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ENMD-2076
Cat. No.:
OB0225WX-2398
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
Add to basket
Product Overview
Description:
ENMD-2076 is a selective kinase inhibitor targeting Aurora A (IC50: 14 nM) and Flt3 (IC50: 1.86 nM), showing 25-fold higher selectivity for Aurora A over Aurora B.
Synonym:
934353-76-1; ENMD 2076; (E)-N-(5-Methyl-1H-pyrazol-3-yl)-6-(4-methylpiperazin-1-yl)-2-styrylpyrimidin-4-amine; Enmd-2076 free base; 6-(4-methylpiperazin-1-yl)-N-(5-methyl-1H-pyrazol-3-yl)-2-[(E)-2-phenylethenyl]pyrimidin-4-amine; R-440; 4-Pyrimidinamine, 6-(4-methyl-1-piperazinyl)-N-(5-methyl-1H-pyrazol-3-yl)-2-((1E)-2-phenylethenyl)-; (E)-N-(5-methyl-1H-pyrazol-3-yl)-6-(4-methylpiperazin-1-yl)-2-styrylpyrimidin-4-amine.; 4-Pyrimidinamine, 6-(4-methyl-1-piperazinyl)-N-(5-methyl-1H-pyrazol-3-yl)-2-[(1Z)-2-phenylethenyl]-; 6-(4-methylpiperazin-1-yl)-N-(5-methyl-1H-pyrazol-3-yl)-2-((E)-2-phenylethenyl)pyrimidin-4-amine; N-(5-methyl-1H-pyrazol-3-yl)-6-(4-methylpiperazin-1-yl)-2-styrylpyrimidin-4-amine; 6-(4-Methyl-1-piperazinyl)-N-(5-methyl-1H-pyrazol-3-yl)-2-[(E)-2-phenylethenyl]-4-pyrimidinamine
CAS No.:
934353-76-1
Compound CID:
16041424
Formula:
C21H25N7
Formula Weight:
375.47
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
ENMD-2076 is applied in oncology research as a multi-target kinase inhibitor with high affinity for Aurora A and VEGFR2 to investigate the regulation of mitosis and the suppression of tumor vascular signaling.
Library Information
Target:
Aurora kinase; CSF-1R; FGFR; FLT3; PDGFR; Src; VEGFR
Receptor:
Aurora kinase; CSF-1R; FGFR; FLT3; PDGFR; Src; VEGFR
Pathways:
Angiogenesis
Plate Number:
L6700-01
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
105 mg/mL; 279.65 mM
Water Max Solubility:
1 mg/mL; 2.66 mM
ALogP:
4.015
HBA_Count:
3
HBD_Count:
2
Rotatable Bond:
5





