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  • (-)-β-盾叶鬼臼素

    (-)-beta-Peltatin

    (-)-β-盾叶鬼臼素
    产品编号 CFN92699
    CAS编号 518-29-6
    分子式 = 分子量 C22H22O8 = 414.4
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Lignans
    植物来源 The herbs of Podophyllum peltatum
    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
    (-)-β-盾叶鬼臼素 CFN92699 518-29-6 1mg QQ客服:1457312923
    (-)-β-盾叶鬼臼素 CFN92699 518-29-6 5mg QQ客服:1457312923
    (-)-β-盾叶鬼臼素 CFN92699 518-29-6 10mg QQ客服:1457312923
    (-)-β-盾叶鬼臼素 CFN92699 518-29-6 20mg QQ客服:1457312923
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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
  • Universiti Malaysia Pahang (Malaysia)
  • Auburn University (USA)
  • Max-Planck-Insitut (Germany)
  • University of Queensland (Australia)
  • Siksha O Anusandhan University (India)
  • University of Sao Paulo (Brazil)
  • Sapienza University of Rome (Italy)
  • Universidad Veracuzana (Mexico)
  • University of Brasilia (Brazil)
  • University of Illinois (USA)
  • Kitasato University (Japan)
  • China Medical University (Taiwan)
  • Universita' Degli Studi Di Cagliari (Italy)
  • Chinese University of Hong Kong (China)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Microbiol Biotechnol.2020, 30(2):178-186.
  • Current Topics in Nutraceutical Research2021, 19(1),p90-105.
  • Phytomedicine.2016, 23(4):331-9
  • Int J Mol Sci.2022, 23(11):6172.
  • J Mater Chem B.2019, 7(39):5896-5919
  • Indian J Pharm Sci.2022, 84(4): 874-882.
  • Trop J Pharm Res.2023, 22(3):283-288.
  • Front. Plant Sci.2022, 13:757852.
  • J Korean Med Ophthalmol Otolaryngol Dermatol2023, 36(1):1-20.
  • PLoS One.2020, 15(2):e0220084.
  • Phytochem Anal.2023, pca.3305.
  • Curr Issues Mol Biol.2023, ;45(2):1601-1612.
  • J Sci Food Agric.2023, 103(1):213-220.
  • Food Funct.2020, 11(2):1322-1333.
  • Pharmacol Rep.2019, 71(2):289-298
  • Neuropharmacology.2018, 131:68-82
  • Journal of Food Hygiene and Safety2019, 34(5):413-420
  • J Pharm Biomed Anal.2019, 164:119-127
  • Molecules.2018, 23(11):E2837
  • Nutrients.2020, 12(3):595.
  • Cytotechnology.2017, 69(5):765-773
  • Int Immunopharmacol.2023, 7:127:111322.
  • Mediators Inflamm.2016, 2016:7216912
  • ...
  • 生物活性
    Description: (-)-beta-Peltatin has antimitotic, and antineoplastic activities.
    In vitro:
    Pesticide Biochemistry and Physiology, 2002, 72(1):45-54.
    Aryltetralin Lignans Inhibit Plant Growth by Affecting the Formation of Mitotic Microtubular Organizing Centers.[Reference: WebLink]

    METHODS AND RESULTS:
    The aryltetralin lignans podophyllotoxin, α-peltatin, and β-peltatin((-)-beta-Peltatin ), their respective O-β-d-glucosides, and the semisynthetic derivative etoposide were tested for phytotoxicity. The aglycones were more potent inhibitors than their respective glucosides, and podophyllotoxin was the most active natural lignan tested. These compounds were more active against rye (Lolium multiflorum L.) and onion (Allium cepa L.) than lettuce (Lactuca sativa L.). The semisynthetic lignan etoposide was more active than any of the natural analogues and was phytotoxic to both monocotyledonous and dicotyledonous species. Inhibition of root growth was the main developmental response observed on plants tested with the lignans. At the cellular level, podophyllotoxin and etoposide caused similar symptoms in actively dividing meristematic cells of onion root tips. All phases of mitosis were inhibited by nearly 50%, relative to the controls. Both compounds also induced abnormal star anaphase chromosomal configurations.
    CONCLUSIONS:
    While the precise molecular mechanism of action of these compounds remains to be identified in plants, a primary effect is the alteration of the formation of the spindle microtubular organization centers, resulting in the formation of multiple spindle poles and an asymmetrical convergence of the chromosomes.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.4131 mL 12.0656 mL 24.1313 mL 48.2625 mL 60.3282 mL
    5 mM 0.4826 mL 2.4131 mL 4.8263 mL 9.6525 mL 12.0656 mL
    10 mM 0.2413 mL 1.2066 mL 2.4131 mL 4.8263 mL 6.0328 mL
    50 mM 0.0483 mL 0.2413 mL 0.4826 mL 0.9653 mL 1.2066 mL
    100 mM 0.0241 mL 0.1207 mL 0.2413 mL 0.4826 mL 0.6033 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
    山荷叶素; Diphyllin CFN91906 22055-22-7 C21H16O7 = 380.35 20mg QQ客服:1413575084
    山荷叶素 O-葡萄糖苷; Diphyllin O-glucoside CFN91907 30021-77-3 C27H26O12 = 542.49 5mg QQ客服:1413575084
    爵床苷E; Procumbenoside E CFN95713 220182-12-7 C36H40O19 = 776.7 5mg QQ客服:215959384
    爵床酯定A; Justicidin A CFN95702 25001-57-4 C22H18O7 = 394.4 5mg QQ客服:2056216494
    金不换萘酚甲醚; Chinensinaphthol methyl ether CFN95703 53965-11-0 C22H18O7 = 394.4 5mg QQ客服:1413575084
    新爵床素 B; Justicidin C(Neojusticin B) CFN95704 17803-12-2 C22H18O7 = 394.4 5mg QQ客服:1457312923
    新爵床素 A; Justicidin D(Neojusticin A) CFN95705 27041-98-1 C21H14O7 = 378.3 5mg QQ客服:3257982914
    Marginatoxin; Marginatoxin CFN95174 1422536-56-8 C22H22O7 = 398.4 10mg QQ客服:2056216494
    双细辛酮2; gamma-Diasarone CFN97279 80434-33-9 C24H32O6 = 416.5 5mg QQ客服:2056216494
    alpha-铁杉脂素; alpha-Conidendrin CFN97420 85699-62-3 C20H20O6 = 356.4 5mg QQ客服:2056216494

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