FIELD: medicine, pharmaceutics.
SUBSTANCE: present invention refers to new (2R)-2-phenylpropanamide derivatives of formula (I) or their pharmaceutically acceptable salts having an ability to inhibit CXCL1-induced chemiotaxis of human multiform nuclear leucocytes (PMNs), to a based pharmaceutical composition, to applying them for preparing a drug and a methods for making them. wherein R is specified from H, C1-C5-alkyl, C3-C6-cycloalkyl, thiazol substituted by trifluoromethyl, a residue of formula -CH2-CH2-O-(CH2-CH2O)nR", wherein R" represents H or C1-C5-alkyl, n is equal to an integer within 0 to 2, or R together with an NH-group whereto attached is a radical group of primary amides of natural amino acid such as (2S)-2-aminopropanamide; R' is specified in linear or branched C1-C5-alkyl, C3-C6-cycloalkyl, trifluoromethyl, phenyl, optionally substituted by a group specified in halogen, C1-C5-alkyl, C1-C5-alkoxy and trifluoromethyl; unsubstituted benzyl; thiophen.
EFFECT: preparing the new pharmaceutical composition.
9 cl, 1 tbl
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Authors
Dates
2012-07-27—Published
2007-05-17—Filed