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  • 槐黄烷酮G

    Sophoraflavanone G

    槐黄烷酮G
    产品编号 CFN92005
    CAS编号 97938-30-2
    分子式 = 分子量 C25H28O6 = 424.5
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Flavonoids
    植物来源 The roots of Sophora flavescens Ait.
    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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    产品名称 产品编号 CAS编号 包装 QQ客服
    槐黄烷酮G CFN92005 97938-30-2 10mg QQ客服:1457312923
    槐黄烷酮G CFN92005 97938-30-2 20mg QQ客服:1457312923
    槐黄烷酮G CFN92005 97938-30-2 50mg QQ客服:1457312923
    槐黄烷酮G CFN92005 97938-30-2 100mg 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
  • University of Otago (New Zealand)
  • Chang Gung University (Taiwan)
  • University of Wuerzburg (Germany)
  • Helmholtz Zentrum München (Germany)
  • Stanford University (USA)
  • Max-Planck-Insitut (Germany)
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • FORTH-IMBB (Greece)
  • Indian Institute of Science (India)
  • Leibniz Institute of Plant Biochemistry (Germany)
  • Center for protein Engineering (CIP) (Belgium)
  • Worcester Polytechnic Institute (USA)
  • The Australian National University (Australia)
  • University of Limpopo (South Africa)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Toxicol Appl Pharmacol.2022, 434:115815.
  • Advances in Traditional Medicine 2021, 21:779-789.
  • J of the Korean Society of Cosmetics and Cosmetology2019, 225-231
  • Int J Mol Sci.2022, 23(23):14826.
  • Biomed Pharmacother.2024, 176:116765.
  • Processes2023, 11(2), 385。
  • Inflammation.2020, 43(5):1716-1728.
  • Int J Mol Sci.2017, 19(1)
  • J Mater Chem B.2019, 7(39):5896-5919
  • Microchemical Journal2022, 182: 107874.
  • Environ Toxicol.2019, 34(12):1354-1362
  • Cell Prolif.2021, 54(8):e13083.
  • J Med Food.2020, 23(6):633-640.
  • Molecules.2023, 28(13):4907.
  • JEJU National University2022, 10478.
  • Journal of Ginseng Research2021, 3 June.
  • Int J Mol Sci.2023, 24(17):13230.
  • Int J Immunopathol Pharmacol.2019, 33:2058738419857537
  • PLoS One.2017, 12(3):e0173585
  • Int J Mol Sci.2024, 25(5):2799.
  • Academic J of Second Military Medical University2019, 40(1)
  • Heliyon.2024, 10(7):e28755.
  • ACS Synth Biol.2022, 11(10):3296-3304.
  • ...
  • 生物活性
    Description: Sophoraflavanone G has an anti-inflammatory effect, it has strong antimicrobial activity against mutans streptococci and could be useful in the development of novel oral hygiene products, such as a gargle solution or dentifrice. Sophoraflavanone G is a novel small-molecule inhibitor, it inhibits the NF-κB and MAPK signaling pathways.
    Targets: STAT | JAK | Akt | ERK | NF-kB | P450 (e.g. CYP17) | Antifection | COX | NOS | PGE | HO-1 | TNF-α | MAPK | p65
    In vitro:
    Anaerobe. 2013 Feb;19:17-21.
    Antimicrobial effect of sophoraflavanone G isolated from Sophora flavescens against mutans streptococci.[Pubmed: 23178373]

    METHODS AND RESULTS:
    In this study, the antibacterial properties of sophoraflavanone G isolated from the methanol extract of Sophora flavescens were tested against 16 strains of mutans streptococci to screen and determine the optimal concentration of anti-caries natural extract. The antimicrobial activity was evaluated by measuring minimum bactericidal concentration (MBC). The cell viability of normal human gingival fibroblast (NHGF) cells was tested using the methyl thiazolyl tetrazolium assay after exposure to sophoraflavanone G. The data showed that sophoraflavanone G had a remarkable antimicrobial effect on the bacteria tested with an MBC ranging from 0.5 μg/ml to 4 μg/ml. Sophoraflavanone G had no cytotoxic effect on NHGF cells at concentrations where it produced an antimicrobial effect.
    CONCLUSIONS:
    These findings demonstrate that sophoraflavanone G has strong antimicrobial activity against mutans streptococci and could be useful in the development of novel oral hygiene products, such as a gargle solution or dentifrice.
    Phytother Res. 2009 Sep;23(9):1326-31.
    Antibacterial activity of sophoraflavanone G isolated from the roots of Sophora flavescens against methicillin-resistant Staphylococcus aureus.[Pubmed: 19288534]

