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  • 竹节香附素A

    Raddeanin A

    竹节香附素A
    产品编号 CFN99985
    CAS编号 89412-79-3
    分子式 = 分子量 C47H76O16 = 897.11
    产品纯度 >=98%
    物理属性 White powder
    化合物类型 Triterpenoids
    植物来源 The roots of Anemone raddeana Regel
    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
    竹节香附素A CFN99985 89412-79-3 10mg QQ客服:1413575084
    竹节香附素A CFN99985 89412-79-3 20mg QQ客服:1413575084
    竹节香附素A CFN99985 89412-79-3 50mg QQ客服:1413575084
    竹节香附素A CFN99985 89412-79-3 100mg QQ客服:1413575084
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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
  • University of Hawaii Cancer Center (USA)
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  • Universidad Industrial de Santander (Colombia)
  • Washington State University (USA)
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  • Charles Sturt University (Denmark)
  • Sri Sai Aditya Institute of Pharmaceutical Sciences and Research (India)
  • Universidad de Antioquia (Colombia)
  • John Innes Centre (United Kingdom)
  • University of Vienna (Austria)
  • Universiti Sains Malaysia (Malaysia)
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  • Vin?a Institute of Nuclear Sciences (Serbia)
  • Tohoku University (Japan)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Nutrients.2019, 11(4):E936
  • Foods.2022, 11(6):882.
  • Korea Institute of Oriental Medicine2020, doi: 10.21203.
  • Journal of Functional Foods2022, 91:105019.
  • Molecules.2020, 25(20):4851.
  • Crystals2020, 10(3), 206.
  • Horticulturae2022, 8(10), 975.
  • J Nutr Biochem.2022, 107:109064.
  • Journal of Functional Foods2017, 30:30-38
  • Auburn University2015, 1-58
  • Neurotoxicology.2022, 91:218-227.
  • Hortic Res.2023, 10(9):uhad154.
  • Korean J Environ Agric.2018, 37(4):260-267
  • Bioorg Med Chem.2020, 28(12):115553.
  • Front Plant Sci.2020, 10:1705
  • International J of Green Pharmacy2019, 13(3)
  • Neurochem Int.2023, 167:105537.
  • Pharm Biol.2016, 54(7):1255-62
  • Res Rep Urol.2022, 14:313-326.
  • Mol Neurobiol.2023, 60(12):7196-7207.
  • Applied Biological Chemistry 2022, 65,5(2022).
  • Phytomedicine.2021, 83:153483.
  • Food Res Int.2022, 157:111397.
  • ...
  • 生物活性
    Description: Raddeanin A, a histone deacetylases (HDACs) inhibitor, has high antiangiogenic potency, and antitumor activity, it can suppress the growth of liver and cells, it also inhibits proliferation of GC cells (BGC-823, SGC-7901 and MKN-28), induces their and inhibits the abilities of invasion, migration.
    Targets: VEGFR | JAK | FAK | Src | Akt | HDAC | Bcl-2/Bax | Caspase | PARP | MMP(e.g.TIMP)
    In vitro:
    Phytomedicine. 2015 Jan 15;22(1):103-10.
    Raddeanin A, a triterpenoid saponin isolated from Anemone raddeana, suppresses the angiogenesis and growth of human colorectal tumor by inhibiting VEGFR2 signaling.[Pubmed: 25636878]
    Raddeanin A (RA) is an active triterpenoid saponin from a traditional Chinese medicinal herb, Anemone raddeana Regel. It was previously reported that RA possessed attractive antitumor activity through inhibiting proliferation and inducing apoptosis of multiple cancer cells. However, whether RA can inhibit angiogenesis, an essential step in cancer development, remains unknown.
    METHODS AND RESULTS:
    In this study, we found that RA could significantly inhibit human umbilical vein endothelial cell (HUVEC) proliferation, motility, migration, and tube formation. RA also dramatically reduced angiogenesis in chick embryo chorioallantoic membrane (CAM), restrained the trunk angiogenesis in zebrafish, and suppressed angiogenesis and growth of human HCT-15 colorectal cancer xenograft in mice. Western blot assay showed that RA suppressed VEGF-induced phosphorylation of VEGFR2 and its downstream protein kinases including PLCγ1, JAK2, FAK, Src, and Akt. Molecular docking simulation indicated that RA formed hydrogen bonds and hydrophobic interactions within the ATP binding pocket of VEGFR2 kinase domain.
