计算溶液所需的质量、体积或浓度。
为什么选择此级别
，适用于对基线干扰要求严格的色谱和分析工作流程。
储存与运输
干燥,-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。
质量文档
SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。
文献证明
在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
概述
ENMD-2076 Tartrate is a multi-targeted kinase inhibitor with IC 50 s 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.
In Vitro
ENMD-2076 is selective toward Aurora A versus Aurora B (IC 50 =350 nM). ENMD-2076 inhibits HUVEC growth with an IC 50 value of 0.15 mM. Against 10 human leukemia cell lines, the IC 50 values range from 0.025 to 0.53 mM. Within this panel, MV4:11 cells are the most sensitive cells by a factor of greater than 4. The lymphoma-derived U937 cell line treated with ENMD-2076 shows that the ENMD-2076 induces a dose-dependent increase in G2-M-phase arrest as well as the induction of apoptosis. ENMD-2076 inhibits cellular Flt3 ligand (FL)-induced Flt3 autophosphorylation in THP-1 cells, which have been shown to express FL-responsive wild-type Flt- 3 (18) with an IC 50 value of 28 nM. ENMD-2076 inhibits stem cell factor (SCF)-induced Kit autophosphorylation in MO7e cells with an IC 50 value of 40 nM. ENMD-2076 inhibits VEGFR2/KDR autophosphorylation with an IC 50 value of 7 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
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 . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
IC50& Target:Aurora A 1.86 nM (IC 50 ) KDR 58.2 nM (IC 50 ) Flt-4 15.9 nM (IC 50 ) FGFR1 92.7 nM (IC 50 ) FGFR2 70.8 nM (IC 50 ) PDGFRα 56.4 nM (IC 50 ) Flt3 14 nM (IC 50 )
规格
别名
ENMD-2076 酒石酸盐
规格或纯度
10mM in DMSO
英文名称
ENMD-2076 Tartrate
生化机理
ENMD-2076 酒石酸盐是一种多靶点激酶抑制剂，对 Aurora A , Flt3 , KDR/VEGFR2 , Flt4/VEGFR3 , FGFR1 , FGFR2 , Src , PDGFRα 的 IC 50 s 分别为 1.86、14、58.2、15.9、92.7、70.8、56.4 nM。
储存条件
干燥,-80℃储存
运输条件
特低温运输
名称和识别符
分子类型
小分子
Isomeric SMILES
CC1=CC(=NN1)NC2=CC(=NC(=N2)/C=C/C3=CC=CC=C3)N4CCN(CC4)C.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O
关联CAS
PubChem CID
分子量
525.56
技术文档
高级数据
安全和危险性（GHS）
质检证书（CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:
溶液计算器
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