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公开(公告)号:US20210078972A1
公开(公告)日:2021-03-18
申请号:US17044322
申请日:2019-03-29
Applicant: HAIHE BIOPHARMA CO., LTD. , JINAN UNIVERSITY , SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES
Inventor: Ke DING , Meiyu GENG , Shingpan CHAN , Jian DING , Li TAN , Jing AI , Zhang ZHANG , Xia PENG , Xiaomei REN , Yinchun JI , Zhengchao TU , Yang DAI , Xiaoyun LU
IPC: C07D401/12 , A61P35/00
Abstract: The present invention relates to quinoline or quinazoline compound represented by the formula (I), a pharmaceutically acceptable salt thereof, a stereoisomer thereof, a prodrug molecule thereof, or a deuterated compound thereof. The compound of the present invention is effective in inhibiting the action of AXL protein kinase and can inhibit proliferation, migration, and invasion of various tumor cells. Further, the quinoline or quinazoline compound of the present invention has excellent metabolic stability, high in vivo antitumor activity, low toxic side effects, and can be used for preparing a drug for preventing hyperproliferative diseases such as tumors in humans and other mammals.
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公开(公告)号:US20220324869A1
公开(公告)日:2022-10-13
申请号:US17640424
申请日:2020-09-03
Inventor: Wenhu DUAN , Meiyu GENG , Hefeng ZHANG , Jian DING , Jing AI , Xia PENG , Yinchun JI
IPC: C07D487/04 , A61P35/00 , C07D401/14 , C07D405/14 , C07F7/08
Abstract: A compound having Axl and c-Met kinase inhibitory activity, a preparation method therefor and an application thereof are provided. Specifically, provided herein are a compound having the structure represented by formula (I), a preparation method therefor and an application thereof in the preparation of a medication for the treatment and/or prevention of tumor-associated diseases and/or kinase-related diseases.
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公开(公告)号:US20210221807A1
公开(公告)日:2021-07-22
申请号:US17057199
申请日:2019-05-21
Inventor: Hong LIU , Meiyu GENG , Yu ZHOU , Jian DING , Feifei FANG , Jing AI , Jian LI , Xia PENG , Hualiang JIANG , Yinchun JI , Kaixian CHEN
IPC: C07D471/04 , C07D519/00
Abstract: Provided are a class of fused-cyclic pyrazolone formamide compounds and a preparation method therefor, a pharmaceutical composition and the use thereof. Specifically, provided is a compound having the structure as shown in formula (I) (with each group defined in the description). The compound can be used as an AXL inhibitor in the preparation of a pharmaceutical composition for treating tumors.
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