FIELD: chemistry.
SUBSTANCE: compound, represented by formula
,
or its pharmaceutically acceptable salt, where Y1 represents nitrogen atom or group, represented by CRA, Y2 represents nitrogen atom or group, represented by CRB, Y3 represents nitrogen atom or group, represented by CRC, RA, RB and RC, which can be similar or different, each represents hydrogen atom, etc. (except in the case, when Y1 is CRA, Y2 is CRB and Y3 is CRC), X represents oxygen atom, etc., R1 represents C1-C6alkyl group, etc., R3 represents optionally substituted phenyl group, etc., R4 represents hydrogen atom, etc., and R5 represents optionally substituted phenyl group, etc.), possesses inhibiting action with respect to S1P binding with its receptor Edg-1(SlP1).
EFFECT: obtaining composition, which can be used as therapeutic medication in case of autoimmune diseases, rheumatoid arthritis, asthma, atopic dermatitis, rejection after organ transplantation, cancer, retinopathy, psoriasis, osteoarthritis or age-related macula lutea degeneration, etc.
13 cl, 9 ex, 1 tbl, 4 dwg
Title | Year | Author | Number |
---|---|---|---|
SPHINGOSINE-1-PHOSPHATE BINDING INHIBITOR | 2007 |
|
RU2395499C2 |
TRIAZOLE DERIVATIVES | 2007 |
|
RU2409570C2 |
TRIAZOLE DERIVATIVE | 2005 |
|
RU2383536C2 |
BICYCLIC COMPOUND | 2013 |
|
RU2640416C2 |
DERIVATIVE OF AMINOCARBON ACID AND APPLICATION OF SAID SUBSTANCES FOR MEDICAL PURPOSES | 2005 |
|
RU2433121C2 |
PYRAZOLE COMPOUNDS AS SIGMA RECEPTOR INHIBITORS | 2011 |
|
RU2582338C2 |
1,2,4-TRIAZOLONE DERIVATIVE | 2011 |
|
RU2566754C2 |
3-ALKYLIDENHYDRAZINO-HETEROARYL COMPOUNDS AS ACTIVATORS OF THROMBOPROTEIN RECEPTOR | 2004 |
|
RU2358970C2 |
CYNNAMIDE COMPOUND | 2005 |
|
RU2361872C2 |
SUBSTITUTED ACRYLAMIDE DERIVATIVE AND PHARMACEUTICAL COMPOSITION BASED ON SAID DERIVATIVE | 2006 |
|
RU2404966C2 |
Authors
Dates
2012-11-27—Published
2008-08-01—Filed