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  • 鬼臼毒素

    Podophyllotoxin

    鬼臼毒素
    产品编号 CFN99168
    CAS编号 518-28-5
    分子式 = 分子量 C22H22O8 = 414.41
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Lignans
    植物来源 The roots of Dysosma versipellis (Hance) M.Cheng ex Ying.
    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
    鬼臼毒素 CFN99168 518-28-5 10mg QQ客服:3257982914
    鬼臼毒素 CFN99168 518-28-5 20mg QQ客服:3257982914
    鬼臼毒素 CFN99168 518-28-5 50mg QQ客服:3257982914
    鬼臼毒素 CFN99168 518-28-5 100mg QQ客服:3257982914
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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
  • Medical University of South Carolina (USA)
  • Donald Danforth Plant Science Center (USA)
  • University of Toulouse (France)
  • Worcester Polytechnic Institute (USA)
  • Max-Planck-Insitut (Germany)
  • Instituto de Investigaciones Agropecuarias (Chile)
  • Universidade do Porto (Portugal)
  • Center for protein Engineering (CIP) (Belgium)
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  • University of Fribourg (Switzerland)
  • Instytut Nawozów Sztucznych w Pu?awach (Poland)
  • Colorado State University (USA)
  • University of Hertfordshire (United Kingdom)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Molecules2020, 25(4):892
  • South African J of Botany2020, 135:50-57
  • J Enzyme Inhib Med Chem.2019, 34(1):134-143
  • Int J Mol Sci.2022, 23(13):7115.
  • Front Pharmacol.2019, 10:1355
  • Natural Product Communications2020, doi: 10.1177.
  • Talanta.2022, 249:123645.
  • Fitoterapia.2018, 124:92-102
  • Food Funct.2022, doi: 10.1039
  • RSC Advances2017, 86
  • Metabolites.2020, 10(12):497.
  • Curr Issues Mol Biol.2022, 44(10):5106-5116.
  • Biomolecules.2020, 10(2):E184
  • Int J Mol Sci.2022, 23(11):6104.
  • Int J Mol Sci.2017, 18(5)
  • Nat Prod Communications2018, 10.1177
  • J Am Soc Mass Spectrom.2021, 32(5):1205-1214.
  • Sci Rep.2015, 5:13194
  • Plants (Basel).2022, 11(16):2126.
  • J Ethnopharmacol.2019, 235:406-414
  • Research on Crops.2017, 18(3):569
  • Molecules.2019, 24(16):E2985
  • Biochem Systematics and Ecology2017, 11-18
  • ...
  • 生物活性
    Description: Podophyllotoxin(Podofilox ) is a potent inhibitor of microtubule assembly and DNA topoisomerase II. Podophyllotoxin has antitumor and antiviral properties, but it also shows cytotoxicity for normal cells and hence side effects derived from its lack of selectivity against tumoral cells.
    Targets: Topoisomerase | MMP(e.g.TIMP)
    In vitro:
    Anticancer Agents Med Chem. 2014 Nov 30.
    Recent Developments Towards Podophyllotoxin Congeners as Potential Apoptosis Inducers.[Pubmed: 25469512]
    Podophyllotoxin, a lignan extracted from rhizomes of Podophyllum species, is a well established lead in the development of new chemical agents for the treatment of cancer. Its semi-synthetic variant, etoposide is an anticancer drug which inhibits DNA topoisomerase II causing cell cycle arrest in the S the phase. Its clinical success and intriguing mode of action made it a much sought after skeleton for the development of better antitumor agents. Modifications were made at several positions of its skeleton with the aim to either improve its potency or to overcome drug resistance. In recent years, the structurally modified podophyllotoxins have been investigated for their apoptosis inducing ability. Although numerous reviews emphasized the occurrence, synthesis and applications of podophyllotoxins, the recent progress towards development of structurally modified podophyllotoxins possessing apoptosis inducing ability has not been previously reviewed.
