Il-17 modulators and uses thereof
OwnerYucheng PANG, Feiyang XU +1inventors
InventorsYucheng PANG, Feiyang XU, Xiangyang CHEN
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Abstract
The present invention relates to compounds suitable for inhibiting or regulating the activity of IL-17. The present invention is directed to compounds shown in Formula (I) and their pharmaceutically acceptable salts thereof. The present invention further relates to methods for treating and/or preventing various human diseases, including inflammatory and autoimmune disorders. The present invention also provides methods for preparing the compounds of the present invention.
Claims7
A compound according to Formula (IIb),
- or a pharmaceutically acceptable salt thereof,
- wherein:
- B is C1-6 alkyl or C3-10 cycloalkyl, where one or more hydrogens of the alkyl and cycloalkyl are optionally substituted by C3-10 cycloalkyl, C1-6 alkyl, C1-2 alkenyl or halogen, where one or more hydrogens of the alkyl, cycloalkyl and alkenyl are further optionally substituted by halogen or C1-6 alkyl;
- X is CH or N;
- Y1 is N or CR31;
- Y2 is N, NR32 or CR31;
- Y3 is N, NR32, O or S;
- R31 is H, halogen or C1-6 alkyl;
- R32 is C1-6 alkyl, C3-6 cycloalkyl or 4- to 6-membered heterocyclyl, where one or more hydrogens of the alkyl, cycloalkyl and heterocyclyl are optionally substituted by C3-6 cycloalkyl, halogen, C1-6 alkyl, 4- to 6-membered heterocyclyl, —ORb or —NR13R14, where one or more hydrogens of cycloalkyl and heterocyclyl are further optionally substituted by halogen or C1-6 alkyl;
- R1 is C1-6 alkyl, where one or more hydrogens of the alkyl are optionally substituted by halogen, D, CN, 4- to 6-membered heterocyclyl, —ORd or —NR15R16.
- R2 is methyl or cyclopropyl;
- R3 is H, F or —OCH3;
- R6 is 5-membered heteroaryl containing one to three heteroatoms selected from N, O and S, where one or more hydrogens of the heteroaryl are optionally substituted by C1-6 alkyl, fluorinated C1-6 alkyl, deuterated C1-6 alkyl or C3-6 cycloalkyl;
- Rd is H, C1-6 alkyl, C3-6 cycloalkyl or 4- to 6-membered heterocyclyl, where one or more hydrogens of the alkyl, cycloalkyl and heterocyclyl are optionally substituted by F, D, C1-6 alkyl or C3-6 cycloalkyl;
- and
- Rb, R13, R14, R15 and R16 are independently selected from H, C1-6 alkyl and C3-6 cycloalkyl.
A compound having the following structure:
- or a pharmaceutically acceptable salt, or a stable isotope derivative thereof, or a stereoisomer thereof.
A compound having the following structure:
- or a pharmaceutically acceptable salt, or a stable isotope derivative thereof, or a stereoisomer thereof.
A compound having the following structure:
- or a pharmaceutically acceptable salt, or a stable isotope derivative thereof, or a stereoisomer thereof.
Dependencies are inferred from the claim text.