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S80262

I-BET151

源葉(MedMol) 98%
  • 英文名:
  • I-BET151
  • 別名:
  • 7-(3,5-Dimethyl-1,2-Oxazol-4-Yl)-8-Methoxy-1-[(1r)-1-(Pyridin-2-Yl)ethyl]-1h,2h,3h-Imidazo[4,5-C]quinolin-2-One; 7-(3,5-Dimethyl-4-isoxazolyl)-1,3-dihydro-8-methoxy-1-[(1R)-1-(2-pyridinyl)ethyl]-2H-im
  • CAS號:
  • 1300031-49-5
  • 分子式:
  • C23H21N5O3
  • 分子量:
  • 415.44
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S80262-1mg 98% ¥130.00元 9 - - - EA 加入購物車
源葉(MedMol) S80262-2mg 98% ¥200.00元 8 - - - EA 加入購物車
源葉(MedMol) S80262-5mg 98% ¥450.00元 7 - - - EA 加入購物車
源葉(MedMol) S80262-10mg 98% ¥720.00元 6 - - - EA 加入購物車
源葉(MedMol) S80262-25mg 98% ¥1400.00元 5 - - - EA 加入購物車
源葉(MedMol) S80262-50mg 98% ¥2600.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S80262-100mg 98% ¥4400.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
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參考文獻(xiàn)

質(zhì)檢證書(COA)

摩爾濃度計算器

相關(guān)產(chǎn)品

  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: I-BET151 (GSK1210151A) is a BET bromodomain inhibitor which inhibits BRD4, BRD2, and BRD3 with pIC50 of 6.1, 6.3, and 6.6, respectively
  • 靶點: pIC50: 6.1 (BRD4), 6.3 (BRD2), 6.6 (BRD3)[1];EpigeneticReaderDomain
  • 體內(nèi)研究:
    I-BET151 demonstrates low blood clearance in the rat (~20% liver blood flow) and good oral systemic exposure which resulted in good oral bioavailability. High clearance is observed in the dog (~95% liver blood flow). The systemic exposure in the dog is low, resulting in a poor oral bioavailability of 16%. The high blood clearance in dog correlates well with the high intrinsic clearance observed in dog microsomes and hepatocytes, whereas the low intrinsic clearances seen in rat and mouse (mouse IVC 1.6 mL/min/g; CLb 8 mL/min/kg) correlate with lower in vivo blood clearances in these species. Due to the low systemic exposure observed in the dog, I-BET151 is investigated in the mini-pig as a potential second species for toxicological evaluation where it showed low clearance (~32% liver blood flow) and good bioavailability (65%). I-BET151 (30 mg/kg; i.p.; daily for 21 days)-treats mice has four- to five fold smaller myeloma tumors and a significantly reduces rate of tumor size doubling than vehicle-treated mice.
  • 參考文獻(xiàn):
    1. Seal J, et al. Identification of a novel series of BET family bromodomain inhibitors: Binding mode and profile of I-BET151 (GSK1210151A). Bioorg Med Chem Lett. 2012 Apr 15;22(8):2968-72. 2. Chaidos A, et al. Potent antimyeloma activity of the novel bromodomain inhibitors I-BET151 and I-BET762. Blood. 2014 Jan 30;123(5):697-705.
  • 溶解性: DMSO  :  ≥  100  mg/mL  (240.71  mM)
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.407 ml 12.035 ml 24.071 ml
    5 mM 0.481 ml 2.407 ml 4.814 ml
    10 mM 0.241 ml 1.204 ml 2.407 ml
    50 mM 0.048 ml 0.241 ml 0.481 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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