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  • 重楼皂苷G

    Polyphyllin G

    重楼皂苷G
    产品编号 CFN99955
    CAS编号 76296-75-8
    分子式 = 分子量 C51H84O22 = 1049.22
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Steroids
    植物来源 The rhizomes of Paris yunnanensis Franch.
    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
    重楼皂苷G CFN99955 76296-75-8 1mg QQ客服:1413575084
    重楼皂苷G CFN99955 76296-75-8 5mg QQ客服:1413575084
    重楼皂苷G CFN99955 76296-75-8 10mg QQ客服:1413575084
    重楼皂苷G CFN99955 76296-75-8 20mg 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
  • Complutense University of Madrid (Spain)
  • Medical University of South Carolina (USA)
  • University of Wollongong (Australia)
  • University of Stirling (United Kingdom)
  • Istanbul University (Turkey)
  • Max Rubner-Institut (MRI) (Germany)
  • The Australian National University (Australia)
  • University of Eastern Finland (Finland)
  • Kamphaengphet Rajabhat University (Thailand)
  • Universita' Degli Studi Di Cagliari (Italy)
  • Vin?a Institute of Nuclear Sciences (Serbia)
  • Yale University (USA)
  • University of Padjajaran (Indonesia)
  • University of Zurich (Switzerland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Research Square2021, 10.21203.
  • Neurochem Int.2018, 121:114-124
  • Phytomedicine.2018, 38:12-23
  • Int. J. Mol. Sci.2022, 23(19), 11900.
  • Research Square2023, 2883170.
  • Br J Pharmacol.2020, 10.1111
  • J Liq Chromatogr R T2018, 41(12):761-769
  • Antioxidants (Basel).2022, 11(12):2496.
  • Drug Chem Toxicol.2020, 1-14.
  • Planta Med.2019, 85(4):347-355
  • Molecules.2021, 26(13):4081.
  • BMC Complement Altern Med.2019, 19(1):339
  • JMSACL2023, 09.002
  • Sci Rep. 2018, 1-9
  • Front Pharmacol.2021, 12:764297.
  • University of Central Lancashire2017, 20472
  • Front Pharmacol.2020, 11:566490.
  • RSC Adv.2023, 13(9):6317-6326.
  • Phytomedicine.2018, 41:62-66
  • Molecules.2016, 21(6)
  • Applied Physics B2021, 127(92).
  • Chemistry of Natural Compounds2018, 54(3):572-576
  • Front Pharmacol.2022, 13:906763.
  • ...
  • 生物活性
    Description: Polyphyllin G has been shown to have strong anticancer activities in a wide variety of human cancer cell lines, it also shows significant anthelmintic activity against Dactylogyrus intermedius with EC50 values of 1.2 mg L(-1) and the acute toxicities (LC50) values of 2.9 mg L(-1).
    Targets: Caspase | Bcl-2/Bax | Akt | ERK | JNK | p38MAPK | Autophagy | Antifection
    In vitro:
    Phytomedicine. 2016 Dec 1;23(13):1545-1554.
    Polyphyllin G induces apoptosis and autophagy cell death in human oral cancer cells.[Pubmed: 27823618]
    Polyphyllin G (also called polyphyllin VII), extract from rhizomes of Paris yunnanensis Franch, has been shown to have strong anticancer activities in a wide variety of human cancer cell lines. However, the underlying influences of autophagy in human oral squamous cell carcinoma (OSCC) remain unclear.
    METHODS AND RESULTS:
    In this study, the roles of apoptosis and autophagy in polyphyllin G-induced death in human oral cancer cells were investigated. Moreover, the molecular mechanism of the anticancer effects of polyphyllin G in human oral cancer cells was investigated. The results revealed that polyphyllin G significantly inhibited cell proliferation in human oral cancer cells; it dose-dependently induced apoptosis in SAS and OECM-1 cells through caspase-3, -8, and -9 activation and poly (ADP-ribose) polymerase cleavage. In addition, changes were observed in Bcl-2 and proapoptosis-related protein expression in different human oral cancer cell lines. The expression of both LC3-II and beclin-1 was markedly increased, suggesting the induction of autophagy in polyphyllin G-treated oral cells. To further clarify whether polyphyllin G-induced apoptosis and autophagy depended on Akt/extracellular signal-regulated kinases (ERK)/c-Jun N-terminal kinases (JNK)/p38 mitogen-activated protein kinases (MAPK) signaling pathways, the cells were cotreated with inhibitors. The results demonstrated polyphyllin G-induced apoptosis in oral cells through the activation of ERK, Akt, p38 MAPK, and JNK, whereas ERK and JNK accounted for polyphyllin G-induced autophagy.
    CONCLUSIONS:
    This study is the first to demonstrate apoptosis and autophagy during polyphyllin G-induced cell death in human oral cancer cell lines. These results suggest that polyphyllin G is a promising candidate for developing antitumor drugs targeting human oral squamous cell carcinoma.