    CONCLUSIONS:
    Our study firstly provides the evidence that RA has high antiangiogenic potency and explores its molecular basis, demonstrating that RA is a potential agent or lead candidate for antiangiogenic cancer therapy.
    Biochem Biophys Res Commun. 2013 Sep 20;439(2):196-202.
    Raddeanin A induces human gastric cancer cells apoptosis and inhibits their invasion in vitro.[Pubmed: 23988447]
    Raddeanin A is one of the triterpenoid saponins in herbal medicine Anemone raddeana Regel which was reported to suppress the growth of liver and lung cancer cells. However, little was known about its effect on gastric cancer (GC) cells. This study aimed to investigate its inhibitory effect on three kinds of different differentiation stage GC cells (BGC-823, SGC-7901 and MKN-28) in vitro and the possible mechanisms.
    METHODS AND RESULTS:
    Proliferation assay and flow cytometry demonstrated Raddeanin A's dose-dependent inhibitory effect and determined its induction of cells apoptosis, respectively. Transwell assay, wounding heal assay and cell matrix adhesion assay showed that Raddeanin A significantly inhibited the abilities of the invasion, migration and adhesion of the BGC-823 cells. Moreover, quantitative real time PCR and Western blot analysis found that Raddeanin A increased Bax expression while reduced Bcl-2, Bcl-xL and Survivin expressions and significantly activated caspase-3, caspase-8, caspase-9 and poly-ADP ribose polymerase (PARP). Besides, Raddeanin A could also up-regulate the expression of reversion inducing cysteine rich protein with Kazal motifs (RECK), E-cadherin (E-cad) and down-regulate the expression of matrix metalloproteinases-2 (MMP-2), MMP-9, MMP-14 and Rhoc.
    CONCLUSIONS:
    In conclusion, Raddeanin A inhibits proliferation of human GC cells, induces their apoptosis and inhibits the abilities of invasion, migration and adhesion, exhibiting potential to become antitumor drug.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.1147 mL 5.5735 mL 11.1469 mL 22.2938 mL 27.8673 mL
    5 mM 0.2229 mL 1.1147 mL 2.2294 mL 4.4588 mL 5.5735 mL
    10 mM 0.1115 mL 0.5573 mL 1.1147 mL 2.2294 mL 2.7867 mL
    50 mM 0.0223 mL 0.1115 mL 0.2229 mL 0.4459 mL 0.5573 mL
    100 mM 0.0111 mL 0.0557 mL 0.1115 mL 0.2229 mL 0.2787 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
    金盏花苷E; Calenduloside E CFN91169 26020-14-4 C36H56O9 = 632.8 10mg QQ客服:2159513211
    地肤子皂苷Ic; Momordin Ic CFN99726 96990-18-0 C41H64O13 = 764.93 20mg QQ客服:2159513211
    姜状三七苷R1; Zingibroside R1 CFN92517 80930-74-1 C42H66O14 = 795.0 5mg QQ客服:1457312923
    次皂甙元CP4; Prosapogenin CP4 CFN90391 75799-18-7 C46H74O15 = 866.50 5mg QQ客服:1413575084
    竹节香附素A; Raddeanin A CFN99985 89412-79-3 C47H76O16 = 897.11 20mg QQ客服:2159513211
    Hederacolchiside A1; Hederacolchiside A1 CFN94808 106577-39-3 C47H76O16 = 897.10 20mg QQ客服:3257982914
    旱莲苷D; Ecliptasaponin D CFN90619 206756-04-9 C36H58O9 = 634.84 20mg QQ客服:1413575084
    旱莲苷A; Ecliptasaponin A CFN93253 78285-90-2 C36H58O9 = 634.9 20mg QQ客服:215959384
    葳岩仙皂苷A; Cauloside A CFN96440 17184-21-3 C35H56O8 = 604.81 10mg QQ客服:1413575084
    常春藤皂甙元-3-O-(2-O-乙酰基-α-L-吡喃阿拉伯糖甙); Hederagenin 3-O-(2-O-acetyl-alpha-L-arabinopyranoside) CFN95355 87562-05-8 C37H58O9 = 646.9 10mg QQ客服:1413575084

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