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Smiles: N#CC1=CC(=CC=C1OC1CCOCC1)C1=NC(NC2C=CC(=CC=2)N2CCN(CC2)C2COC2)=NC=N1
(2002) Blood
6R)-2-{[(2S)-2-[(1S
EXP3174 inhibits the angiotensin II-induced cell protein synthesis with an IC50 of 3 nM
InChi: InChI=1S/C20H16Br2N2O3S/c21-16-7-9-17(10-8-16)24-20(25)15-6-11-18(22)19(12-15)28(26
ENMD-2076 ohesperidin dihydrochalcone Smiles: N#CC1=CC(=CC=C1OC1CCOCC1)C1=NC(NC2C=CC(=CC=2)N2CCN(CC2)C2COC2)=NC=N1ENMD 2076 is an orally active, Aurora A angiogenic kinase inhibitor with a unique kinase selectivity profile and multiple mechanisms of action. ENMD 2076 has been shown to inhibit a distinct profile of angiogenic tyrosine kinase targets in addition to the Aurora A kinase. Aurora kinases are key regulators of mitosis (cell division), and are often over expressed in human cancers. ENMD 2076 also targets the VEGFR, Flt 3 and FGFR3 kinases which have been