Disclosed is a compound of formula I, a stereoisomer thereof, a cis-trans-isomer thereof, a tautomer thereof, or a mixture thereof, or a pharmaceutically acceptable salt thereof, a solvate thereof or a prodrug thereof,
wherein R
1
, R
2
, R
3
and R
4
are each as defined in the present application.
[EN] HETEROARYLAMINOISOQUINOLINES, METHODS FOR THEIR PREPARATION AND THERAPEUTIC USES THEREOF<br/>[FR] HÉTÉROARYLAMINOISOQUINOLINES, PROCÉDÉS POUR LES PRÉPARER ET LEURS UTILISATIONS THÉRAPEUTIQUES
申请人:MINORYX THERAPEUTICS S L
公开号:WO2016120808A1
公开(公告)日:2016-08-04
The application is directed to compounds of formula (IA) : and specifically compounds of formula (I) and their salts and solvates, wherein R1, R11, R12, R13, R4, R5, n, A1, A2, and A3 are as set forth in the specification, as well as to a method for their preparation, pharmaceutical compositions comprising the same, and use thereof for the treatment and/or prevention of conditions associated with the alteration of the activity of β-galactosidase, specially galactosidase beta-1 or GLB1, including GM1 gangliosidoses and Morquio syndrome, type B.
POLYCYCLIC COMPOUND ACTING AS IDO INHIBITOR AND/OR IDO-HDAC DUAL INHIBITOR
申请人:Hangzhou Innogate Pharma Co., Ltd.
公开号:EP3686196A1
公开(公告)日:2020-07-29
The present invention provides polycyclic compounds as IDO inhibitors and/or dual inhibitors of IDO-HDAC. Specifically, the present invention provides compounds represented by the following formula (I), wherein each group is defined as described in the specification. The compounds have IDO inhibitory activity or IDO-HDAC dual inhibitory activity and can be used for preventing or treating diseases associated with IDO and/or IDO-HDAC activity or expression levels. At the same time, the compounds of the present invention can be combined with an antitumor antibody such as PD-1 and PD-L1, and such a combination can greatly increase the antitumor response rate of the antibody and broaden the types of tumors to be treated.
Disclosed is a compound of formula I, a stereoisomer thereof, a cis-trans-isomer thereof, a tautomer thereof, or a mixture thereof, or a pharmaceutically acceptable salt thereof, a solvate thereof or a prodrug thereof,
wherein R1, R2, R3 and R4 are each as defined in the present application.
公开了一种式 I 的化合物、其立体异构体、顺反异构体、同系物或其混合物,或其药学上可接受的盐、溶液或原药、
其中 R1、R2、R3 和 R4 各如本申请中所定义。