PF
CAS NO.
英文品名 PF
中文品名 PF
分子式 C21H19FN6O2
分子量 406.15
规格/纯度 98%
供应能力 can supply g scale
别名 PF ;PF
产品简述 PF is a novel, orally available, CNS-penetrant, ATP-competitive inhibitor of ALK/ROS1 with Ki of <0.02 nM, <0.07 nM, and 0.7 nM for ROS1, ALK (WT), and ALK (L1196M), respectively.
详细说明 PF demonstrates significant cell activity against ALK and a large set of ALK clinical mutations with IC50 ranging from 0.2 nM-77 nM. PF exhibited subnanomolar cellular potency against oncogenic ROS1 fusions and inhibited the crizotinib-refractory ROS1(G2032R) mutation and the ROS1(G2026M) gatekeeper mutation. Compared with crizotinib and the second-generation ALK/ROS1 inhibitors ceritinib and alectinib, PF showed significantly improved inhibitory activity against ROS1 kinase. in vivo: PF showed marked antitumor activity in tumor models expressing FIG-ROS1, CD74-ROS1, and the CD74-ROS1(G2032R) mutation. Furthermore, PF demonstrated antitumor activity in a genetically engineered mouse model of FIG-ROS1 glioblastoma.
