CPC C07D 491/048 (2013.01) [A61K 31/415 (2013.01); A61K 31/4164 (2013.01); A61K 31/421 (2013.01); A61K 31/4245 (2013.01); C07C 235/22 (2013.01); C07D 207/27 (2013.01); C07D 233/36 (2013.01); C07D 233/42 (2013.01); C07D 233/61 (2013.01); C07D 233/64 (2013.01); C07D 249/04 (2013.01); C07D 249/08 (2013.01); C07D 257/04 (2013.01); C07D 261/04 (2013.01); C07D 261/08 (2013.01); C07D 263/32 (2013.01); C07D 263/38 (2013.01); C07D 263/56 (2013.01); C07D 271/06 (2013.01); C07D 271/10 (2013.01); C07D 291/04 (2013.01); C07D 401/12 (2013.01); C07D 403/04 (2013.01); C07D 403/12 (2013.01); C07D 413/04 (2013.01); C07D 413/06 (2013.01); C07D 413/12 (2013.01); C07D 417/04 (2013.01); C07D 471/04 (2013.01); C07D 487/04 (2013.01)] | 18 Claims |
1. A method for treating a disease or condition mediated, at least in part, by eukaryotic initiation factor 2B, the method comprising administering to a subject in need thereof an effective amount of a compound, or a pharmaceutically acceptable salt, isotopically enriched analog, stereoisomer, mixture of stereoisomers, or prodrug thereof, selected from the group consisting of:
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