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LY-294,002盐酸盐

    
10mM in DMSO

LY-294,002 hydrochloride

源叶(MedMol)
V56810 一键复制产品信息
934389-88-5
C19H17NO3·HCl
343.80
2-(4-吗啉基)-8-苯基-4H-1-苯并吡喃-4-酮盐酸盐;LY-294,002 盐酸盐;2-morpholin-4-yl-8-phenylchromen-4-one,hydrochloride;LY-294,002 hydrochloride
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V56810-1ml
10mM in DMSO

¥580.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: 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.
靶点: PI3K
体内研究: 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
细胞实验: 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.
动物实验: 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.
参考文献: 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
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
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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参考文献

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摩尔浓度计算器

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