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  • 中药标准品生产商,产品定制服务
  • 曲美替尼

    Trametinib (GSK1120212)

    曲美替尼
    产品编号 CFN60051
    CAS编号 871700-17-3
    分子式 = 分子量 C26H23FIN5O4 = 615.39
    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
    曲美替尼 CFN60051 871700-17-3 1mg QQ客服:2159513211
    曲美替尼 CFN60051 871700-17-3 5mg QQ客服:2159513211
    曲美替尼 CFN60051 871700-17-3 10mg QQ客服:2159513211
    曲美替尼 CFN60051 871700-17-3 20mg QQ客服:2159513211
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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
  • Guangzhou Institutes of Biomedicine and Health (China)
  • Kamphaengphet Rajabhat University (Thailand)
  • Universiti Sains Malaysia (Malaysia)
  • Monash University Sunway Campus (Malaysia)
  • Aarhus University (Denmark)
  • University of Hawaii Cancer Center (USA)
  • Northeast Normal University Changchun (China)
  • Universidad de Ciencias y Artes de Chiapas (Mexico)
  • Chulalongkorn University (Thailand)
  • University of Wisconsin-Madison (USA)
  • University of Ioannina (Greece)
  • Universidade Federal de Pernambuco (UFPE) (Brazil)
  • Seoul National University of Science and Technology (Korea)
  • Aveiro University (Portugal)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Processes2021, 9(1), 153;
  • Biomed Pharmacother.2022, 145:112410.
  • The Pharmaceutical Society of Japan2018, 138(4):571-579
  • Int J Biol Macromol.2021, 199:189-200.
  • Appl. Sci. 2021, 11(23),11099.
  • Vietnam Journal of Food Control.2022, 5(3):pp.488-497.
  • Pharmacol Rep.2019, 71(2):289-298
  • The Japan Society for Analytical Chemistry2017, 613-617
  • Front Microbiol.2022, 12:833233.
  • Phytomedicine.2023, 116:154841.
  • Life Sci.2023, 317:121458.
  • Molecules.2024, 29(5):1050.
  • Antioxidants (Basel).2022, 11(12):2327.
  • Oxid Med Cell Longev2020, 12
  • Cardiovasc Toxicol.2021, 21(11):947-963.
  • Nat Prod Commun.2014, 9(5):679-82
  • Cancer Lett. 2023, 18:216584.
  • Sains Malaysiana2024, 53(2):397-408.
  • Acta Physiologiae Plantarum2016, 38:7
  • Psychopharmacology (Berl).2020, 10.1007
  • Molecules.2022, 27(19):6681.
  • J Adv Res.2019, 17:85-94
  • Cells. 2023, 12(15):1934.
  • ...
  • 生物活性
    Description: Trametinib (GSK1120212) is a highly specific and potent MEK1/2 inhibitor with IC50 of 0.92 nM/1.8 nM in cell-free assays, no inhibition of the kinase activities of c-Raf, B-Raf, ERK1/2. Trametinib activates autophagy and induces apoptosis.
    Targets: MEK1/2 | Autophagy
    In vivo:
    Inflamm Res,2012 May;61(5):445-54.
    Suppressive effect of an orally active MEK1/2 inhibitor in two different animal models for rheumatoid arthritis: a comparison with leflunomide.[Pubmed: 22245957]
    To examine the effects of a mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2-inhibitor, JTP-74057, on inflammatory arthritis development, and compare its anti-arthritic effect with leflunomide.
    METHODS AND RESULTS:
    Human, mouse, and rat peripheral blood mononuclear cells (PBMCs) were used. Lewis rats and DBA/1J mice were used for animal models.JTP-74057 was tested between 0.1-100 nM in in-vitro studies. JTP-74057 (0.01-0.3 mg/kg) and leflunomide (2-10 mg/kg) were administered orally in vivo. PBMCs were stimulated with lipopolysaccharide. Adjuvant-induced arthritis (AIA) and type II collagen-induced arthritis (CIA) was induced in Lewis rats or DBA1/J mice, respectively. JTP-74057 blocked tumor necrosis factor-α and interleukin-6 production from PBMCs. AIA and CIA development were suppressed almost completely by 0.1 mg/kg of JTP-74057 or 10 mg/kg of leflunomide. In the CIA, JTP-74057, but not leflunomide, suppressed collagen-reactive T-cell proliferation ex vivo, whereas leflunomide, but not JTP-74057, suppressed anti-collagen antibody production.
    CONCLUSIONS:
    JTP-74057 exerts potent anti-arthritic effects with a different profile from leflunomide, suggesting that JTP-74057 may be useful as a new therapeutic reagent in the treatment of rheumatoid arthritis.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.625 mL 8.1249 mL 16.2499 mL 32.4997 mL 40.6246 mL
    5 mM 0.325 mL 1.625 mL 3.25 mL 6.4999 mL 8.1249 mL
    10 mM 0.1625 mL 0.8125 mL 1.625 mL 3.25 mL 4.0625 mL
    50 mM 0.0325 mL 0.1625 mL 0.325 mL 0.65 mL 0.8125 mL
    100 mM 0.0162 mL 0.0812 mL 0.1625 mL 0.325 mL 0.4062 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
    印楝素; Nimbin CFN97722 5945-86-8 C30H36O9 = 540.61 5mg QQ客服:2159513211
    山药素 V; Batatasin V CFN95320 65817-45-0 C17H20O4 = 288.3 5mg QQ客服:3257982914
    金线莲苷; Kinsenoside CFN93288 151870-74-5 C10H16O8 = 264.2 20mg QQ客服:1457312923
    龙胆根素; Gentisin CFN89233 437-50-3 C14H10O5 = 258.22 5mg QQ客服:1413575084

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