    Arch Biochem Biophys . 2018 Apr 15;644:93-99.
    Polyphyllin G exhibits antimicrobial activity and exerts anticancer effects on human oral cancer OECM-1 cells by triggering G2/M cell cycle arrest by inactivating cdc25C-cdc2[Pubmed: 29352966]
    Abstract Plant natural products have long been considered to be important sources of bioactive molecules. A large number of antimicrobial and anticancer agents have been isolated form plants. In the present study we evaluated the antimicrobial and anticancer activity of a plant derived secondery metabolite, Polyphyllin G. The results of antibacterial assays showed that Polyphyllin G prevented the growth of both Gram-positive and Gram-negative bacteria with minimum inhibitory concentrations (MICs) ranging from 13.1 to 78 μg/ml. Antifungal activity measured as inhibition of mycelium growth ranged between 38.32 and 56.50%. Further Polyphyllin G was also evaluated against a panel of cancer cell lines. The IC50 of Polyphyllin G ranged from 10 to 65 μM. However the IC50 of Polyphyllin G was found to be comparatively high (120 μM) against the normal FR2 cancer cell line. The lowest IC50 of 10 μM was found against the oral cancer cell line OECM-1. Therefore further studies were carried out on this cell line only. Our results indicated that Polyphyllin G induced cell arrest in oral cancer OECM-1 cells by inactivation of cdc25C-cdc22 via ATM-Chk 1/2 stimulation. Therefore, we propose that Polyphyllin G might prove a lead molecule in the management of oral cancers and at the same time may prevent the growth of opportunistic microbes. Keywords: Anticancer; Antimicrobial; Cell cycle arrest; Metastasis; Oral cancer; Polyphyllin G.
    In vivo:
    Parasitology. 2013 Jul;140(8):952-8.
    Identification of compounds from Paris polyphylla (ChongLou) active against Dactylogyrus intermedius.[Pubmed: 23552446]
    The present study was designated to ascertain the anthelmintic activity of the rhizomes of Paris polyphylla and to isolate and characterize the active constituents.
    METHODS AND RESULTS:
    The methanol extract from rhizomes of P. polyphylla showed significant anthelmintic activity against Dactylogyrus intermedius with the median effective concentration (EC50) 22.5 mg L(-1). Based on this finding, the methanol extract was fractionated by silica gel column chromatography in a bioassay-guided fractionation yielding 2 bioactive compounds, the structures of these compounds were elucidated as formosanin C and polyphyllin VII(Polyphyllin G). The in vivo tests revealed that formosanin C and polyphyllin VII were significantly effective against D. intermedius with EC50 values of 0.6 and 1.2 mg L(-1), respectively. The acute toxicities (LC50) of formosanin C and polyphyllin VII for grass carp were 2.8 and 2.9 mg L(-1), respectively.
    CONCLUSIONS:
    The overall results provide important information for the potential application of formosanin C and polyphyllin VII in the therapy of serious infection caused by D. intermedius.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 0.9531 mL 4.7654 mL 9.5309 mL 19.0618 mL 23.8272 mL
    5 mM 0.1906 mL 0.9531 mL 1.9062 mL 3.8124 mL 4.7654 mL
    10 mM 0.0953 mL 0.4765 mL 0.9531 mL 1.9062 mL 2.3827 mL
    50 mM 0.0191 mL 0.0953 mL 0.1906 mL 0.3812 mL 0.4765 mL
    100 mM 0.0095 mL 0.0477 mL 0.0953 mL 0.1906 mL 0.2383 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
    原皂苷Pa; Parisaponin I CFN90702 561007-63-4 C50H82O22 = 1034.0 5mg QQ客服:2159513211
    原皂苷Pb; Dichotomin CFN90703 53093-47-3 C57H94O26 = 1195.34 5mg QQ客服:1457312923
    知母皂苷B; Anemarsaponin B CFN99532 139051-27-7 C45H74O18 = 903.04 20mg QQ客服:1457312923
    知母皂苷BIII; Anemarsaponin BIII CFN90778 142759-74-8 C45H74O18 = 903.1 5mg QQ客服:1413575084
    知母皂苷C; Timorsaponin C CFN90779 185432-00-2 C45H74O18 = 903.1 5mg QQ客服:2159513211
    伪原皂苷Pa; Parisyunnanoside B CFN90704 945865-37-2 C50H80O21 = 1016.0 10mg QQ客服:2056216494
    伪原薯蓣皂苷; Pseudoprotodioscin CFN90694 102115-79-7 C51H82O2 = 1031.18 20mg QQ客服:1457312923
    黄山药皂苷C; Dioscoreside C CFN95345 C52H84O22 = 1061.2 5mg QQ客服:2056216494
    黄山药皂苷E; Dioscoreside E CFN95346 435321-73-6 C52H84O23 = 1077.2 5mg QQ客服:2056216494
    蒺藜皂苷K; Terrestrosin K CFN90822 193605-07-1 C51H82O24 = 1079.2 10mg QQ客服:215959384

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