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  • 枸橼酸托法替尼

    Tofacitinib citrate

    枸橼酸托法替尼
    产品编号 CFN60039
    CAS编号 540737-29-9
    分子式 = 分子量 C16H20N6O.C6H8O7 = 504.49
    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
    枸橼酸托法替尼 CFN60039 540737-29-9 1mg QQ客服:2056216494
    枸橼酸托法替尼 CFN60039 540737-29-9 5mg QQ客服:2056216494
    枸橼酸托法替尼 CFN60039 540737-29-9 10mg QQ客服:2056216494
    枸橼酸托法替尼 CFN60039 540737-29-9 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
  • University of Bonn (Germany)
  • University of Bordeaux (France)
  • Seoul National University of Science and Technology (Korea)
  • Sant Gadge Baba Amravati University (India)
  • Macau University of Science and Technology (China)
  • Kamphaengphet Rajabhat University (Thailand)
  • Istanbul University (Turkey)
  • University of Maryland School of Medicine (USA)
  • Medizinische Universit?t Wien (Austria)
  • University of Toronto (Canada)
  • Chang Gung University (Taiwan)
  • Universitas Airlangga (Indonesia)
  • University of Auckland (New Zealand)
  • University of Dicle (Turkey)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Evid Based Complement Alternat Med.2022, 9767292,2.
  • Evid Based Complement Alternat Med.2020, 2020:9416962.
  • Preprints2017, 2017120176
  • J Nat Med.2022, 76(1):59-67.
  • Current Enzyme Inhibition2023, 19(1):55-64(10)
  • Molecules.2022, 27(7):2116.
  • Bio-protocol2018, 9(14):e3301
  • The Japan Society for Analy. Chem.2017, 66(8):613-617
  • LWT2021, 138:110397.
  • Int J Mol Sci.2018, 19(9):E2528
  • Int J Mol Sci.2019, 20(23):E6071
  • The Journal of Korean Medicine2023, 44(4):26-40.
  • J Appl Biol Chem2022, 65:343−348.
  • Phytomedicine.2022, 110:154597.
  • Anal Biochem.2019, 569:10-15
  • Nutr Res Pract.2020, 14(5):478-489.
  • Int J Mol Sci.2015, 16(8):18396-411
  • J Complement Integr Med.2024, jcim-2023-0177.
  • Toxicol Appl Pharmacol.2021, 427:115668.
  • Food Funct.2021, 12(4):1469-1481.
  • The Korea Journal of Herbology2019, 34(2):25-32
  • Antioxidants (Basel).2020, 9(11):1121.
  • J Ethnopharmacol.2020, 269:113752.
  • ...
  • 生物活性
    Description: Tofacitinib citrate (CP-690550 citrate) is a novel inhibitor of JAK with IC50 of 1 nM, 20 nM and 112 nM against JAK3, JAK2, and JAK1, respectively. Tofacitinib citrate has anti-infection activity.
    Targets: JAK1/JAK2/JAK3
    In vivo:
    J Leukoc Biol,2004 Dec;76(6):1248-55.
    The JAK3 inhibitor CP-690550 selectively reduces NK and CD8+ cell numbers in cynomolgus monkey blood following chronic oral dosing.[Pubmed: 15371489]
    Janus kinase 3 (JAK3) is a cytoplasmic tyrosine kinase associated with the common gamma chain, an integral component of cytokine receptors of the interleukin (IL)-2 family, including IL-4, -7, -9, -15, and -21. CP-690550 is a JAK3 inhibitor with immunosuppressive properties under development for transplantation.
    METHODS AND RESULTS:
    We evaluated alterations in circulating lymphocyte subsets in cynomolgus monkey blood following chronic (3-week), oral CP-690550 administration. Natural killer (NK) and CD8+ T cell numbers were reduced in a dose- and time-dependent manner; the latter was a primary effect on memory subsets. CD4+ T and B cell numbers were unaffected or slightly increased, respectively. NK cell numbers were reduced approximately 80% (vs. 35% in vehicle-treated animals) and returned to baseline levels within 3 weeks following treatment cessation. CD8+ T cells declined by a maximum 43% (vs. 25% for vehicle-treated animals) but rebounded significantly (300%) within 2 weeks after the last dose. Although CP-690550 did not result in reduction of CD4+ T cell number, these cells also increased (225%) within 2 weeks of treatment cessation. IL-15 is important for maintaining homeostasis of these cell types, and CP-690550 inhibited IL-15-induced CD69 expression in NK cells [inhibitory concentration 50% (IC50)=48.0+/-8.4 nM] and CD8+ T cells (IC50=16.2+/-1.5 nM).
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.9822 mL 9.911 mL 19.822 mL 39.644 mL 49.555 mL
    5 mM 0.3964 mL 1.9822 mL 3.9644 mL 7.9288 mL 9.911 mL
    10 mM 0.1982 mL 0.9911 mL 1.9822 mL 3.9644 mL 4.9555 mL
    50 mM 0.0396 mL 0.1982 mL 0.3964 mL 0.7929 mL 0.9911 mL
    100 mM 0.0198 mL 0.0991 mL 0.1982 mL 0.3964 mL 0.4955 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
    7-氧代脱氢枞醇; 7-Oxodehydroabietinol CFN98438 33980-71-1 C20H28O2 = 300.4 5mg QQ客服:3257982914
    去甲氧基矢车菊黄酮素; Desmethoxycentaureidin CFN98234 22934-99-2 C17H14O7 = 330.3 5mg QQ客服:2056216494
    告达亭苷元; Caudatin CFN99007 38395-02-7 C28H42O7 = 490.6 20mg QQ客服:1457312923
    大麻二醇酸; Cannabidiolic acid CFN99356 1244-58-2 C22H30O4 = 358.5 5mg QQ客服:2159513211

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