Hull (United Kingdom)
  • Medical University of South Carolina (USA)
  • Monash University Malaysia (Malaysia)
  • Martin Luther University of Halle-Wittenberg (Germany)
  • Chulalongkorn University (Thailand)
  • University of Illinois (USA)
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  • Florida International University (USA)
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  • Shanghai University of TCM (China)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Front Neurosci.2019, 13:1091
  • Journal of Mushroom2023, 21(4):215-221.
  • European Journal of Integrative Medicine2018, 20:165-172
  • Biochem Biophys Res Commun.2017, 494(3-4):587-593
  • Biomed Pharmacother.2021, 139:111585.
  • Biomed Chromatogr.2020, e5021.
  • Plant Biotechnology Reports 2021, 15:117-124.
  • Sci Rep.2016, 6:25094
  • Molecules 2021, 26(4),1092.
  • Exp Biol Med (Maywood).2019, 244(16):1463-1474
  • J Vet Sci.2020, 21(3):e39.
  • J Chromatogr A.2024, 1714:464544.
  • Exp Mol Med.2020, 52(4):629-642.
  • Molecules.2019, 24(11):E2044
  • Proc Biol Sci.2024, 291(2015):20232578.
  • Life (Basel).2021, 11(12):1399.
  • J Chromatogr B Analyt Technol Biomed Life Sci.2019, 1126-1127:121743
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  • Fitoterapia.2024, 175:105958.
  • J Biol Chem.2021, 297(6):101362.
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  • ...
  • 生物活性
    Description: Sophoricoside has anti-inflammatory, anti-cancer, anti-bone loss, and immunosuppressive effects. Sophoricoside is an effective regulator of lipogenesis and glucose consumption and may find utility in the treatment of obesity and type 2 diabetes. Sophoricoside exposure reduced the number of implanted embryos in a dose-dependent manner and failed the embryo implantation through altering the morphology of uterine and compromising the endometrial receptivity.
    Targets: NF-kB | Caspase | MMP(e.g.TIMP) | Estrogen receptor | COX | IL Receptor | TNF-α | Progestogen receptor
    In vitro:
    Molecules. 2013 Dec 13;18(12):15624-35.
    Modulation of lipogenesis and glucose consumption in HepG2 cells and C2C12 myotubes by sophoricoside.[Pubmed: 24352018]
    Sophoricoside, an isoflavone glycoside isolated from Sophora japonica (Leguminosae), has been widely reported as an immunomodulator. In this study, the effects of sophoricoside on lipogenesis and glucose consumption in HepG2 cells and C2C12 myotubes were investigated.
    METHODS AND RESULTS:
    Treatment with sophoricoside at concentrations of 1-10 μM inhibited lipid accumulation in HepG2 cells in a dose-dependent manner. At the same concentration range, no effect on cell viability was observed in the MTT assay. Inhibition of lipogenesis was associated with the downregulation of SREBP-1a, SREBP-1c, SREBP-2 and their downstream target genes (FAS, ACC, HMGR) as revealed by realtime quantitative PCR. The lipid-lowering effect was mediated via the phosphorylation of AMPK. Further investigation of the activities of this isoflavone showed that sophoricoside has the capability to increase glucose uptake by C2C12 myotubes. It also effectively inhibited the activities of α-glucosidase and α-amylase in vitro and remarkably lowered postprandial hyperglycaemia in starch-loaded C57BL6/J mice.
    CONCLUSIONS:
    These results suggest that sophoricoside is an effective regulator of lipogenesis and glucose consumption and may find utility in the treatment of obesity and type 2 diabetes.
    World J Microbiol Biotechnol. 2015 Jan;31(1):187-97.
    Effective bioconversion of sophoricoside to genistein from Fructus sophorae using immobilized Aspergillus niger and Yeast.[Pubmed: 25392205]
    In this study, sophoricoside from Fructus sophorae was highly bioconversed to genistein by co-immobilized Aspergillus niger and Yeast.