    CONCLUSIONS:
    Therefore the present review focuses on the studies carried out in the design and synthesis of new podophyllotoxin derivatives and their evaluation as apoptosis inducers.
    Exp Ther Med. 2014 May;7(5):1317-1322. Epub 2014 Mar 6.
    Apoptosis of human gastric cancer SGC-7901 cells induced by podophyllotoxin.[Pubmed: 24940431]
    Numerous studies have demonstrated that podophyllotoxin and its derivatives exhibit antitumor effects. The aim of the present study was to investigate SGC-7901 cell apoptosis and the underlying mechanism induced by podophyllotoxin. SGC-7901 cells were treated with varying concentrations of podophyllotoxin.
    METHODS AND RESULTS:
    MTT assays and flow cytometry were used to evaluate the effects of podophyllotoxin on the proliferation and apoptosis of SGC-7901 cells, while fluorescence inverted microscopy was used to observe the morphology of SGC-7901 cells that had been dyed with Hoechst 33258. In addition, laser scanning confocal microscopy was used to analyze the mitochondrial membrane potential (MMP) of SGC-7901 cells dyed with Rhodamine 123. Western blotting was performed to analyze the expression levels of cytochrome c (cyt-c), caspase-9 and caspase-3 in the SGC-7901 cells. The results indicated that podophyllotoxin was capable of inhibiting growth and inducing the apoptosis of SGC-7901 cells in a dose-dependent manner, causing cell cycle arrest at the G2/M phase. After 48 h of treatment, the apoptotic morphology of SGC-7901 cells was clear, exhibiting cell protuberance, concentrated cytoplasms and apoptotic bodies. Following 24 h of treatment, the MMP of the SGC-7901 cells decreased. In addition, after 48 h, the expression of cyt-c was shown to be upregulated, while the expression levels of pro-caspase-9 and pro-caspase-3 in the SGC-7901 cells were shown to be downregulated.
    CONCLUSIONS:
    In conclusion, apoptosis can be induced in SGC-7901 cells by podophyllotoxin, potentially via a mitochondrial pathway, indicating that podophyllotoxin may be a potent agent for cancer treatment.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.4131 mL 12.0653 mL 24.1307 mL 48.2614 mL 60.3267 mL
    5 mM 0.4826 mL 2.4131 mL 4.8261 mL 9.6523 mL 12.0653 mL
    10 mM 0.2413 mL 1.2065 mL 2.4131 mL 4.8261 mL 6.0327 mL
    50 mM 0.0483 mL 0.2413 mL 0.4826 mL 0.9652 mL 1.2065 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
    Justicidinoside C; Justicidinoside C CFN95712 177912-23-1 C27H26O12 = 542.5 5mg QQ客服:2056216494
    山荷叶素; Diphyllin CFN91906 22055-22-7 C21H16O7 = 380.35 20mg QQ客服:2056216494
    山荷叶素 O-葡萄糖苷; Diphyllin O-glucoside CFN91907 30021-77-3 C27H26O12 = 542.49 5mg QQ客服:1457312923
    爵床苷E; Procumbenoside E CFN95713 220182-12-7 C36H40O19 = 776.7 5mg QQ客服:1457312923
    爵床酯定A; Justicidin A CFN95702 25001-57-4 C22H18O7 = 394.4 5mg QQ客服:1413575084
    金不换萘酚甲醚; Chinensinaphthol methyl ether CFN95703 53965-11-0 C22H18O7 = 394.4 5mg QQ客服:3257982914
    新爵床素 B; Justicidin C(Neojusticin B) CFN95704 17803-12-2 C22H18O7 = 394.4 5mg QQ客服:2159513211
    新爵床素 A; Justicidin D(Neojusticin A) CFN95705 27041-98-1 C21H14O7 = 378.3 5mg QQ客服:1457312923
    Marginatoxin; Marginatoxin CFN95174 1422536-56-8 C22H22O7 = 398.4 10mg QQ客服:1413575084
    双细辛酮2; gamma-Diasarone CFN97279 80434-33-9 C24H32O6 = 416.5 5mg QQ客服:3257982914

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