FIELD: chemistry.
SUBSTANCE: present invention relates to compounds of formula I, in free form of in form of a pharmaceutically acceptable salt. In formula I Ar is phenyl, substituted with a cyano group, R1 is phenyl, optionally substituted with one or more substitutes selected from halogen, cyano, C1-C8-alkoxy, carboxy, or R1 is furanylcarbonyl or phenylcarbonyl, or R1 is a 6-member N-heterocyclic group with one or two nitrogen atoms in the ring, optionally substituted with C1-C4-alkyl or C1-C4-alkoxy, R2 is hydrogen, and Y is a pyrimidinyl or pyridazinyl group, optionally substituted with at least one C1-C8-alkyl or di(C1-C8-alkyl)amino group.
EFFECT: invention relates to a pharmaceutical composition with antagonistic effect on A2b receptor, containing the disclosed compound as an active agent, to use of the disclosed compound in making a medicinal agent with antagonistic effect on A2b receptor and to use of the disclosed compound in making a medicinal agent for treating inflammatory or obstruction respiratory tract diseases.
6 cl, 16 ex
Title | Year | Author | Number |
---|---|---|---|
BICYCLIC HETEROCYCLIC COMPOUNDS AS ANTI-INFLAMMATORY AGENTS | 2006 |
|
RU2426733C2 |
PYRROLIDINIUM DERIVATIVES AS M3 MUSCARINIC RECEPTORS | 2005 |
|
RU2412183C2 |
DERIVATIVES OF NAPHTHYRIDINE, METHOD FOR THEIR PREPARING AND USING | 2002 |
|
RU2296764C2 |
DERIVATIVES OF AZETHIDINE AS ANTAGONISTS OF CCR-3 RECEPTOR | 2003 |
|
RU2314292C2 |
NEW FIVE-MEMBER HETEROCYCLES, THEIR PREPARING, THEIR APPLYING AND PHARMACEUTICAL PREPARATIONS COMPRISING THEREOF | 1998 |
|
RU2240326C2 |
COMBINATIONS OF GLUCOPYRROLATE AND B-2 ADRENOCEPTOR ANTOGONISTS | 2005 |
|
RU2388465C2 |
2-PHENYL-OXAZOLE-4-CARBOXAMIDE DERIVATIVES, MODULATING ACTIVITY OF JAK AND TYK2 KINASE | 2013 |
|
RU2652795C2 |
LIQUID COMPOSITIONS | 2006 |
|
RU2428180C2 |
QUINAZOLINE DERIVATIVES | 2004 |
|
RU2356896C2 |
NOVEL DERIVATIVES OF IMIDAZOLIDINE, THEIR PREPARING AND USING AS VLA-4 ANTAGONIST | 2002 |
|
RU2318815C2 |
Authors
Dates
2009-11-27—Published
2005-01-20—Filed