    METHODS AND RESULTS:
    Bioconversion conditions for genistein were optimized with single-factor experiments. The optimal conditions were as follows: microbial concentration 1.5 × 10(7) cells/mL, wet weight of microorganisms beads 10.0 g/g material, pH 5, ratio of liquid to solid 25:1 (mL/g), temperature 32 °C and time 24 h. Under these conditions, a 34.45-fold increase in production of genistein was observed with a bioreactor. Moreover, the antioxidant activities of the extracts from the fermented and untreated F. sophorae were 0.287 ± 0.11, 0.384 ± 0.08 mg/mL (IC50) and 1.84 ± 0.13, 1.28 ± 0.25 mmol Fe(II)/g, according to the DPPH test and FRAP assay, respectively.
    CONCLUSIONS:
    The results indicated that the method described in the current work were valuable procedure for the production of genistein, which is of most importance for industrial scale applications as well as food industry.
    In vivo:
    Chem Biol Interact. 2014 Aug 5;219:57-63.
    Sophoricoside fails the embryo implantation by compromising the uterine endometrial receptivity at implantation [Pubmed: 24877640 ]
    Sophoricoside (SOPH) is an isoflavone glycoside isolated from the fruits of Sophora japonica. Since its first isolation in 1961, there are rare findings about the effects of SOPH on reproductive system.
    METHODS AND RESULTS:
    In the present study, the pregnant mice administrated by different doses of SOPH were used to explore the effect of SOPH on embryo implantation, especially on the endometrial receptivity. The statistical results showed that the number of implanted embryos was gradually declining along the increasing dose of SOPH. When the administrated dose of SOPH was 600 mg/kg per day, great changes were observed in the exposed uterine morphology and up-regulated progesterone receptor (PR) and down-regulated estrogen receptor α (ERα), E-cadherin, matrix metalloproteinase-2 (MMP-2) and integrin β3 were also found in SOPH-exposed uterine.
    CONCLUSIONS:
    These findings demonstrated that SOPH exposure reduced the number of implanted embryos in a dose-dependent manner and failed the embryo implantation through altering the morphology of uterine and compromising the endometrial receptivity.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3128 mL 11.5639 mL 23.1278 mL 46.2556 mL 57.8195 mL
    5 mM 0.4626 mL 2.3128 mL 4.6256 mL 9.2511 mL 11.5639 mL
    10 mM 0.2313 mL 1.1564 mL 2.3128 mL 4.6256 mL 5.782 mL
    50 mM 0.0463 mL 0.2313 mL 0.4626 mL 0.9251 mL 1.1564 mL
    100 mM 0.0231 mL 0.1156 mL 0.2313 mL 0.4626 mL 0.5782 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
    6″-O-木糖黄豆黄苷; 6''-O-xylosyl-glycitin CFN80151 231288-18-9 C27H30O14 = 578.16 5mg QQ客服:2159513211
    Odoratin-7-O-beta-D-glucopyranoside; Odoratin-7-O-beta-D-glucopyranoside CFN91882 210413-47-1 C23H24O11 = 476.43 5mg QQ客服:2159513211
    射干苷; Tectoridin CFN99921 611-40-5 C22H22O11 = 462.40 20mg QQ客服:3257982914
    鸢尾黄素-7-O-木糖基葡萄糖苷; Tectorigenin 7-O-xylosylglucoside CFN90784 231288-19-0 C27H30O15 = 594.5 5mg QQ客服:2056216494
    鸢尾黄素 7-O-beta-龙胆双糖苷; Tectorigenin 7-O-gentiobioside CFN95577 67604-94-8 C28H32O16 = 624.6 5mg QQ客服:2159513211
    葛花苷; Kakkalide CFN95052 58274-56-9 C28H32O15 = 608.6 10mg QQ客服:215959384
    鸢尾黄素-7-O-葡萄糖基-4'-O-葡萄糖苷; Tectorigenin-7-O-beta-glucosyl-4'-O-beta-glucoside CFN95605 848128-32-5 C28H32O16 = 624.6 10mg QQ客服:2159513211
    鸢尾甲苷A; Iristectorin A CFN95037 37744-61-9 C23H24O12 = 492.4 20mg QQ客服:2056216494
    鸢尾甲苷A-6''-O-葡萄糖苷; Iristectorin A-6''-O-glucoside CFN95597 86849-71-0 C29H34O17 = 654.6 5mg QQ客服:1413575084
    野鹫尾苷 ; Iridin CFN96557 491-74-7 C24H26O13 = 522.46 20mg QQ客服:3257982914

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