Compounds, compositions, and methods
AssigneeDenali Therapeutics Inc.
InventorsAnthony A. Estrada, Jianwen A. Feng, Joseph P. Lyssikatos, Zachary K. Sweeney, Javier de Vicente Fidalgo
Life of this patent
Estimating the term…
Abstract
The present disclosure relates generally to LRRK2 inhibitors, or a pharmaceutically acceptable salt, deuterated analog, prodrug, tautomer, stereoisomer, or mixture of stereoisomers thereof, and methods of making and using thereof.
Claims32
A compound of formula I:
- or a pharmaceutically acceptable salt, deuterated analog, prodrug, stereoisomer, or a mixture of stereoisomers thereof, wherein:
- R1 is optionally substituted cycloalkyl or, when R5 is —CR5aR6R7 where R5a is optionally substituted triazol-2-yl, R1 is optionally substituted cycloalkyl or C1-6 alkyl optionally substituted with halo;
- R2 is halo, cyano, optionally substituted C1-6 alkyl, optionally substituted C1-6 alkenyl, optionally substituted C1-6 alkynyl, optionally substituted cycloalkyl, optionally substituted C1-6 alkoxy, optionally substituted cycloalkoxy, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkylsulfonyl, —C(O)R10, or —C(O)N(R11)(R12);
- R3 is optionally substituted C1-6 alkoxy, optionally substituted cycloalkyl, optionally substituted cycloalkoxy, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkylsulfonyl, or
- —N(R11)(R12);
- R4 is hydrogen or halo;
- R5 is hydrogen, halo, cyano, optionally substituted C1-6 alkyl, optionally substituted C1-6 alkenyl, optionally substituted C1-6 alkynyl, optionally substituted cycloalkyl, optionally substituted heterocyclyl, optionally substituted heteroaryl, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkyl sulfonyl, —C(O)R10, or —C(O)N(R11)(R12);
- each R10 is independently optionally substituted C1-6 alkyl or optionally substituted C1-6 alkoxy;
- and
- R11 and R12 are each independently hydrogen, optionally substituted C1-6 alkyl, or optionally substituted cycloalkyl.
A compound of Table 1A, Table 1B, Table 2A or Table 2B, or a pharmaceutically acceptable salt, deuterated analog, prodrug, tautomer, stereoisomer, or a mixture of stereoisomers thereof.
A pharmaceutical composition comprising a compound of Table 1A, Table 1B, Table 2A or Table 2B, or a pharmaceutically acceptable salt, deuterated analog, prodrug, tautomer, stereoisomer, or a mixture of stereoisomers thereof, and a pharmaceutically acceptable carrier, diluent, or excipient.
-36. (canceled)
Dependencies are inferred from the claim text.