4区 · 医学
Article
作者: Bursuker, Isia ; Webster, Kevin R. ; Kimball, S. David ; Shan, Weifang ; Mulheron, Janet G. ; Xiao, Hai-yun ; Kellar, Kristin A. ; Tokarski, John S. ; Sack, John S. ; Rawlins, David B. ; Misra, Raj N.
1H-Pyrazolo[3,4-b]pyridine 3 (SQ-67563) has been shown to be a potent, selective inhibitor of CDK1/CDK2 in vitro. In cells 3 acts as a cytotoxic agent with the ability to block cell cycle progression and/or induce apoptosis. The solid state structure of 3 bound to CDK2 shows 3 resides coincident with the ATP purine binding site and forms important H-bonding interactions with Leu83 on the protein backbone.