Description
A BD2 bromodomain inhibitor (Kis = 4.6, 4.9, 1.6, and 1 nM for BRD2, -3, -4, and -T, respectively); selective for BD2 over BD1 bromodomains in a TR-FRET assay (Kis = 1,162, 3,140, 521, and 917 nM for BRD2, -3, -4, and -T, respectively); inhibits proliferation of SKM-1 leukemia cells (IC50 = 6.7 nM); induces cell cycle arrest at the G1 phase in LNCaP cells; reduces tumor volume in a SKM-1 mouse xenograft model at 18.8 mg/kg; reduces tumor growth in LNCaP and MDA PCa 2b mouse xenograft models at 1 and 4.7 mg/kg
Formal name: N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-1H-pyrrolo[2,3-c]pyridine-2-carboxamide
Synonyms:
Molecular weight: 491.6
CAS: 2138861-99-9
Purity: ≥98%
Formulation: A crystalline solid