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S80256

ENMD-2076 L-(+)-Tartaric acid

源叶(MedMol) 98%
  • 英文名:
  • ENMD-2076 L-(+)-Tartaric acid
  • 别名:
  • ENMD-2076 酒石酸盐
  • CAS号:
  • 1291074-87-7
  • 分子式:
  • C25H31N7O6
  • 分子量:
  • 525.56
  • 核磁/质谱:
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源叶(MedMol) S80256-5mg 98% ¥320.00元 7 - - - EA 加入购物车
源叶(MedMol) S80256-10mg 98% ¥578.00元 6 - - - EA 加入购物车
源叶(MedMol) S80256-50mg 98% ¥935.00元 2 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: ENMD-2076 Tartrate is a multi-targeted kinase inhibitor with IC50s of 1.86, 14, 58.2, 15.9, 92.7, 70.8, 56.4 nM for Aurora A, Flt3, KDR/VEGFR2, Flt4/VEGFR3, FGFR1, FGFR2, Src, PDGFRα, respectively.
  • 靶点: Aurora A:1.86 nM (IC50);KDR:58.2 nM (IC50);Flt-4:15.9 nM (IC50);FGFR1:92.7 nM (IC50);FGFR2:70.8 nM (IC50);PDGFRα:56.4 nM (IC50);Flt3:14 nM (IC50)
  • 体内研究:
    ENMD-2076 treatment results in statistically significant, dose dependent inhibition of tumor growth or tumor regression. Moreover, there is no correlation between tumor growth rate and antitumor efficacy, which would conceivably be expected for a mitotic kinase inhibitor, as fast growing (e.g., A375 melanoma) and slow-growing (e.g., HT29 colon carcinoma) tumors are similarly inhibited by ENMD-2076. ENMD-2076 is well tolerated at daily doses up to 302 mg/kg (equivalent to 200 mg/kg of the free base), with no weight loss or signs of morbidity noted in any study at this dose with the exception of the A375 model
  • 参考文献:
    1. Fletcher GC, et al. ENMD-2076 is an orally active kinase inhibitor with antiangiogenic and antiproliferative mechanisms of action. Mol Cancer Ther. 2011 Jan;10(1):126-37. 2. Wang X, et al. Preclinical activity of a novel multiple tyrosine kinase and aurora kinase inhibitor, ENMD-2076, against multiple myeloma. Br J Haematol. 2010 Aug;150(3):313-25.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 1.903 ml 9.514 ml 19.027 ml
    5 mM 0.381 ml 1.903 ml 3.805 ml
    10 mM 0.19 ml 0.951 ml 1.903 ml
    50 mM 0.038 ml 0.19 ml 0.381 ml
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