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  • 中药标准品生产商,产品定制服务
  • 羟基洋地黄毒苷

    Gitoxin

    羟基洋地黄毒苷
    产品编号 CFN70364
    CAS编号 4562-36-1
    分子式 = 分子量 C41H64O14 = 781.0
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Steroids
    植物来源 The herbs of Digitalis lanata
    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
    羟基洋地黄毒苷 CFN70364 4562-36-1 1mg QQ客服:3257982914
    羟基洋地黄毒苷 CFN70364 4562-36-1 5mg QQ客服:3257982914
    羟基洋地黄毒苷 CFN70364 4562-36-1 10mg QQ客服:3257982914
    羟基洋地黄毒苷 CFN70364 4562-36-1 20mg QQ客服:3257982914
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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
  • Mahidol University (Thailand)
  • University of Wisconsin-Madison (USA)
  • Charles Sturt University (Denmark)
  • Instituto Politécnico de Bragan?a (Portugal)
  • Aveiro University (Portugal)
  • Copenhagen University (Denmark)
  • University of Vigo (Spain)
  • University of Hull (United Kingdom)
  • Leibniz-Institut für Pflanzenbiochemie (IPB) (Germany)
  • Vin?a Institute of Nuclear Sciences (Serbia)
  • Helmholtz Zentrum München (Germany)
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • Aarhus University (Denmark)
  • Wageningen University (Netherlands)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • JEJU National University2022, 10478.
  • Evid Based Complement Alternat Med.2021, 2021:6687513.
  • Front Plant Sci.2018, 9:1424
  • Acta Pharmaceutica Hungarica2016, 86:35-40
  • Life (Basel).2021, 11(12):1399.
  • Histol Histopathol.2022, 18518.
  • Mol Med Rep.2023 Oct;28(4):193.
  • BMB Rep.2020, 53(4):218-222.
  • Molecules.2018, 23(7):E1817
  • Rev. Chim.2020, 71(3),558-564
  • Drug Des Devel Ther.2020, 14:5189-5204.
  • J Microbiol Immunol Infect.2021, S1684-1182(21)00142-0.
  • Inflammation.2020, 43(5):1716-1728.
  • Biomol Ther (Seoul).2020, 28(6):542-548.
  • Phytomedicine.2015, 22(14):1262-8
  • Pharm Biol.2021, 59(1):134-145.
  • Environ Toxicol Pharmacol.2019, 66:109-115
  • Molecules.2022, 27(7):2093.
  • Phys Chem Chem Phys.2018, 20(23):15986-15994
  • Sci Adv.2018, 4(10)
  • Int. J. Mol. Sci. 2022, 23(3),1696.
  • Planta Med.2019, 85(3):217-224
  • PLoS One.2015, 10(5):e0127060
  • ...
  • 生物活性
    Description: Gitoxin may offer a potential treatment for drug resistant NSCLC.It inhibited the phosphorylation of Erk1/2 in a dosage and time dependent way.
    Targets: ERK
    In vitro:
    Basic & Clinical Medicine, 2013.
    Inhibitory effect of gitoxin on non-small cell lung cancer with gefitinib resistance.[Reference: WebLink]
    To evaluate the inhibitory effect of gitoxin on non small cell lung cancer with drug-resistance in vitro and in vivo and to explore the underlying molecular mechanism.
    METHODS AND RESULTS:
    Survival and apoptosis rates of H1975 were measured by MTS assay and flow cytometry respectively after gitoxin and gefitinib treatments.Tumor volumes of gitoxin treated xenograft nude mice were calculated by measuring the lengths and widths of these tumors.The phosphorylation of Erk1/2 was analyzed by Western blot. Gitoxin inhibited the growth of H1975 and induced its apoptosis more effectively than gefitinib.It also inhibited growth of transplanted tumors in nude mice.In addition,gitoxin inhibited the phosphorylation of Erk1/2 in a dosage and time dependent way.
    CONCLUSIONS:
    Gitoxin may offer a potential treatment for drug resistant NSCLC.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.2804 mL 6.402 mL 12.8041 mL 25.6082 mL 32.0102 mL
    5 mM 0.2561 mL 1.2804 mL 2.5608 mL 5.1216 mL 6.402 mL
    10 mM 0.128 mL 0.6402 mL 1.2804 mL 2.5608 mL 3.201 mL
    50 mM 0.0256 mL 0.128 mL 0.2561 mL 0.5122 mL 0.6402 mL
    100 mM 0.0128 mL 0.064 mL 0.128 mL 0.2561 mL 0.3201 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
    Stauntosaponin A; Stauntosaponin A CFN96658 1417887-91-2 C28H38O7 = 486.60 5mg QQ客服:2056216494
    蔓茎毒毛旋花子苷; Sarmentocymarin CFN89202 98633-61-5 C30H46O8 = 534.69 5mg QQ客服:1457312923
    Cryptanoside A; Cryptanoside A CFN89193 98570-81-1 C30H42O10 = 562.65 5mg QQ客服:2056216494
    黄夹次甙乙; 17alpha-Neriifolin CFN97195 7044-31-7 C30H46O8 = 534.7 5mg QQ客服:1457312923
    奥多诺甙H; Odoroside H CFN99868 18810-25-8 C30H46O8 = 534.7 5mg QQ客服:2056216494
    乌沙苷元洋地黄苷; Uzarigenin digitaloside CFN97718 61217-80-9 C30H46O8 = 534.69 5mg QQ客服:3257982914
    夹竹桃它罗苷 ; Neritaloside CFN98691 465-13-4 C32H48O10 = 592.7 5mg QQ客服:1413575084
    欧夹竹桃苷; Oleandrin CFN98693 465-16-7 C32H48O9 = 576.7 20mg QQ客服:2056216494
    黄夹竹桃乙糖苷; Thevebioside CFN99245 114586-47-9 C36H56O13 = 696.8 5mg QQ客服:3257982914
    17alpha-黄夹竹桃乙糖苷; 17alpha-Thevebioside CFN99246 114613-59-1 C36H56O13 = 696.8 5mg QQ客服:2159513211

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