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S81367

EPZ011989

源葉(MedMol) 98%
  • 英文名:
  • EPZ011989
  • 別名:
  • N-[(1,2-Dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-3-[ethyl[trans-4-[(2-methoxyethyl)methylamino]cyclohexyl]amino]-2-methyl-5-[3-(4-morpholinyl)-1-propyn-1-yl]benzamide
  • CAS號(hào):
  • 1598383-40-4
  • 分子式:
  • C35H51N5O4
  • 分子量:
  • 605.8105
  • 核磁/質(zhì)譜:
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) S81367-5mg 98% ¥540.00元 8 - - - EA 加入購(gòu)物車
源葉(MedMol) S81367-10mg 98% ¥810.00元 5 - - - EA 加入購(gòu)物車
源葉(MedMol) S81367-50mg 98% ¥2550.00元 2 - - - 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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  • 產(chǎn)品描述: EPZ011989 is a potent and orally active Zeste Homolog 2 (EZH2) inhibitor with metabolic stability. EPZ011989 has inhibitory inhibition for EZH2 with a Ki value of <3 nM. EPZ011989 shows robust methyl mark inhibition and anti-tumor activity. EPZ011989 can be used for the research of various cancers
  • 靶點(diǎn): Ki: <3 nM (EZH2); IC50: 94 nM (H3K27 methylation inhibition);HistoneMethyltransferase
  • 體外研究:
    EPZ011989 inhibits mutant and wild-type EZH2 with an Ki value of <3 nM. EPZ011989 reduces cellular H3K27 methylation with an IC50 value of 94 nM. EPZ011989 (0-10 μM; 11 days) has anti-proliferation effect in WSU-DLCL2 cells. Cell Proliferation Assay Cell Line: WSU-DLCL2 cells Concentration: 0-10 μM Incubation Time: 11 days Result: Demonstrated an average lowest cytotoxic concentration (LCC) in WSU-DLCL2 cells of 208 nM.
  • 體內(nèi)研究:
    EPZ011989 (oral; 30-1000 mg/kg; single or bid; for 7 days or 21 days) can elicit robust methyl mark inhibition and antitumor activity. Animal Model: SCID mice Dosage: 125, 250, 500, and 1000 mg/kg Administration: Oral; single, twice-daily (BID)for 7 days or twice-daily (BID)for 21 days Result: Provided coverage over the LCC for 24 h (1000 mg/kg ), while the 250 and 500 mg/kg doses provided coverage over this value for approximately 8 h.Observed complete ablation of the methyl mark by the end of day 7.Showed robust tumor growth inhibition, methyl mark reduction and extended total and free plasma exposure time.
  • 參考文獻(xiàn):
    1. Campbell JE, et al. EPZ011989, A Potent, Orally-Available EZH2 Inhibitor with Robust in Vivo Activity. ACS Med Chem Lett. 2015 Mar 4;6(5):491-495.
  • 溶解性: soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.651 ml 8.253 ml 16.507 ml
    5 mM 0.33 ml 1.651 ml 3.301 ml
    10 mM 0.165 ml 0.825 ml 1.651 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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