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  • 白头翁皂苷D

    Pulsatilla saponin D

    白头翁皂苷D
    产品编号 CFN80453
    CAS编号 848784-85-0
    分子式 = 分子量 C47H76O17 = 913.10
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The herbs of Pulsatilla koreana
    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
    白头翁皂苷D CFN80453 848784-85-0 1mg QQ客服:2056216494
    白头翁皂苷D CFN80453 848784-85-0 5mg QQ客服:2056216494
    白头翁皂苷D CFN80453 848784-85-0 10mg QQ客服:2056216494
    白头翁皂苷D CFN80453 848784-85-0 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
  • Korea Institute of Oriental Medicine (Korea)
  • VIT University (India)
  • FORTH-IMBB (Greece)
  • University of Fribourg (Switzerland)
  • Massachusetts General Hospital (USA)
  • Seoul National University of Science and Technology (Korea)
  • The Ohio State University (USA)
  • Helmholtz Zentrum München (Germany)
  • Monash University Malaysia (Malaysia)
  • Melbourne University (Australia)
  • Stanford University (USA)
  • Florida International University (USA)
  • Universiti Sains Malaysia (Malaysia)
  • Uniwersytet Gdański (Poland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Microchemical Journal2024: 196:109676.
  • Braz J Med Biol Res. 2016, 49(7)
  • Oxid Med Cell Longev.2021, 2021:6647107.
  • Appl. Sci. 2021, 11(22), 10552
  • Hum Exp Toxicol.2017, 36(11):1169-1176
  • Auburn University2015, 1-58
  • J Nat Prod.2022, doi: 10.1021
  • University of Guelph2021, 12.
  • Korean J. Crop Sci.2018, 63(2):131-139
  • Vietnam J. Chemistry2022, 60(2):211-222
  • FEBS Lett.2015, 589(1):182-7
  • Plant Direct.2021, 5(4):e00318.
  • J Cell Mol Med.2023, 27(10):1423-1435.
  • Antioxidants (Basel).2021, 10(8):1300.
  • Int J Mol Sci.2019, 20(21):E5488
  • QASCF2022, 14(4).
  • Gene.2022, 815:146178.
  • Journal of Functional Foods2021, 84:104581
  • Oxid Med Cell Longev.2021, 2021:4883398.
  • Molecules.2021, 26(19):6032.
  • J Ethnopharmacol.2019, 236:31-41
  • Applied Biological Chemistry2022, 71:s13765-022-00743-5.
  • Plant J.2017, 90(3):535-546
  • ...
  • 生物活性
    Description: Pulsatilla saponin D exhibits anticancer activities in various cancer types, it Inhibits autophagic flux and synergistically enhances the anticancer activity of chemotherapeutic agents against HeLa cells.Pulsatilla saponin D has strong haemolytic activity.
    Targets: ERK | mTOR | Autophagy
    In vitro:
    J Nat Prod. 2018 Mar 23;81(3):465-474.
    Cytotoxicity, Hemolytic Toxicity, and Mechanism of Action of Pulsatilla Saponin D and Its Synthetic Derivatives.[Pubmed: 29131631]
    The strong hemolytic toxicity of Pulsatilla saponin D (1, HD50 6.3 μM) has hampered its clinical development as an injectable anticancer agent.
    CONCLUSIONS:
    To combat this challenge, 17 new derivatives of 1 with ring C, C-28, or C-3 modifications were synthesized and evaluated for cytotoxicity against several selected human tumor lines, as well as for hemolytic toxicity against rabbit erythrocytes. Structure-activity relationship (SAR) and structure-toxicity relationship (STR) correlations were also elucidated. Compared to the lead compound 1, the hemolytic activity of all 17 derivatives dropped dramatically. Notably, compound 14 exhibited significant cytotoxicity toward A549 human lung cancer cells (IC50 2.8 μM) in a dose-dependent manner without hemolytic toxicity (HD50 > 500 μM). Molecular studies indicated that 14 induced typical G1 cell cycle arrest and apoptosis in A549 cells, and Western blot assays suggested that both intrinsic and extrinsic apoptosis pathways were activated by 14.
    CONCLUSIONS:
    Collectively, compound 14 may merit further development as a potential anti-lung cancer agent.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.0952 mL 5.4759 mL 10.9517 mL 21.9034 mL 27.3793 mL
    5 mM 0.219 mL 1.0952 mL 2.1903 mL 4.3807 mL 5.4759 mL
    10 mM 0.1095 mL 0.5476 mL 1.0952 mL 2.1903 mL 2.7379 mL
    50 mM 0.0219 mL 0.1095 mL 0.219 mL 0.4381 mL 0.5476 mL
    100 mM 0.011 mL 0.0548 mL 0.1095 mL 0.219 mL 0.2738 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E; Pulchinenoside E CFN80291 366814-43-9 C65H106O31 = 1383.534 5mg QQ客服:3257982914
    3alpha-Acetoxy-20-oxo-29-norlupane-23,28-dioic acid; 3alpha-Acetoxy-20-oxo-29-norlupane-23,28-dioic acid CFN96240 262272-76-4 C31H46O7 = 530.7 5mg QQ客服:2159513211
    3alpha-Acetoxy-20(29)-lupene-23,28-dioic acid; 3alpha-Acetoxy-20(29)-lupene-23,28-dioic acid CFN89222 83725-41-1 C32H48O6 = 528.73 5mg QQ客服:215959384
    Acantrifoic acid A; Acantrifoic acid A CFN96223 654663-85-1 C32H48O7 = 544.7 5mg QQ客服:215959384
    苦艾素; Bacosine CFN70298 198014-94-7 C30H48O3 = 456.7 5mg QQ客服:3257982914
    白桦脂酸; Betulinic acid CFN98706 472-15-1 C30H48O3 = 456.7 20mg QQ客服:1413575084
    桦木酸甲酯; Betulinic acid methyl ester CFN91073 2259-06-5 C31H50O3 = 470.7 10mg QQ客服:1457312923
    圆齿火棘酸; Pyracrenic acid CFN89164 80832-44-6 C39H54O6 = 618.85 5mg QQ客服:2159513211
    苦苏花皂苷C; Cussosaponin C CFN90772 366814-42-8 C59H96O25 = 1204 5mg QQ客服:3257982914
    路路通酸; Betulonic acid CFN98682 4481-62-3 C30H46O3 = 454.7 20mg QQ客服:2056216494

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