US2012238584A1PendingUtilityA1
5-HT1A receptor subtype agonist
Est. expiryJan 29, 2021(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/16A61P 25/00A61P 25/18A61P 25/24A61P 25/28A61P 25/06A61P 3/04A61K 45/06A61K 31/496A61K 31/4704A61P 1/08A61P 15/00
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Claims
Abstract
The present invention relates to a method of treating a patient suffering from a disorder of the central nervous system associated with 5-HT 1A receptor subtype, comprising as an active ingredient a carbostyril derivative or a salt thereof represented by the formula (1) wherein the carbon-carbon bond between 3- and 4-positions in the carbostyril skeleton is a single or a double bond.
Claims
exact text as granted — not AI-modified1 . A method of treating a patient suffering from a disorder-of the central nervous system associated with 5-HT 1A receptor subtype, selected from
(i) bipolar I disorder with most recent hypomanic, manic, mixed, depressed or unspecified episode, and (ii) bipolar II disorder with recurrent major depressive episodes with hypomanic episodes, and cyclothymic disorder, which comprises administering to said patient a therapeutically effective amount of a carbostyril compound of formula (1), or a pharmaceutically acceptable salt or solvate thereof, wherein said patient is a mammal:
wherein the carbon-carbon bond between 3- and 4-positions in the carbostyril skeleton is a single or a double bond.
2 . The method of claim 1 , wherein the disorder is bipolar I disorder as defined in (i).
3 . The method of claim 1 , wherein the disorder is bipolar II disorder as defined in (ii).
4 . (canceled)
5 . The method according to claim 1 , wherein the carbostyril compound is
7-{4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy}-3,4-dihydrocarbostyril.
6 . The method according to claim 2 , wherein the
7-{4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy}-3,4-dihydrocarbostyril.
7 . The method according to claim 3 , wherein the carbostyril compound is 7-{4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy}-3,4-dihydrocarbostyril.
8 . (canceled)Cited by (0)
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