| SKU | Size | Availability | Price | Qty |
|---|---|---|---|---|
| E655717-1ml | 1ml | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $139.90 |
| Specifications & Purity | 10mM in DMSO |
|---|---|
| Biochemical and Physiological Mechanisms | 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. |
| Storage Temp | Desiccated,Store at -80°C |
| Shipped In | Ice chest + Ice pads |
| Product Description | 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 ) |
| Canonical SMILES | CC1=CC(=NN1)NC2=CC(=NC(=N2)C=CC3=CC=CC=C3)N4CCN(CC4)C.C(C(C(=O)O)O)(C(=O)O)O |
|---|---|
| Molecular Weight | 525.56 |
Enter Lot Number to search for COA:
