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  • 达卡他韦

    Daclatasvir (BMS-790052)

    达卡他韦
    产品编号 CFN60069
    CAS编号 1009119-64-5
    分子式 = 分子量 C40H50N8O6 = 738.88
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源
    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
    达卡他韦 CFN60069 1009119-64-5 1mg QQ客服:3257982914
    达卡他韦 CFN60069 1009119-64-5 5mg QQ客服:3257982914
    达卡他韦 CFN60069 1009119-64-5 10mg QQ客服:3257982914
    达卡他韦 CFN60069 1009119-64-5 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.
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    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
  • Kyushu University (Japan)
  • Universidad Industrial de Santander (Colombia)
  • Anna University (India)
  • Universidade Federal de Goias (UFG) (Brazil)
  • Subang Jaya Medical Centre (Malaysia)
  • Universidade da Beira Interior (Germany)
  • Seoul National University of Science and Technology (Korea)
  • Institute of Tropical Disease Universitas Airlangga (Indonesia)
  • Osmania University (India)
  • Aarhus University (Denmark)
  • Sant Gadge Baba Amravati University (India)
  • University of Liège (Belgium)
  • Centrum Menselijke Erfelijkheid (Belgium)
  • University of East Anglia (United Kingdom)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Int J Med Sci.2021, 18(10):2155-2161.
  • Int J Mol Sci.2019, 20(21):E5488
  • Molecules.2019, 24(24):E4536
  • Molecules.2019, 24(11):E2044
  • Exp Parasitol.2018, 194:67-78
  • J Pharmaceut Biomed2020, 178:112894
  • Toxicol In Vitro.2022, 81:105346.
  • Integr Med Res.2021, 10(3):100723.
  • Antioxidants (Basel).2021, 10(11): 1802.
  • Korean J of Crop Science2019, 452-458
  • Biochem Biophys Res Commun.2020, 522(1):40-46
  • Chemistry of Natural Compounds2018, 54(3):572-576
  • J Ethnopharmacol.2020, 269:113752.
  • J Agric Food Chem.2019, 67(27):7748-7754
  • Asian Journal of Chemistry2014, 26(8):2425
  • J Pharmaceut Biomed2020, 182:113110
  • Food Res Int.2021, 148:110607.
  • Pharmacognosy Journal2019, 11,6:1235-1241
  • Int J Mol Sci.2019, 20(3):E651
  • HortTechnology2016, 26(6):816-819
  • Front Pharmacol.2017, 8:673
  • Food and Fermentation Industries2018, 44(371)
  • Int J Mol Sci.2022, 23(5):2796.
  • ...
  • 生物活性
    Description: Daclatasvir (BMS-790052, EBP883) is a highly selective inhibitor of HCV NS5A with EC50 of 9-50 pM, for a broad range of HCV replicon genotypes and the JFH-1 genotype 2a infectious virus in cell culture.
    Targets: HCV NS5A
    In vitro:
    Virology,2011 May 25;414(1):10-8.
    The hepatitis C virus NS5A inhibitor (BMS-790052) alters the subcellular localization of the NS5A non-structural viral protein.[Pubmed: 21513964]
    The hepatitis C virus (HCV) non-structural (NS) 5A protein plays an essential role in the replication of the viral RNA by the membrane-associated replication complex (RC). Recently, a putative NS5A inhibitor, BMS-790052, exhibited the highest potency of any known anti-HCV compound in inhibiting HCV replication in vitro and showed a promising clinical effect in HCV-infected patients. The precise mechanism of action for this new class of potential anti-HCV therapeutics, however, is still unclear.
    METHODS AND RESULTS:
    In order to gain further insight into its mode of action, we sought to test the hypothesis that the antiviral effect of BMS-790052 might be mediated by interfering with the functional assembly of the HCV RC. We observed that BMS-790052 indeed altered the subcellular localization and biochemical fractionation of NS5A.
    CONCLUSIONS:
    Taken together, our data suggest that NS5A inhibitors such as BMS-790052 can suppress viral genome replication by altering the proper localization of NS5A into functional RCs.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.3534 mL 6.767 mL 13.534 mL 27.068 mL 33.835 mL
    5 mM 0.2707 mL 1.3534 mL 2.7068 mL 5.4136 mL 6.767 mL
    10 mM 0.1353 mL 0.6767 mL 1.3534 mL 2.7068 mL 3.3835 mL
    50 mM 0.0271 mL 0.1353 mL 0.2707 mL 0.5414 mL 0.6767 mL
    100 mM 0.0135 mL 0.0677 mL 0.1353 mL 0.2707 mL 0.3383 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
    苦瓜素 I; Momordicine I CFN92076 91590-76-0 C30H48O4 = 472.7 10mg QQ客服:3257982914
    买麻藤素D; Gnetin D CFN92423 84870-53-1 C28H22O7 = 470.5 5mg QQ客服:2159513211
    鸦胆子素C; Bruceine C CFN91974 25514-30-1 C28H36O12 = 564.58 5mg QQ客服:3257982914
    Neotripterifordin; Neotripterifordin CFN89189 149249-32-1 C20H30O3 = 318.45 5mg QQ客服:1413575084

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