Structure of Human ROS1 Kinase Domain in Complex with PF-06463922
收藏Protein Data Bank Japan2024-01-10 更新2026-03-21 收录
下载链接:
https://pdbj.org/mine/summary/4uxl
下载链接
链接失效反馈官方服务:
资源简介:
Structure of Human ROS1 Kinase Domain in Complex with PF-06463922 Descriptor: (10R)-7-amino-12-fluoro-2,10,16-trimethyl-15-oxo-10,15,16,17-tetrahydro-2H-8,4-(metheno)pyrazolo[4,3-h][2,5,11]benzoxadiazacyclotetradecine-3-carbonitrile, PROTO-ONCOGENE TYROSINE-PROTEIN KINASE ROS Authors: McTigue, M, Deng, Y, Liu, W, Brooun, A, Stewart, A. Deposit date: 2014-08-25 Release date: 2015-03-11 Last modified: 2024-01-10 Method: X-RAY DIFFRACTION (2.4 Å) Cite: Pf-06463922 is a Potent and Selective Next-Generation Ros1/Alk Inhibitor Capable of Blocking Crizotinib-Resistant Ros1 Mutations. Proc.Natl.Acad.Sci.USA, 112, 2015
人类ROS1激酶域与PF-06463922复合物的结构 描述:(10R)-7-氨基-12-氟-2,10,16-三甲基-15-氧代-10,15,16,17-四氢-2H-8,4-(亚甲基)吡唑并[4,3-h][2,5,11]苯并氧杂十四氮杂环辛四烯-3-甲腈;原癌基因酪氨酸蛋白激酶ROS(Proto-Oncogene Tyrosine-Protein Kinase ROS)
作者:McTigue, M、Deng, Y、Liu, W、Brooun, A、Stewart, A
提交日期:2014-08-25
发布日期:2015-03-11
最后修改日期:2024-01-10
实验方法:X射线衍射(分辨率2.4 Å)
引用文献:PF-06463922是一种强效且高选择性的新一代Ros1/Alk抑制剂,可阻断克唑替尼耐药性Ros1突变。《美国国家科学院院刊》(Proc.Natl.Acad.Sci.USA),112卷,2015年
创建时间:
2014-08-25



