Development of N6-(Heteroarylcarbonyl)adenines as BRD4 Inhibitors
摘要:
N-6-(Heteroarylcarbonyl)adenines were synthesized as candidate BRD4 inhibitors, and their structure-activity relationships were investigated. Among the synthesized compounds, N-6-[(3-methoxythiophen-2-yl)carbonyl]adenine (15) showed the most potent BRD4-inhibitory activity.