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  • 莱菔素

    Sulforaphene

    莱菔素
    产品编号 CFN80054
    CAS编号 592-95-0
    分子式 = 分子量 C6H9NOS2 = 175.27
    产品纯度 >=98%
    物理属性 Oil
    化合物类型 Alkaloids
    植物来源 The seeds of Brassica oleracea L. var. botrytis L.
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    莱菔素 CFN80054 592-95-0 1mg QQ客服:2056216494
    莱菔素 CFN80054 592-95-0 5mg QQ客服:2056216494
    莱菔素 CFN80054 592-95-0 10mg QQ客服:2056216494
    莱菔素 CFN80054 592-95-0 20mg QQ客服:2056216494
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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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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Planta Med.2018, 84(6-07):465-474
  • Nutrients.2023, 15(6):1335.
  • Oncology Letters2018, 4690-4696
  • Environ Toxicol.2019, 34(4):513-520.
  • Metabolites.2023, 13(5):625.
  • Bull. Natl. Mus. Nat. Sci.2021, 47(2),109-114.
  • J Appl Biol Chem2021, 64(3):245-251.
  • Biomol Ther (Seoul).2019, 10.4062
  • Microorganisms.2021, 9(12):2514.
  • Molecules. 2013, 18(7):7376-88
  • Pharmacognosy Journal, 2021, 13(5).
  • Food Chem.2022, 378:131975.
  • Molecules.2019, 24(12):E2286
  • Biochem Biophys Res Commun.2018, 505(1):261-266
  • Bioorg Med Chem.2020, 28(12):115553.
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  • Applied Biological Chemistry2022, 65(77).
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  • ...
  • 生物活性
    Description: Sulforaphene may be a potential anti- triple negative breast cancer natural compound and its antiproliferation effects may be mediated by tumor suppressor Egr1; it has chemotherapeutic potential, it promotes Bax/Bcl2, MAPK-dependent human gastric cancer AGS cells apoptosis and inhibits migration via EGFR, p-ERK1/2 down-regulation; it enhances radiosensitivity of hepatocellular carcinoma through suppression of the NF-κB pathway. Sulforaphene has anti-proliferative and antibacterial properties. Sulforaphene also has herbicidal activity, the ED50 of it against velvetleaf seedlings was approximately 2×10(-4) M.
    Targets: ROS | Bcl-2/Bax | Caspase | PARP | JNK | ERK | EGFR | NF-kB | Antifection
    In vitro:
    J Chem Ecol. 1993 Oct;19(10):2279-84.
    Herbicidal activity of sulforaphene from stock (Matthiola incana).[Pubmed: 24248575]

