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S81263

RN486

源葉(MedMol) 99%
  • 英文名:
  • RN486
  • 別名:
  • 6-Cyclopropyl-8-fluoro-2-(2-hydroxymethyl-3-{1-methyl-5-[5-(4-methyl-piperazin-1-yl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-phenyl)-2H-isoquinolin-1-one; RN 486; QCR-5; 6-cyclopropyl-8-flu
  • CAS號(hào):
  • 1242156-23-5
  • 分子式:
  • C35H35FN6O3
  • 分子量:
  • 606.6892
品牌貨號(hào)產(chǎn)品規(guī)格價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 數(shù)量計(jì)量單位 加入購(gòu)物車...
源葉(MedMol) S81263-1mg 99% ¥130.00元 10 - - - EA 加入購(gòu)物車
源葉(MedMol) S81263-5mg 99% ¥210.00元 5 - - - EA 加入購(gòu)物車
源葉(MedMol) S81263-10mg 99% ¥350.00元 6 - - - EA 加入購(gòu)物車
源葉(MedMol) S81263-25mg 99% ¥690.00元 6 - - - EA 加入購(gòu)物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(COA)

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  • 提示:詳情請(qǐng)下載說明書。
  • 產(chǎn)品描述: RN486 is a potent, selective and orally active Btk inhibitor with an IC50 of 4.0 nM and a Kd of 0.31 nM. RN486 is less active for other kinases. RN486 can be used for rheumatoid arthritis and systemic lupus erythematosus research
  • 靶點(diǎn): IC50: 4.0 nM (Btk) Kd: 0.31 nM (Btk);BTK
  • 體外研究:
    RN486 blocks Fcε receptor cross-linking-induced degranulation in mast cells (IC50 = 2.9 nM), Fcγ receptor engagement-mediated tumor necrosis factor α production in monocytes (IC50 = 7 nM), and B cell antigen receptor-induced expression of an activation marker, CD69, in B cells in whole blood (IC50 = 21 nM). In a co-culture system consisting of human primary synovial FLS and activated human platelets, convulxin stimulation resulted in elevated production of pro-inflammatory cytokines, IL-6 and IL-8, an effect which is dose-dependently blocked by RN486
  • 體內(nèi)研究:
    RN486 produces robust anti-inflammatory and bone-protective effects in mouse CIA and rat adjuvant-induced arthritis (AIA) models. In the AIA model, RN486 (1-30 mg/kg) inhibits both joint and systemic inflammation, reducing both paw swelling and inflammatory markers in the blood
  • 參考文獻(xiàn):
    1. Xu D, et al. RN486, a selective Bruton's tyrosine kinase inhibitor, abrogates immune hypersensitivity responses and arthritis in rodents. J Pharmacol Exp Ther. 2012 Apr;341(1):90-103. 2. Hsu J, et al. Bruton's Tyrosine Kinase mediates platelet receptor-induced generation of microparticles: a potential mechanism for amplification of inflammatory responses in rheumatoid arthritis synovial joints. Immunol Lett. 2013 Feb;150(1-2):97-104. 3. Mina-Osorio P, et al. Suppression of glomerulonephritis in lupus-prone NZB × NZW mice by RN486, a selective inhibitor of Bruton's tyrosine kinase. Arthritis Rheum. 2013 Sep;65(9):2380-91.
  • 溶解性: soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.648 ml 8.241 ml 16.483 ml
    5 mM 0.33 ml 1.648 ml 3.297 ml
    10 mM 0.165 ml 0.824 ml 1.648 ml
    50 mM 0.033 ml 0.165 ml 0.33 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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