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S88106

ZD-4190

源叶(MedMol) 98%
  • 英文名:
  • ZD-4190
  • 别名:
  • CAS号:
  • 413599-62-9
  • 分子式:
  • C19H16BrFN6O2
  • 分子量:
  • 459.2717432
  • 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) S88106-2mg 98% ¥1020.00元 5 - - - EA 加入购物车
源叶(MedMol) S88106-5mg 98% ¥1820.00元 6 - - - EA 加入购物车
源叶(MedMol) S88106-10mg 98% ¥2700.00元 6 - - - EA 加入购物车
源叶(MedMol) S88106-25mg 98% ¥4300.00元 6 - - - EA 加入购物车
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产品介绍

参考文献

质检证书(COA)

摩尔浓度计算器

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  • 产品描述: ZD-4190 is a potent, orally available inhibitor of the vascular endothelial cell growth factor receptor 2 (VEGFR2) and of epidermal growth factor receptor (EGFR) signalling, used for the treatment of cancer.
  • 靶点: EGFR; VEGFR2;EGFR; VEGFR
  • 体外研究:
    ZD4190 exhibits cytotoxic activity against the tumor cells
  • 体内研究:
    ZD4190 (100 mg/kg, p.o.) effectively delays MDA-MB-435 tumor growth in mice. In ZD4190-treated tumors, 18F-FPPRGD2 uptake has decreased significantly relative to baseline by 26.74±8.12% (p<0.05) on day 1 and by 41.19±6.63% (p<0.01) on day 3, then has returned to baseline on day 7. Tumor uptake of 18F-FLT has also decreased on both day 1 and day 3 after initiation of ZD4190 treatment. However, ZD4190 does not significantly change 18F-FDG uptake in tumors, compared with the control group. ZD4190 (50 mg/kg, p.o.) prevents outgrowth of residual tumour in a muscle model of minimal residual carcinoma. ZD4190 (12.5-100 mg/kg, p.o.) produces a dose-dependent reduction in K(trans) in PC-3 prostate tumors. At 100 mg/kg, ZD4190 reduces K(trans) in PC-3 tumors by 31% following 2 doses and by 53% following 8 doses
  • 参考文献:
    1. Yang M, et al. PET imaging of early response to the tyrosine kinase inhibitor ZD4190. Eur J Nucl Med Mol Imaging. 2011 Jul;38(7):1237-47. doi: 10.1007/s00259-011-1742-z. Epub 2011 Mar 1. 2. Gaballah K, et al. The antiangiogenic agent ZD4190 prevents tumour outgrowth in a model of minimal residual carcinoma in deep tissues. Br J Cancer. 2009 Aug 4;101(3):418-23. doi: 10.1038/sj.bjc.6605092. Epub 2009 Jul 21. 3. Checkley D, et al. Dynamic contrast-enhanced MRI of vascular changes induced by the VEGF-signalling inhibitor ZD4190 in human tumour xenografts. Magn Reson Imaging. 2003 Jun;21(5):475-82.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.177 ml 10.887 ml 21.774 ml
    5 mM 0.435 ml 2.177 ml 4.355 ml
    10 mM 0.218 ml 1.089 ml 2.177 ml
    50 mM 0.044 ml 0.218 ml 0.435 ml
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