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S80829

LY2090314

源葉(MedMol) 99%
  • 英文名:
  • LY2090314
  • 別名:
  • LY2090314; LY-2090314; LY 2090314;3-(9-fluoro-2-(piperidine-1-carbonyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-7-yl)-4-(imidazo[1,2-a]pyridin-3-yl)-1H-p
  • CAS號(hào):
  • 603288-22-8
  • 分子式:
  • C28H25FN6O3
  • 分子量:
  • 512.53
  • 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(chē)...
源葉(MedMol) S80829-5mg 99% ¥560.00元 3 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S80829-10mg 99% ¥800.00元 6 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S80829-25mg 99% ¥1020.00元 5 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S80829-100mg 99% ¥2750.00元 預(yù)計(jì)交期:2-3天 - - - EA 加入購(gòu)物車(chē)
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  • 提示:詳情請(qǐng)下載說(shuō)明書(shū)。
  • 產(chǎn)品描述: LY2090314 is a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 values of 1.5 nM and 0.9 nM for GSK-3α and GSK-3β, respectively.
  • 靶點(diǎn): GSK-3β:0.9 nM (IC50);GSK-3α;1.5 nM (IC50);GSK-3
  • 體外研究:
    LY2090314 (20 nM) promotes a time-dependent stabilization of β-catenin total protein as well as an induction of Axin2. LY2090314 is highly selective towards GSK3 as demonstrated by its fold selectivity relative to a large panel of kinases. LY2090314 potently induces apoptotic cell death in a panel of melanoma cell lines irrespective of BRAF mutation status. Cell death induced by LY2090314 is dependent on β-catenin and GSK3β knockdown increases the sensitivity of cells to LY2090314. LY2090314 remains active in cell lines resistant to PLX4032 and has an independent mechanism of action.
  • 體內(nèi)研究:
    LY2090314 exhibits high clearance (approximating hepatic blood flow) and a moderate volume of distribution (appr 1-2 L/kg) resulting in rapid elimination (half-life appr 0.4, 0.7, and 1.8-3.4 hours in rats, dogs, and humans, respectively). LY2090314 is rapidly cleared by extensive metabolism with negligible circulating metabolite exposures due to biliary excretion of metabolites into feces with no apparent intestinal reabsorption. LY2090314 (25 mg/kg Q3D, i.v.) elevates Axin2 gene expression in vivo, demonstrates single agent activity in the A375 xenograft model of melanoma and enhances the efficacy of DTIC.
  • 參考文獻(xiàn):
    1. Zamek-Gliszczynski MJ, et al. Pharmacokinetics, metabolism, and excretion of the glycogen synthase kinase-3 inhibitor LY2090314 in rats, dogs, and humans: a case study in rapid clearance by extensive metabolism with low circulating metabolite exposure. Dr
    2. Atkinson JM, et al. Activating the Wnt/β-Catenin Pathway for the Treatment of Melanoma--Application of LY2090314, a Novel Selective Inhibitor of Glycogen Synthase Kinase-3. PLoS One. 2015 Apr 27;10(4):e0125028.
  • 溶解性: soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.951 ml 9.756 ml 19.511 ml
    5 mM 0.39 ml 1.951 ml 3.902 ml
    10 mM 0.195 ml 0.976 ml 1.951 ml
    50 mM 0.039 ml 0.195 ml 0.39 ml
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