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  • 脱氧鸭嘴花碱酮

    Deoxyvasicinone

    脱氧鸭嘴花碱酮
    产品编号 CFN98882
    CAS编号 530-53-0
    分子式 = 分子量 C11H10N2O = 186.2
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The herbs of Galium aparine 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
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    脱氧鸭嘴花碱酮 CFN98882 530-53-0 1mg QQ客服:3257982914
    脱氧鸭嘴花碱酮 CFN98882 530-53-0 5mg QQ客服:3257982914
    脱氧鸭嘴花碱酮 CFN98882 530-53-0 10mg QQ客服:3257982914
    脱氧鸭嘴花碱酮 CFN98882 530-53-0 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
  • The Australian National University (Australia)
  • Helmholtz Zentrum München (Germany)
  • Donald Danforth Plant Science Center (USA)
  • Universidade do Porto (Portugal)
  • University of Beira Interior (Portugal)
  • Yale University (USA)
  • Calcutta University (India)
  • Universidade Federal de Goias (UFG) (Brazil)
  • Charles Sturt University (Denmark)
  • Instituto de Investigaciones Agropecuarias (Chile)
  • Universit?t Basel (Switzerland)
  • Rio de Janeiro State University (Brazil)
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • University of Melbourne (Australia)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Chemistry of Plant Raw Materials2022, 20220210569.
  • Int J Mol Sci.2022, 23(13):7115.
  • Antioxidants (Basel).2020, 9(6):544.
  • Mol Cells.2015, 38(9):765-72
  • Acta Physiologiae Plantarum2016, 38:7
  • Ind Crops Prod.2015, 67:185-191
  • Chin J Appl. Physiol.2019, 35(3):283-288
  • JPC-Journal of Planar Chromatography 2017, 30(4)
  • Environ Toxicol.2021, 36(9):1848-1856.
  • J of Health Science and Alternative Medicine2019, 1(1)
  • FASEB J.2019, 33(2):2026-2036
  • Research Square2023, 2883170.
  • Mol Biol Rep.2022, doi: 10.1007
  • Asian Pac J Cancer Prev.2021, 22(S1):97-106.
  • Planta Med.2018, 84(15):1101-1109
  • Front Microbiol.2019, 10:2806
  • J Pharm Biomed Anal.2021, 196:113931.
  • Biomed Pharmacother.2021, 139:111585.
  • Front Nutr.2021, 8: 687851.
  • Korean Journal of Pharmacognosy2014, 113-120
  • J Tradit Chin Med.2023, 43(6):1081-1091.
  • Biochem Biophys Res Commun.2019, 518(4):732-738
  • Pamukkale Medical Journal2022, 15(4):796-803.
  • ...
  • 生物活性
    Description: Deoxyvasicinone derivatives can be considered as promising lead molecules for the development of more potent inhibitors of NEDD8-activating enzyme.
    In vitro:
    Methods. 2015 Jan;71:71-6.
    Discovery of deoxyvasicinone derivatives as inhibitors of NEDD8-activating enzyme.[Pubmed: 25196325]
    NEDD8-activating enzyme (NAE) controls the specific degradation of proteins regulated by cullin-RING ubiquitin E3 ligases, and has been considered as an attractive molecular target for the development of drugs against cancer.
    METHODS AND RESULTS:
    A pharmacophore model constructed from a training set of Deoxyvasicinone derivatives was used to screen 376 compounds from an analogue database. From the initial screening, the valine-linked Deoxyvasicinone derivative 9 and the N-isopropyl-linked Deoxyvasicinone derivative 10 emerged as the top scoring candidates. Compounds 9 and 10 showed micromolar potencies in both cell-free and cell-based systems, with selectivity for NAE over the related enzymes SAE and UAE. Molecular modelling analysis suggested that 9 and 10 may inhibit NAE by blocking the ATP-binding domain.
    CONCLUSIONS:
    Thus, these Deoxyvasicinone derivatives could be considered as promising lead molecules for the development of more potent inhibitors of NAE.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 5.3706 mL 26.8528 mL 53.7057 mL 107.4114 mL 134.2642 mL
    5 mM 1.0741 mL 5.3706 mL 10.7411 mL 21.4823 mL 26.8528 mL
    10 mM 0.5371 mL 2.6853 mL 5.3706 mL 10.7411 mL 13.4264 mL
    50 mM 0.1074 mL 0.5371 mL 1.0741 mL 2.1482 mL 2.6853 mL
    100 mM 0.0537 mL 0.2685 mL 0.5371 mL 1.0741 mL 1.3426 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
    常山乙素; Febrifugine CFN92302 24159-07-7 C16H19N3O3 = 301.3 20mg QQ客服:3257982914
    异常山乙素; Isofebrifugine CFN92303 32434-44-9 C16H19N3O3 = 301.3 20mg QQ客服:2159513211
    Desoxypeganine; Desoxypeganine CFN91939 495-59-0 C11H12N2 = 172.23 5mg QQ客服:1457312923
    骆驼蓬碱; Vasicine CFN97052 6159-55-3 C11H12N2O = 188.2 10mg QQ客服:1457312923
    鸭嘴花酚碱; Vasicinol CFN99009 5081-51-6 C11H12N2O2 = 204.2 5mg QQ客服:2056216494
    脱氧鸭嘴花碱酮; Deoxyvasicinone CFN98882 530-53-0 C11H10N2O = 186.2 5mg QQ客服:1457312923
    鸭嘴花碱酮; Vasicinone CFN98773 486-64-6 C11H10N2O2 = 202.2 5mg QQ客服:2056216494
    鸭嘴花碱酮; Vasicinolone CFN97406 84847-50-7 C11H10N2O3 = 218.2 5mg QQ客服:215959384
    薏苡素; Coixol CFN98889 532-91-2 C8H7NO3 = 165.1 20mg QQ客服:2056216494
    2,7-二羟基-2H-1,4-苯并嗪-3(4H)-酮; 2,7-Dihydroxy-2H-1,4-benzoxazin-3(4H)-one CFN97184 69804-59-7 C8H7NO4 = 181.1 5mg QQ客服:3257982914

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