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  • N-阿魏酰真蛸胺; N- 阿魏酰章鱼胺

    N-Feruloyloctopamine

    N-阿魏酰真蛸胺; N- 阿魏酰章鱼胺
    产品编号 CFN97707
    CAS编号 66648-44-0
    分子式 = 分子量 C18H19NO5 = 329.35
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The herbs of Datura arborea
    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
    N-阿魏酰真蛸胺; N- 阿魏酰章鱼胺 CFN97707 66648-44-0 1mg QQ客服:215959384
    N-阿魏酰真蛸胺; N- 阿魏酰章鱼胺 CFN97707 66648-44-0 5mg QQ客服:215959384
    N-阿魏酰真蛸胺; N- 阿魏酰章鱼胺 CFN97707 66648-44-0 10mg QQ客服:215959384
    N-阿魏酰真蛸胺; N- 阿魏酰章鱼胺 CFN97707 66648-44-0 20mg QQ客服:215959384
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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
  • Georgia Institute of Technology (USA)
  • Mahidol University (Thailand)
  • University of Virginia (USA)
  • Amity University (India)
  • Tohoku University (Japan)
  • Universiti Sains Malaysia (Malaysia)
  • Wageningen University (Netherlands)
  • Institute of Tropical Disease Universitas Airlangga (Indonesia)
  • Srinakharinwirot University (Thailand)
  • Instituto de Investigaciones Agropecuarias (Chile)
  • Sri Sai Aditya Institute of Pharmaceutical Sciences and Research (India)
  • Chinese University of Hong Kong (China)
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • University of Pretoria (South Africa)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • FASEB J.2019, 33(8):9685-9694
  • Journal of Ginseng Research2022, j.jgr.2022.09.005.
  • J Pharmaceutical and Biomedical Analysis2022, 114631.
  • Dicle Tip Dergisi2020, 47(2),423-430.
  • Inflammation.2022, 45(6):2529-2543.
  • Current Pharmaceutical Analysis2017, 13(5)
  • J Pharm Biomed Anal.2019, 164:119-127
  • Environ Toxicol.2019, 34(12):1354-1362
  • Appl Microbiol Biotechnol.2018, 102(12):5105-5120
  • Korean J of Medicinal Crop Science2018, 220-226
  • Molecules.2020, 25(18),4089.
  • JAOCS2021, 98(7):779-794.
  • Appl. Sci.2020, 10(8),2804
  • Med Sci Monit.2019, 25:9499-9508
  • J of the Korean Society of Cosmetics and Cosmetology2019, 225-231
  • Research Square2020, doi: 10.21203.
  • J.the Korean Socie. Food Sci.&Nut.2023; 52(1):26-39.
  • Neurochem Int.2018, 121:114-124
  • Front Immunol.2018, 9:2655
  • Front Pharmacol.2020, 11:566490.
  • Asian Pac J Cancer Prev.2021, 22(S1):97-106.
  • J of Dentistry & Oral Health2019, 2641-1962
  • Environ Toxicol Pharmacol.2019, 66:109-115
  • ...
  • 生物活性
    In vitro:
    Bioorg Med Chem Lett . 2017 Feb 15;27(4):989-993.
    Inhibition of invasion by N-trans-feruloyloctopamine via AKT, p38MAPK and EMT related signals in hepatocellular carcinoma cells[Pubmed: 28073674]
    Abstract N-trans-feruloyloctopamine (FO) isolated from Garlic skin was identified as the primary antioxidant constituents, however, the effect of which on HCC invasion is still unclear. Herein, the FO was synthesized and its antitumor activities were evaluated in HCC cell lines. Cellular functional analyses have revealed that the reformed FO owns strong abilities of inhibiting cell proliferation and invasion in HCC cells. Molecular data have further showed that FO could significantly decrease the phosphorylation levels of Akt and p38 MAPK. In addition, the expression of Slug was inhibited and the level of E-cadherin increased. Molecular docking analysis indicates that the H-bond and hydrophobic interactions were critical for FO and E-cadherin binding, but FO did not seem to act directly on phosphorylated Akt and p38 MAPK. We have thus concluded that reformed FO inhibits cell invasion might be directly through EMT related signals (E-cadherin) and indirectly through PI3K/Akt, p38 MAPK signaling pathways. FO might be a promising drug in HCC treatment and prognosis. Keywords: AKT; E-cadherin; Epithelial to mesenchymal transition (EMT); Hepatocellular carcinoma; MAPK; N-trans-feruloyloctopamine (FO).
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.0363 mL 15.1814 mL 30.3628 mL 60.7257 mL 75.9071 mL
    5 mM 0.6073 mL 3.0363 mL 6.0726 mL 12.1451 mL 15.1814 mL
    10 mM 0.3036 mL 1.5181 mL 3.0363 mL 6.0726 mL 7.5907 mL
    50 mM 0.0607 mL 0.3036 mL 0.6073 mL 1.2145 mL 1.5181 mL
    100 mM 0.0304 mL 0.1518 mL 0.3036 mL 0.6073 mL 0.7591 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
    金色酰胺醇苯甲酸酯; Aurantiamide benzoate CFN91929 150881-02-0 C32H30N2O4 = 506.59 5mg QQ客服:2159513211
    大麻酰胺B; Cannabisin B CFN95268 144506-17-2 C34H32N2O8 = 596.6 5mg QQ客服:2056216494
    大麻酰胺D; Cannabisin D CFN90405 144506-19-4 C36H36N2O8 = 624.69 5 mg QQ客服:1413575084
    大麻酰胺P; Cannabisin P CFN95456 2756983-19-2 C34H34N2O9 = 614.7 5mg QQ客服:2159513211
    大麻酰胺M; Cannabisin M CFN95436 1831134-13-4 C34H32N2O8 = 596.6 5mg QQ客服:215959384
    克罗酰胺; Grossamide CFN97672 80510-06-1 C36H36N2O8 = 624.69 5mg QQ客服:3257982914
    N-反式-对香豆酰酪胺; Paprazine CFN92967 36417-86-4 C17H17NO3 = 283.32 10mg QQ客服:2056216494
    N-对香豆酰真蛸胺; N-p-Coumaroyloctopamine CFN97706 66648-45-1 C17H17NO4 = 299.32 10mg QQ客服:1457312923
    Tamgermanetin; Tamgermanetin CFN92966 640235-90-1 C18H19NO4 = 313.35 5mg QQ客服:215959384
    Cis-N-阿魏酰酪胺; Cis-N-Feruloyltyramine CFN92826 80510-09-4 C18H19NO4 = 313.4 5mg QQ客服:3257982914

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