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  • 盐酸帕博西尼

    Palbociclib hydrochloride

    盐酸帕博西尼
    产品编号 CFN60047
    CAS编号 827022-32-2
    分子式 = 分子量 C24H29N7O2.HCl = 483.99
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源
    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
    盐酸帕博西尼 CFN60047 827022-32-2 1mg QQ客服:3257982914
    盐酸帕博西尼 CFN60047 827022-32-2 5mg QQ客服:3257982914
    盐酸帕博西尼 CFN60047 827022-32-2 10mg QQ客服:3257982914
    盐酸帕博西尼 CFN60047 827022-32-2 20mg 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
  • University of Oslo (Norway)
  • University of Wuerzburg (Germany)
  • University of Leipzig (Germany)
  • University of Mysore (India)
  • University of Lodz (Poland)
  • Griffith University (Australia)
  • National Cancer Center Research Institute (Japan)
  • Copenhagen University (Denmark)
  • Charles Sturt University (Denmark)
  • Wageningen University (Netherlands)
  • Universitas Airlangga (Indonesia)
  • National Cancer Institute (USA)
  • Julius Kühn-Institut (Germany)
  • University of British Columbia (Canada)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Processes2021, 9(11),2065.
  • Anat Rec2018, 24264
  • Molecules.2019, 24(4):E744
  • Cancers (Basel).2021, 13(6):1432.
  • Drug Des Devel Ther.2023, 17:2461-2479.
  • Phytother Res.2019, 33(4):1104-1113
  • Nutrients.2023, 15(4):950.
  • Int J Biol Macromol.2018, 112:1093-1103
  • Pharmaceutics.2023, 15(6):1771.
  • Analytical methods2019, 11(6)
  • Molecules.2019, 24(9):E1719
  • Pharmacia2024, 71:1-9.
  • Separations2021, 8(6),80.
  • Biochem Biophys Res Commun.2018, 505(1):194-200
  • J Cell Biochem.2018, 119(2):2231-2239
  • Theoretical and Experimental Plant Physiology 2022, 34,53-62
  • Plant Cell Physiol.2023, 64(7):716-728.
  • Nutrients.2017, 10(1)
  • LWT2020, 126:109313
  • Food Chem X.2024, 21:101127.
  • Journal of Mushroom2023, 21(4):215-221.
  • Molecules.2019, 24(2):E343
  • Int J Nanomedicine.2024, 19:1683-1697.
  • ...
  • 生物活性
    Description: Palbociclib (PD-0332991) HCl is a highly selective inhibitor of CDK4/6 with IC50 of 11 nM/16 nM in cell-free assays, respectively. It shows no activity against CDK1/2/5, EGFR, FGFR, PDGFR, InsR, etc.
    Targets: CDK4/6
    In vitro:
    Cancer Res,2008 Jul 15;68(14):5519-23.
    A novel therapeutic combination using PD 0332991 and bortezomib: study in the 5T33MM myeloma model.[Pubmed: 18632601]
    Multiple myeloma (MM) remains incurable partly because no effective cell cycle-based therapy has been available to both control tumor cell proliferation and synergize with cytotoxic killing. PD 0332991 is an orally active small molecule that potently and specifically inhibits Cdk4 and Cdk6. It has been shown to induce rapid G(1) cell cycle arrest in primary human myeloma cells and suppress tumor growth in xenograft models.
    METHODS AND RESULTS:
    To improve therapeutic targeting of myeloma progression, we combined tumor suppression by PD 0332991 with cytotoxic killing by bortezomib, a proteasome inhibitor widely used in myeloma treatment, in the immunocompetent 5T33MM myeloma model. We show that 5T33MM tumor cells proliferate aggressively in vivo due to expression of cyclin D2, elevation of Cdk4, and impaired p27(Kip1) expression, despite inhibition of Cdk4/6 by p18(INK4c) and the maintenance of a normal plasma cell transcription program. PD 0332991 potently inhibits Cdk4/6-specific phosphorylation of Rb and cell cycle progression through G(1) in aggressively proliferating primary 5T33MM cells, in vivo and ex vivo. This leads to tumor suppression and a significant improvement in survival. Moreover, induction of G(1) arrest by PD 0332991 sensitizes 5T33MM tumor cells to killing by bortezomib.
    CONCLUSIONS:
    Inhibition of Cdk4/6 by PD 0332991, therefore, effectively controls myeloma tumor expansion and sensitizes tumor cells to bortezomib killing in the presence of an intact immune system, thereby representing a novel and promising cell cycle-based combination therapy.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.0662 mL 10.3308 mL 20.6616 mL 41.3232 mL 51.654 mL
    5 mM 0.4132 mL 2.0662 mL 4.1323 mL 8.2646 mL 10.3308 mL
    10 mM 0.2066 mL 1.0331 mL 2.0662 mL 4.1323 mL 5.1654 mL
    50 mM 0.0413 mL 0.2066 mL 0.4132 mL 0.8265 mL 1.0331 mL
    100 mM 0.0207 mL 0.1033 mL 0.2066 mL 0.4132 mL 0.5165 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
    羟基积雪草苷; Madecassoside CFN99913 34540-22-2 C48H78O20 = 975.13 20mg QQ客服:1457312923
    五水棉子糖; Raffinose CFN90425 17629-30-0 C18H32O16(5H2O) = 594.51 20mg QQ客服:2056216494
    Cypellocarpin C; Cypellocarpin C CFN89273 294856-66-9 C26H32O11 = 520.53 5mg QQ客服:1413575084
    凡德他尼; Vandetanib CFN60163 443913-73-3 C22H24BrFN4O2 = 475.35 5mg QQ客服:3257982914

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