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S88228

LY-294,002 hydrochloride

源葉(MedMol) 98% (HPLC)
  • 英文名:
  • LY-294,002 hydrochloride
  • 別名:
  • 2-(4-嗎啉基)-8-苯基-4H-1-苯并吡喃-4-酮鹽酸鹽;LY-294,002 鹽酸鹽;2-morpholin-4-yl-8-phenylchromen-4-one,hydrochloride
  • CAS號(hào):
  • 934389-88-5
  • 分子式:
  • C19H17NO3·HCl
  • 分子量:
  • 343.80
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) S88228-5mg 98% (HPLC) ¥705.00元 5 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S88228-10mg 98% (HPLC) ¥815.00元 4 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S88228-25mg 98% (HPLC) ¥1455.00元 4 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S88228-50mg 98% (HPLC) ¥2428.00元 2 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S88228-100mg 98% (HPLC) ¥3818.00元 4 - - - EA 加入購(gòu)物車(chē)
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相關(guān)產(chǎn)品

  • 產(chǎn)品描述: LY294002 is a synthetic molecule inhibitor of PI3Kα/δ/β (IC50: 0.5/0.57/0.97 μM, in cell-free assays); more stable than Wortmannin in solution, and also is a blocker of autophagosome formation.
  • 靶點(diǎn): PI3K
  • 體內(nèi)研究:
    LY294002 can suppress tumor growth and induce apoptosis, especially in the LoVo tumors. Thus, It shows remarkable effectiveness in the mouse peritonitis carcinoma tosa model. LY294002 markedly inhibits growth and ascites formation of ovarian carcinoma
  • 細(xì)胞實(shí)驗(yàn): Cell lines: Colon cancer cell lines DLD-1,LoVo,HCT15,and Colo205. Concentrations: 0–50 μM. Incubation Time: 0–48 hours. Method: 1.0×105 cells (100 μL volume/well) are inoculated into 96-well microtiter plates.LY294002 is added to triplicate wells and cultured at 37oC for 0–48 hours.After treatment,Premix WST-1 (10 μL) is added to each microculture well,and the plates are incubated for 60 minutes at 37oC,after which absorbance at 450 nm is measured with a microplate reader.
  • 動(dòng)物實(shí)驗(yàn): Animal Models: Two groups of athymic nude mice (5–7 weeks) are inoculated i.p.with OVCAR-3 cells. Formulation: Dissolved in DMSO plus 0.25 ml of PBS. Dosages: 0–100 mg/kg. Administration: i.p.
  • 參考文獻(xiàn):
    1. Hu L, et al. In vivo and in vitro ovarian carcinoma growth inhibition by a phosphatidylinositol 3-kinase inhibitor (LY2942002). Clin Cancer Res. 2000 Mar;6(3):880-6. 2. Semba S, et al. The in vitro and in vivo effects of 2-(4-morpholinyl)-8-phenyl-chromone (LY2942002), a specific inhibitor of phosphatidylinositol 3'-kinase, in human colon cancer cells. Clin Cancer Res. 2002 Jun;8(6):1957-63. 3. Chaussade C, et al. Evidence for functional redundancy of class IA PI3K isoforms in insulin signalling. Biochem J. 2007 Jun 15;404(3):449-58. 4. Gharbi SI, et al. Exploring the specificity of the PI3K family inhibitor LY2942002. Biochem J. 2007 May 15;404(1):15-21.
  • 溶解性: Soluble  in  DMSO、Ethanol
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.909 ml 14.543 ml 29.087 ml
    5 mM 0.582 ml 2.909 ml 5.817 ml
    10 mM 0.291 ml 1.454 ml 2.909 ml
    50 mM 0.058 ml 0.291 ml 0.582 ml
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