发明名称 Indolizino[3,2-c]quinoline derivatives, pharmaceutically acceptable salt thereof, preparation method thereof and pharmaceutical composition for treatment of cystic fibrosis containing the same as active ingredient
摘要 Provided are an indolizino[3,2-c]quinoline derivative, pharmaceutically acceptable salt thereof, and a method for preparing the same. The indolizino[3,2-c]quinoline derivative, pharmaceutically acceptable salt thereof may function as an agonist of cystic fibrosis conductance transmembrane regulator, and thus may be useful for an agent for preventing or treating diseases caused by degradation of activity of cystic fibrosis conductance transmembrane regulator and for a pharmaceutical composition for stimulating proliferation of stem cells.
申请公布号 US9296751(B1) 申请公布日期 2016.03.29
申请号 US201514884179 申请日期 2015.10.15
申请人 INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY 发明人 Kim Ikyon;Namkung Wan;Sung Jonghyuk
分类号 A61K31/4745;C07D471/06;C07D471/14 主分类号 A61K31/4745
代理机构 Duane Morris LLP 代理人 Duane Morris LLP ;Steele, Jr. J. Rodman;Lefkowitz Gregory M.
主权项 1. An indolizino[3,2-c]quinoline derivative represented by the following Chemical Formula 1 or pharmaceutically acceptable salt thereof: In Chemical Formula 1, R1, R2, R3, R4 and R5 are the same or different, and each independently represents H, F, Cl, Br, I, a C1-C6 alkyl, C1-C6 alkoxy, COOR7, aryl and a heteroaryl; R6 is selected from a C1-C6 alkyl, aryl and a heteroaryl; and R7 is H or a C1-C6 alkyl, wherein any 1-3 carbon atoms of the aryl and heteroaryl are linked to a substituent that is the same or different and is independently selected from H, F, Cl, Br, I, nitro, a C1-C6 alkyl and C1-C6 alkoxy.
地址 Seoul KR