发明名称 |
SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-PYRIDO[4,3-B]INDOLES, METHODS FOR USE THEREOF |
摘要 |
The present invention relates to a method of antagonizing a 5-HT6 serotonin receptor, comprising administering to the cell a compound of formula 1.2, or a pharmaceutically acceptable salt thereof,;;wherein: R1 is a C1-C5 alkyl;
R2i is independently hydrogen, halogen, a C1-C3 alkyl, CF3, OCF3 or OCH3;i is 1, 2, 3 or 4;Ar is an unsubstituted phenyl or a substituted phenyl substituted with halogen, C1-C6 alkyl, C1-C6 alkoxy, substituted amino group or trifluoromethyl; or Ar is a substituted or unsubstituted 6-membered aromatic heterocycle with one or two nitrogen atoms in the heterocycle.;The invention also relates to pharmaceutical compositions and method for treating a cognitive disorder or neurodegenerative disease in a subject in need thereof comprising administering an effective dose to the subject of a compound of formula 1.2 according to claim 1, or a pharmaceutically acceptable salt thereof. |
申请公布号 |
US2017000773(A1) |
申请公布日期 |
2017.01.05 |
申请号 |
US201514791280 |
申请日期 |
2015.07.03 |
申请人 |
Ivachtchenko Alexandre Vasilievich;lvashchenko Andrey Alexandrovich;Savchuk Nikolay Filippovich |
发明人 |
Ivachtchenko Alexandre Vasilievich;lvashchenko Andrey Alexandrovich;Savchuk Nikolay Filippovich |
分类号 |
A61K31/437;A61K31/444 |
主分类号 |
A61K31/437 |
代理机构 |
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代理人 |
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主权项 |
1. A method of antagonizing a 5-HT6 serotonin receptor, comprising administering to the cell a compound of formula 1.2, or a pharmaceutically acceptable salt thereof,wherein: R1 is a C1-C5 alkyl;
R2i is independently hydrogen, halogen, a C1-C3 alkyl, CF3, OCF3 or OCH3; i is 1, 2, 3 or 4; Ar is an unsubstituted phenyl or a substituted phenyl substituted with halogen, C1-C6 alkyl, C1-C6 alkoxy, substituted amino group or trifluoromethyl; or Ar is a substituted or unsubstituted 6-membered aromatic heterocycle with one or two nitrogen atoms in the heterocycle. |
地址 |
Encinitas CA US |