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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:2056216494
    竹节香附素A CFN99985 89412-79-3 20mg QQ客服:2056216494
    竹节香附素A CFN99985 89412-79-3 50mg QQ客服:2056216494
    竹节香附素A CFN99985 89412-79-3 100mg 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)

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  • University of the Basque Country (Spain)
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  • Kyushu University (Japan)
  • Indian Institute of Science (India)
  • St. Jude Children Research Hospital (USA)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Ethnopharmacol.2020, 249:112396
  • Toxicol In Vitro.2023, 86:105521.
  • Braz J Med Biol Res. 2016, 49(7)
  • Antioxidants.2022, 11(3):592.
  • Oxid Med Cell Longev2020, 12
  • J Chromatogr A.2022, 1685:463640.
  • Processes2022, 10(10), 2008.
  • The Korea Journal of Herbology2016, 29-35
  • Acta Pharm Sin B.2015, 5(4):323-9.
  • Drug Chem Toxicol.2020, 1-14.
  • Int Immunopharmacol.2023, 7:127:111322.
  • Food Chem.2020, 313:126079
  • Kasetsart University2022, ethesis.1144.
  • HortTechnology2016, 26(6):816-819
  • Molecules.2022, 27(7):2093.
  • Antioxidants (Basel).2022, 11(12):2411.
  • Journal of Phytopathology2021, 169,Issue11-12.
  • Food Research International2023, 113792.
  • Food Chem.2016, 191:81-90
  • Food Chem.2018, 262:78-85
  • J Biotechnol.2020, 318:10-19.
  • Front Plant Sci.2023, 14:1207940.
  • J Ethnopharmacol.2017, 206:327-336
  • ...
  • 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
    白头翁皂苷E2; Pulchinenoside E2 CFN80362 244202-36-6 C53H86O21 = 1059.24 5mg QQ客服:2159513211
    Dipsacobioside; Dipsacobioside CFN94827 123350-57-2 C41H66O12 = 750.96 5mg QQ客服:3257982914
    丝石竹皂苷元; Gypsogenin CFN91485 639-14-5 C30H46O4 = 470.7 5mg QQ客服:1457312923
    丝石竹皂苷元-3-O-β-D-葡萄糖醛酸甲酯; Methyl gypsogenin 3-O-beta-D-glucuronopyranoside CFN90727 96553-02-5 C37H56O10 = 660.9 20mg QQ客服:215959384
    贝萼皂苷元 3-O-beta-D-吡喃葡萄糖苷; Bayogenin 3-O-beta-D-glucopyranoside CFN90996 104513-86-2 C36H58O10 = 650.84 5mg QQ客服:3257982914
    细叶远志皂苷; Tenuifolin CFN98157 20183-47-5 C36H56O12 = 680.37 20mg QQ客服:1457312923
    红背银莲花皂甙20; Raddeanoside 20 CFN90659 335354-79-5 C47H76O17 = 913.1 5mg QQ客服:1457312923
    刺五加皂苷B; Ciwujianoside B CFN99983 114902-16-8 C58H92O25 = 1189.35 20mg QQ客服:2159513211
    Eupteleasaponin I; Eupteleasaponin I CFN90959 290809-29-9 C52H82O21 = 1043.21 5mg QQ客服:1413575084
    Nudicaucin A; Nudicaucin A CFN90962 211815-97-3 C46H72O17 = 897.07 5mg QQ客服:1413575084

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