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Title:
SUBSTITUTED TRIAZOLO-PYRIDAZINE DERIVATIVE
Document Type and Number:
Japanese Patent JP2013100322
Kind Code:
A
Abstract:

To provide a method of treating a disease and a condition that are beneficially treated by administering an α1-GABA-A receptor antagonist and/or α2, α3 and α5 GABA-A receptor agonists.

There are provided substituted triazolo-pyridazines represented by formula 1, derivatives of the same, and pharmaceutically acceptable salts thereof. (In formula, R1 is CH3, CDH2, CD2H, or CD3; R2 is a t-butyl group having 0-9 deuterium atoms; each Y is independent and is hydrogen or deuterium; and R2 has 1-9 deuterium atoms when R1 is CH3 and each Y is hydrogen).


Inventors:
HARBESON SCOTT
Application Number:
JP2013004449A
Publication Date:
May 23, 2013
Filing Date:
January 15, 2013
Export Citation:
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Assignee:
CONCERT PHARMACEUTICALS INC
International Classes:
C07D487/04; A61K31/5025; A61K45/00; A61P21/02; A61P25/04; A61P25/06; A61P25/22; A61P25/28; A61P29/00; A61P43/00
Domestic Patent References:
JP2002514169A2002-05-14
JP2002535407A2002-10-22
JP2002514169A2002-05-14
JP2002535407A2002-10-22
Foreign References:
WO2006061428A22006-06-15
WO2006061428A22006-06-15
Other References:
JPN6013014075; MCKERNAN,R.M. et al.: 'Sedative but not anxiolytic properties of benzodiazepines are mediated by the GABA(A) receptor alpha' Nat.Neurosci. Vol.3, No.6, 2000, p.587-592
JPN6013014075; MCKERNAN,R.M. et al.: 'Sedative but not anxiolytic properties of benzodiazepines are mediated by the GABA(A) receptor alpha' Nat.Neurosci. Vol.3, No.6, 2000, p.587-592
Attorney, Agent or Firm:
Ryoichi Takaoka
Nao Oda