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Title:
4-(4-PYRIDAZINYL)PYRAZOLE DERIVATIVE
Document Type and Number:
Japanese Patent JP2005022972
Kind Code:
A
Abstract:

To provide a compound having a p38MAP kinase inhibiting action, therefore having the action of inhibiting the production of TNF-α, IL-1, IL-6, COX-II, etc., and being useful as a therapeutic agent against TNF-α-associated diseases, IL-1-associated diseases, IL-6-associated diseases, COX-II-associated diseases, etc.

The above compound is a pyridazinylpyrazole derivative represented by formula (1) (wherein Q is an optionally substituted aryl group or the like; R1 is a hydrogen atom, a lower alkoxyl group, or the like; R2 is a hydrogen atom or an optionally hydroxy-substituted lower alkyl group; and R3 is a hydrogen atom, a lower alkyl group, or the like) or a salt thereof.


Inventors:
MINAMI NOBUYOSHI
HASUMI KOICHI
OTA SHUJI
SATO HIDEICHIRO
SAITOU NORIHISA
DOI SATORU
KOBAYASHI MOTOHIRO
SATO JUN
ASANO SO
MATSUMOTO YASUHIRO
Application Number:
JP2001146270A
Publication Date:
January 27, 2005
Filing Date:
May 16, 2001
Export Citation:
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Assignee:
TEIKOKU HORMONE MFG CO LTD
International Classes:
C07D401/14; A61K31/501; A61P1/00; A61P1/04; A61P1/18; A61P3/10; A61P7/00; A61P7/02; A61P9/04; A61P9/08; A61P9/10; A61P11/00; A61P11/06; A61P13/12; A61P15/06; A61P17/00; A61P17/04; A61P17/06; A61P19/02; A61P19/06; A61P19/08; A61P19/10; A61P25/00; A61P25/28; A61P29/00; A61P29/02; A61P31/18; A61P33/06; A61P35/00; A61P37/02; A61P43/00; C07D403/04; C07D405/14; (IPC1-7): C07D401/14; A61K31/501; A61P1/00; A61P1/04; A61P1/18; A61P3/10; A61P7/00; A61P7/02; A61P9/04; A61P9/08; A61P9/10; A61P11/00; A61P11/06; A61P13/12; A61P15/06; A61P17/00; A61P17/04; A61P17/06; A61P19/02; A61P19/06; A61P19/08; A61P19/10; A61P25/00; A61P25/28; A61P29/00; A61P29/02; A61P31/18; A61P33/06; A61P35/00; A61P37/02; A61P43/00; C07D403/04; C07D405/14
Attorney, Agent or Firm:
Heikichi Odashima
Youji Esumi