    METHODS AND RESULTS:
    In this study, sophoraflavanone G obtained from Sophora flavescens was evaluated against 10 clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA), either alone or in combination with ampicillin or oxacillin, via checkerboard assay. At the end point of an optically clear well, the minimum inhibitory concentrations (MICs) ranged from 0.5 to 8 microg/ml for sophoraflavanone G, from 64 to 1024 microg/ml for ampicillin, and from 256 to 1024 microg/ml for oxacillin. The combination of sophoraflavanone G and ampicillin or oxacillin yielded a fractional inhibitory concentration index ranging from 0.188 to 0.375, thereby indicating a principally synergistic effect. The synergistic interaction was verified by time-kill studies using sophoraflavanone G and/or antibiotics. Thirty minutes of treatment with sophoraflavanone G with ampicillin or oxacillin resulted in an increase in the rate of killing in units of CFU/ml to a greater degree than was observed with Sophoraflavanone G alone.
    CONCLUSIONS:
    These findings indicated that the application of the tested sophoraflavanone G alone or in combination with antibiotics might prove useful in the control and treatment of MRSA infections.
    Am J Chin Med . 2016;44(1):165-76.
    Sophoraflavanone G Induces Apoptosis in Human Leukemia Cells and Blocks MAPK Activation[Pubmed: 26916921]
    Abstract Sophoraflavanone G (SG) was isolated from Sophora flavescens. Previously, we have found that SG is able to suppress the inflammatory response in lipopolysaccharide-stimulated RAW 264.7 macrophages. This study aimed to evaluate the effects of SG on apoptosis, and explore its molecular mechanism in human leukemia HL-60 cells. HL-60 cells were treated with various concentrations of SG (3-30 [Formula: see text]M). The viability of the HL-60 cells was assessed using the MTT method, and the nuclear condensation indicative of apoptosis was observed by DAPI fluorescence staining. In addition, apoptotic signal proteins were examined using Western blotting. The results showed that apoptosis, including DNA fragmentation and nuclear condensation, increased significantly in SG-treated HL-60 cells. SG activated caspase-3 and caspase-9, and downregulated Bcl-2 and Bcl-xL. SG also upregulated Bax and released cytochrome c from the mitochondria into the cytoplasm, enabling apoptosis via the mitochondrially-mediated "intrinsic" pathway. Additionally, SG was able to cleave poly (ADP-ribose) polymerase 1 and activate mitogen-activated protein kinase (MAPK) pathways. These results suggest that SG might increase the effect of apoptosis on HL-60 cells through caspase-3 activation, mitochondrial-mediated pathways, and the MAPK pathway.
    Phytomedicine . 2019 Aug;61:152852.
    Sophoraflavanone G from Sophora flavescens induces apoptosis in triple-negative breast cancer cells[Pubmed: 31035052]
    Abstract Background: A compound isolated from Sophora flavescens-sophoraflavanone G (SG)-showed anti-tumor and anti-inflammatory properties. We previously demonstrated that SG promoted apoptosis in human leukemia HL-60 cells. In the present study, we investigated the effects of SG on apoptosis in human breast cancer MDA-MB-231 cells, and explored the underlying molecular mechanisms. Methods: MDA-MB-231 cells were treated with various SG concentrations, and cell viability was evaluated by MTT assay. Apoptotic signal proteins were detected by western blotting, and cell apoptosis was assessed using flow cytometry. Results: Our results demonstrated that SG induced nuclear condensation, DNA fragmentation, reactive oxygen species production, and increased cell apoptosis in MDA-MB-231 cells. SG also suppressed migration and invasion, likely via blockage of the MAPK pathway. In the apoptotic signaling pathway, SG increased cleaved caspase-8, caspase-3, and caspase-9. SG treatment also decreased Bcl-2 and Bcl-xL expression, increased Bax expression, and prompted release of more cytochrome c from mitochondria to the cytoplasm in MDA-MB-231 cells. Conclusion: Overall, our findings suggest that SG might increase apoptosis, and decrease migration and invasion, in MDA-MB-231 cells through suppression of a MAPK-related pathway. Keywords: Apoptosis; Caspase-3; MDA-MB-231 cells; Sophoraflavanone G.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3557 mL 11.7786 mL 23.5571 mL 47.1143 mL 58.8928 mL
    5 mM 0.4711 mL 2.3557 mL 4.7114 mL 9.4229 mL 11.7786 mL
    10 mM 0.2356 mL 1.1779 mL 2.3557 mL 4.7114 mL 5.8893 mL
    50 mM 0.0471 mL 0.2356 mL 0.4711 mL 0.9423 mL 1.1779 mL
    100 mM 0.0236 mL 0.1178 mL 0.2356 mL 0.4711 mL 0.5889 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
    槐黄烷酮G; Sophoraflavanone G CFN92005 97938-30-2 C25H28O6 = 424.5 20mg QQ客服:3257982914
    苦参新醇 F; Kushenol F CFN93051 34981-24-3 C25H28O6 = 424.5 5mg QQ客服:215959384
    苦参黄素,苦参酮; Kurarinone CFN92003 34981-26-5 C26H30O6 = 438.5 20mg QQ客服:1413575084
    苦参醇; Kurarinol CFN92533 855746-98-4 C26H32O7 = 456.5 5mg QQ客服:215959384
    里查酮A; Leachianone A CFN97560 97938-31-3 C26H30O6 = 438.5 5mg QQ客服:3257982914
    2'-甲氧基苦参黄素; 2'-Methoxykurarinone CFN92004 270249-38-2 C27H32O6 = 452.6 5mg QQ客服:2056216494
    苦参醇B; Kushenol B CFN92348 99217-64-8 C30H36O6 = 492.6 5mg QQ客服:1457312923
    槐黄烷酮 I; Sophoraflavanone I CFN96552 136997-69-8 C39H38O9 = 650.72 5mg QQ客服:1457312923
    槐黄烷酮 H; Sophoraflavanone H CFN96553 136997-68-7 C34H30O9 = 582.60 5mg QQ客服:3257982914
    Alopecurone A; Alopecurone A CFN95512 162558-89-6 C39H38O9 = 650.7 10mg QQ客服:2056216494

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