    METHODS AND RESULTS:
    A herbicidal compound was isolated from extracts ofMatthiola incana and identified as sulforaphene (4-methylsulfinyl-3-butenyl isothiocyanate).
    CONCLUSIONS:
    The ED50 of this compound against velvetleaf seedlings was approximately 2×10(-4) M. Glucoraphenin, the glucosinolate that is the natural precursor of sulforaphene, was less phytotoxic, with an ED50 of near 6×10(-3)M.
    Breast Cancer Res Treat. 2016 Jul;158(2):277-86.
    Sulforaphene inhibits triple negative breast cancer through activating tumor suppressor Egr1.[Pubmed: 27377973 ]
    Sulforaphene (SFE, 4-methylsufinyl-3-butenyl isothiocyanate) is a member of isothiocyanates, which is derived from radish seeds. It has shown that multiple isothiocyanates, such as sulforaphane, can effectively inhibit cancer cell proliferation in vitro and in vivo. However, it is still largely unknown if SFE could impact breast cancer.
    METHODS AND RESULTS:
    In this study, we investigated the anticancer effects of SFE on triple negative breast cancer (TNBC) via a series of in vitro and in vivo assays. We found that SFE can significantly inhibit cell proliferation in multiple TNBC cell lines through inducing G2/M phase arrest as well as cell apoptosis. Nude mice xenograft assays support the anti-TNBC role of SFE in vivo. Interestingly, SFE can repress expression of cyclinB1, Cdc2, and phosphorylated Cdc2, and, then, induced G2/M phase arrest of TNBC cells. To identify SFE target genes, we detected genome-wide gene expression changes through gene expression profiling and observed 27 upregulated and 18 downregulated genes in MDA-MB-453 cells treated with SFE. Among these genes, Egr1 was successfully validated as a consistently activated gene after SFE treatment in TNBC MDA-MB-453 and MDA-MB-436 cells. Egr1 overexpression inhibited proliferation of TNBC cells. However, Egr1 knockdown using siRNAs significantly promoted TNBC cell growth, indicating the tumor suppressor nature of Egr1.
    CONCLUSIONS:
    In sum, we for the first time found that SFE might be a potential anti-TNBC natural compound and its antiproliferation effects might be mediated by tumor suppressor Egr1.
    Ashs Conference. 2013.
    Characterization of Anti-proliferative and Antibacterial Properties of Sulforaphene Obtained from Radish Seeds,[Reference: WebLink]
    Many isothiocyanates (ITCs), are a mainly hydrolysis product in glucosinolates (GSLs), have been demonstrated the noteworthy overcoming impact against the survival and proliferation of cancer cells and their modulation of apoptosis and cell cycle progression by numerous molecular basis studies (Zang et al., 2006) , such as sulforaphane (SFA) isolated from broccoli seed and sprouts. By the way, Sulforaphene (SFE), is a major ITCs in radish seed, have been reported the potency of biological activity, a little bit recently. On the other hands, while much researches were known that SFA in broccoli has the excellent anticancer effects such as induction of apoptosis and detoxification enzymes in vitro and in vivo (Fahey et al., 2002), SFE in radish was hardly the biological study in spite of their similar chemical structure in comparison with SFA.
    METHODS AND RESULTS:
    In the present study, I demonstrated the broadly biological activity of SFE against cancer cells, Helicobacter pylori (H. pylori) and multi-drug resistance pathogens. In 4 cancer cells isolated from each four organisms were notably inhibited the proliferation treated with purified SFE (IC50 = 10.0–23 μg/mL). I also characterized that SFE modulated an induction of apoptosis pathway against A549 cancer cell through the proteins expressions related with apoptosis pathway. In addition, the highly bacteriocidal potency (MIC90 = 0.6–5.0 μg/mL) of SFE was exhibited against H. pylori, particularly antibiotic resistant strain (212 strain, MIC90 = 0.6 μg/mL). MRSA (Methicillin-resistant staphylococcus aureus), is known as super bacteria, also were inhibited by SFE (MIC90 = 10–20 μg/mL), whereas the MIC 90 value of MSSA (Methicillin-susceptible staphylococcus aureus) by SFE had little significant.
    CONCLUSIONS:
    These results suggested that the antibiotic potency of SFE in radish seeds would be associated with the potency in a broad range of cancer cells and antibiotic resistant pathogens.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 5.7055 mL 28.5274 mL 57.0548 mL 114.1097 mL 142.6371 mL
    5 mM 1.1411 mL 5.7055 mL 11.411 mL 22.8219 mL 28.5274 mL
    10 mM 0.5705 mL 2.8527 mL 5.7055 mL 11.411 mL 14.2637 mL
    50 mM 0.1141 mL 0.5705 mL 1.1411 mL 2.2822 mL 2.8527 mL
    100 mM 0.0571 mL 0.2853 mL 0.5705 mL 1.1411 mL 1.4264 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
    巴西苏木素; 苏枋精; Brazilin CFN98711 474-07-7 C16H14O5 = 286.3 20mg QQ客服:1413575084
    Taibaihenryiins A; Taibaihenryiins A CFN92314 398129-59-4 C22H30O7 = 406.5 5mg QQ客服:215959384
    2,3-二羟基-12-齐墩果烯-28-酸; 2,3-Dihydroxy-12-oleanen-28-oic acid CFN98310 26563-68-8 C30H48O4 = 472.7 5mg QQ客服:2159513211
    桔梗皂苷D; Platycodin D CFN98134 58479-68-8 C57H92O28 = 1225.33 20mg QQ客服:3257982914

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