FIELD: chemistry.
SUBSTANCE: invention refers to 1,2,4,5-tetrasubstituted imidazole derivatives of general formula (I) , where R1 represents chlorine, bromine, fluorine or hydrogen atom, R2 represents chlorine or bromine atom, A represents nitrogen atom or group CH, X represents sulphur atom or sulphoxide (S=O) group, or sulphonic (SO2) group, Y represents hydrogen atom or methyl, ethyl, n-propyl, isopropyl, n-butyl, tert-butyl group, Z represents CH group, n represents number 1,2 or 3, and pharmacologically acceptable salts of compounds. Besides, the invention concerns a pharmaceutical composition based on the compound of general formula (I), to the compounds of general formulas and and to application of compounds of general formula (I).
EFFECT: new imidazole derivatives being selective modulators of cannabinoid receptors CB1 with high selectivity.
12 cl, 1 tbl, 4 ex
Title | Year | Author | Number |
---|---|---|---|
DERIVATIVES OF 1H-IMIDAZOLE POSSESSING CB-AGONISTIC, PARTIAL CB-AGONISTIC OR CB-ANTAGONISTIC ACTIVITY | 2002 |
|
RU2299200C2 |
IMIDAZOLINE DERIVATIVES HAVING CB-ANTAGONIST ACTIVITY | 2005 |
|
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1-IMIDAZOLE DERIVATIVES AS MODULATORS OF CANNABINOID RECEPTORS | 2004 |
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DERIVATIVES OF THIAZOLE POSSESSING ANTAGONISTIC, AGONISTIC OR PARTIALLY AGONISTIC CB-ACTIVITY | 2003 |
|
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DERIVATIVES OF 1H-1,2,4-TRIAZOLE-3-CARBOXAMIDEAS LIGANDS OF RECEPTOR CANNABINOIDS | 2003 |
|
RU2325382C2 |
2-AMINOBENZOTHIAZOLS AS INVERS AGONIST OF CB RECEPTORS | 2004 |
|
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IMIDAZOLE DERIVATIVES ACTIVE TO CB1 RECEPTOR | 2005 |
|
RU2377238C2 |
DERIVATIVES OF 4,5-DIHYDRO-1H-PYRAZOLE POSSESSING CB-ANTAGONISTIC ACTIVITY | 2002 |
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RU2281941C2 |
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RU2420518C2 |
Authors
Dates
2009-05-10—Published
2005-05-26—Filed