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  • 伏康京碱

    Voacangine

    伏康京碱
    产品编号 CFN92252
    CAS编号 510-22-5
    分子式 = 分子量 C22H28N2O3 = 368.5
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The herbs of Ervatamia heyneana
    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
    伏康京碱 CFN92252 510-22-5 1mg QQ客服:2056216494
    伏康京碱 CFN92252 510-22-5 5mg QQ客服:2056216494
    伏康京碱 CFN92252 510-22-5 10mg QQ客服:2056216494
    伏康京碱 CFN92252 510-22-5 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
    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
  • Tokyo Woman's Christian University (Japan)
  • Universidad de Buenos Aires (Argentina)
  • Griffith University (Australia)
  • Chinese University of Hong Kong (China)
  • Medical University of South Carolina (USA)
  • Seoul National University (Korea)
  • Kyoto University (Japan)
  • Calcutta University (India)
  • Max-Planck-Insitut (Germany)
  • Complutense University of Madrid (Spain)
  • Harvard University (USA)
  • The Australian National University (Australia)
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  • Universite Libre de Bruxelles (Belgium)
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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(15):1101-1109
  • Journal of Plant Growth Regulation2022, 10705-2.
  • J. Soc. Cosmet. Sci. Korea2021, 47(1):57-63
  • Phytochem Anal.2016, 27(5):296-303
  • Neurochem Res.2021, s11064-021-03449-0
  • J Nat Prod.2019, 82(4):1002-1008
  • Cosmetics2021, 8(3),91.
  • HIV Med.2021, 22(8):690-704.
  • Int J Mol Sci.2022, 23(23):14545.
  • Aquaculture2019, 510:392-399
  • Pharmaceuticals (Basel).2021, 14(6):588.
  • Molecules.2023, 28(8):3414.
  • Cell.2018, 172(1-2):249-261
  • Neurotox Res.2020, 38(1):163-174.
  • Plants (Basel).2021, 10(4):702.
  • Plant J.2021, 107(6):1711-1723.
  • Plant Physiol Biochem.2023, 203:108073.
  • J Insect Sci.2020, 20(5):18.
  • Phytother Res.2023, 37(10):4587-4606.
  • Adaptive Medicine 2020, 12(1): 4-10
  • Theoretical and Experimental Plant Physiology 2022, 34,53-62
  • Asian J Beauty Cosmetol2016, 14(3):249-257
  • Front Nutr.2021, 8: 687851.
  • ...
  • 生物活性
    Description: Voacangine is a novel transient receptor potential vanilloid type 1 (TRPV1) antagonist, it shows mod. cytotoxic activity, also some CNS, brachycardial and hypotensive action.Voacangine significantly suppresses in vitro angiogenesis, such as VEGF-induced tube formation and chemoinvasion.
    Targets: TRPV | VEGFR
    In vitro:
    Biochem Biophys Res Commun. 2012 Jan 6;417(1):330-4.
    A natural small molecule voacangine inhibits angiogenesis both in vitro and in vivo.[Pubmed: 22155252]
    Angiogenesis, the formation of new blood vessels from pre-existing ones, plays a critical role in normal and pathological phenotypes, including solid tumor growth and metastasis. Accordingly, the development of new anti-angiogenic agents is considered an efficient strategy for the treatment of cancer and other human diseases linked with angiogenesis.
    METHODS AND RESULTS:
    We have identified Voacangine, isolated from Voacanga africana, as a novel anti-angiogenic agent. Voacangine inhibits the proliferation of HUVECs at an IC(50) of 18 μM with no cytotoxic effects. Voacangine significantly suppressed in vitro angiogenesis, such as VEGF-induced tube formation and chemoinvasion. Moreover, the compound inhibits in vivo angiogenesis in the chorioallantoic membrane at non-toxic doses. In addition, Voacangine decreased the expression levels of hypoxia inducible factor-1α and its target gene, VEGF, in a dose-dependent manner.
    CONCLUSIONS:
    Taken together, these results suggest that the naturally occurring compound, Voacangine, is a novel anti-angiogenic compound.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.7137 mL 13.5685 mL 27.137 mL 54.2741 mL 67.8426 mL
    5 mM 0.5427 mL 2.7137 mL 5.4274 mL 10.8548 mL 13.5685 mL
    10 mM 0.2714 mL 1.3569 mL 2.7137 mL 5.4274 mL 6.7843 mL
    50 mM 0.0543 mL 0.2714 mL 0.5427 mL 1.0855 mL 1.3569 mL
    100 mM 0.0271 mL 0.1357 mL 0.2714 mL 0.5427 mL 0.6784 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
    Crassanine; Crassanine CFN96176 16790-92-4 C23H30N2O5 = 414.5 5mg QQ客服:1413575084
    长春质碱; Catharanthine CFN99765 2468-21-5 C21H24N2O2 = 336.43 20mg QQ客服:1413575084
    酒石酸长春质碱; Catharanthine Tartrate CFN90318 2648-21-5 C21H24N2O2.C4H6O6 = 486.40 20mg QQ客服:1457312923
    硫酸长春质碱; Catharanthine Sulfate CFN93298 70674-90-7 C21H26N2O6S = 434.51 5mg QQ客服:215959384
    19,20-(E)-瓦来萨明碱; 19,20-(E)-Vallesamine CFN98432 3368-87-4 C20H24N2O3 = 340.4 5mg QQ客服:1413575084
    瓦来萨明碱 N-氧化物; Vallesamine N-oxide CFN99377 126594-73-8 C20H24N2O4 = 356.4 5mg QQ客服:1457312923
    去甲氧羰基蕊木碱甲酯; Methyl demethoxycarbonylchanofruticosinate CFN97275 80151-89-9 C21H24N2O3 = 352.4 5mg QQ客服:1457312923
    11,12-De(methylenedioxy)danuphylline; 11,12-De(methylenedioxy)danuphylline CFN97456 888482-17-5 C23H26N2O6 = 426.5 5mg QQ客服:2159513211
    蕊木碱甲酯; Methyl chanofruticosinate CFN99459 14050-92-1 C23H26N2O5 = 410.5 5mg QQ客服:1457312923
    白坚木辛碱; Apparicine CFN96107 2122-36-3 C18H20N2 = 264.4 5mg QQ客服:1457312923

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