ENMD-2076 L-(+)-Tartaric acid

    
98%

ENMD-2076 L-(+)-Tartaric acid

源叶(MedMol)
S80256 一键复制产品信息
1291074-87-7
C25H31N7O6
525.56
ENMD-2076 酒石酸盐
货号 规格 价格 上海 北京 武汉 南京 购买数量
S80256-5mg 98% ¥320.00 7 - - -
S80256-10mg 98% ¥578.00 6 - - -
S80256-50mg 98% ¥1300.00 2 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

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.

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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参考文献

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