| CPC A61K 31/519 (2013.01) [A61K 31/135 (2013.01); A61K 31/137 (2013.01); A61K 31/138 (2013.01); A61K 31/165 (2013.01); A61K 31/18 (2013.01); A61K 31/335 (2013.01); A61K 31/343 (2013.01); A61K 31/381 (2013.01); A61K 31/402 (2013.01); A61K 31/4155 (2013.01); A61K 31/416 (2013.01); A61K 31/4188 (2013.01); A61K 31/4245 (2013.01); A61K 31/426 (2013.01); A61K 31/427 (2013.01); A61K 31/428 (2013.01); A61K 31/4365 (2013.01); A61K 31/437 (2013.01); A61K 31/4409 (2013.01); A61K 31/4439 (2013.01); A61K 31/4525 (2013.01); A61K 31/454 (2013.01); A61K 31/47 (2013.01); A61K 31/496 (2013.01); A61K 31/502 (2013.01); A61K 31/517 (2013.01); A61K 31/5377 (2013.01); A61K 31/542 (2013.01); A61K 31/55 (2013.01); A61K 31/551 (2013.01); A61K 31/5513 (2013.01); A61P 25/24 (2018.01)] | 10 Claims |
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1. A method of treating a neurological disease or delaying of said neurological disease, wherein said neurological disease is depression or a subtype thereof in a subject in need thereof, said method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of Formula II:
![]() wherein:
RII′ is —H;
BII is optionally substituted cyclopentyl;
XII′ is —NR*—, or optionally substituted piperidinyl, piperazinyl, or pyrrolidinyl;
XII is an optionally substituted C1-C10 alkylenyl wherein optionally one or more carbon atoms are each independently replaced by —O—, or —NR*—;
YII is optionally substituted pyridyl, optionally substituted thiophenyl, optionally substituted furanyl, optionally substituted pyrazolyl, or optionally substituted phenyl; and
each R* is independently —H or optionally substituted C1-C6 alkyl;
and a pharmaceutically acceptable carrier, diluent or excipient thereof.
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