发明名称 |
Imidazole-1-yl pyrimidine derivatives, or pharmacutically acceptable salt thereof, and pharmaceutic composition comprising the same as an active ingredient |
摘要 |
The present invention relates to a novel imidazole-1-yl pyrimidine derivative, a pharmaceutically acceptable salt thereof, and a pharmaceutic composition comprising the same. Since the imidazole-1-yl pyrimidine derivative according to the present invention shows the inhibition activity selectively to BRAF, BRAF mutants, or CRAF, it can be used to a pharmaceutic composition for preventing or treating cancer. |
申请公布号 |
US9540348(B2) |
申请公布日期 |
2017.01.10 |
申请号 |
US201514713037 |
申请日期 |
2015.05.15 |
申请人 |
INDUSTRYUNIVERSITY COOPERATION FOUNDATION HANYANG UNIVERSITY ERICA CAMPUS |
发明人 |
Hah Jung-Mi |
分类号 |
B65D25/20;B65D83/00;C07D403/04;C07D403/14;C07D401/14;C07D405/14 |
主分类号 |
B65D25/20 |
代理机构 |
Lex IP Meister, PLLC |
代理人 |
Lex IP Meister, PLLC |
主权项 |
1. An imidazole-1-yl pyrimidine derivative represented by the following Chemical Formula 1, or a pharmaceutically acceptable salt thereof: in Chemical Formula 1, Q1 is —CH2— or —CO—; Q2 is —CO— or —CONH—; R1 is a C6-C20 aryl, a C7-C20 alkylaryl, a C7-C20 arylalkyl, a C5-C20 heteroaryl, a C3-C20 cycloalkyl, or a C3-C20 heterocycloalkyl, wherein said R1 is substituted with a halogen, a halogenated alkyl, hydroxyl group, carbonyl group, cyano group, alkoxy group, or a C3-C20 heterocycloalkyl or not. |
地址 |
Ansansi KR |