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S84088

(E)-3PO

源叶(MedMol) 99%
  • 英文名:
  • 3-(3-Pyridinyl)-1-(4-pyridinyl)-2-propen-1-one
  • 别名:
  • (E)-3-Pyridin-3-yl-1-pyridin-4-yl-propenone;3PO
  • CAS号:
  • 18550-98-6
  • 分子式:
  • C13H10N2O
  • 分子量:
  • 210.2313
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S84088-5mg 99% ¥480.00元 6 - - - EA 加入购物车
源叶(MedMol) S84088-10mg 99% ¥690.00元 8 - - - EA 加入购物车
源叶(MedMol) S84088-25mg 99% ¥1270.00元 3 - - - EA 加入购物车
源叶(MedMol) S84088-50mg 99% ¥2050.00元 5 - - - EA 加入购物车
源叶(MedMol) S84088-100mg 99% ¥3100.00元 5 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: 3PO is a small-molecule inhibitor of PFKFB3 (IC50: 22.9 μM), inhibiting the proliferation of several human malignant hematopoietic and adenocarcinoma cell lines (IC50: 1.4-24 μM). It suppresses glucose uptake, and decreases the intracellular concentration of Fru-2,6-BP, lactate, ATP, NAD+, and NADH.
  • 靶点: Autophagy;Glucokinase;Glucokinase; Autophagy
  • 体外研究:
    3PO markedly attenuates the proliferation of several human malignant hematopoietic and adenocarcinoma cell lines (IC50, 1.4-24 μM) and is selectively cytostatic to ras-transformed human bronchial epithelial cells relative to normal human bronchial epithelial cells. Compared with the wild-type PFKFB3+/+transformed cells (IC50, 49 μM), the PFKFB3+/- fibroblasts were more sensitive to compound 3PO treatment (IC50, 26 μM). 3PO Causes G2-M phase arrest, which Is preceded by decreased Fru-2,6-BP and glucose uptake. 3PO slows growth through inhibition of PFK-2 activity, then ectopic expression of the PFKFB3 isozyme may thwart the cytostatic activity of 3PO. 3PO inhibits the glycolytic regulator PFKFB3 in endothelial cells (ECs). 3PO decreases glycolysis in ECs and impairs vessel sprouting. 3PO also suppresses vascular hyperbranching induced by inhibition of Notch or VEGF receptor 1 (VEGFR1) and amplified the antiangiogenic effect of VEGF blockade.
  • 体内研究:
    Compared with vehicle control, compound 3PO treatment significantly reduced Fru-2,6-BP in tumor xenografts (vehicle: 13.1 ± 1.9 pmol/mg, 3PO: 8.5 ± 1.7 pmol/mg). 3PO also impairs (pathological) angiogenesis.
  • 参考文献:
    1. Clem B, et al. Small-molecule inhibition of 6-phosphofructo-2-kinase activity suppresses glycolytic flux and tumor growth. Mol Cancer Ther. 2008 Jan;7(1):110-20. 2. Schoors S, et al. Partial and transient reduction of glycolysis by PFKFB3 blockade reduces pathological angiogenesis. Cell Metab. 2014 Jan 7;19(1):37-48. 3. Lea MA, Inhibition of Growth of Bladder Cancer Cells by 3-(3-Pyridinyl)-1-(4-pyridinyl)-2-propen-1-one in Combination with Other Compounds Affecting Glucose Metabolism. Anticancer Res. 2015 Nov;35(11):5889-99.
  • 溶解性: Soluble  in  DMSO、Ethanol
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 4.757 ml 23.783 ml 47.567 ml
    5 mM 0.951 ml 4.757 ml 9.513 ml
    10 mM 0.476 ml 2.378 ml 4.757 ml
    50 mM 0.095 ml 0.476 ml 0.951 ml
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