FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to compounds of formula or their pharmaceutically acceptable salts, wherein Xa represents N or CH; R1e represents C1-6-alkyl optionally substituted by aryl specified in phenyl, naphthyl, fenanthryl and anthryl, or by halogen; C1-6-alkoxy optionally substituted by aryl specified in phenyl, naphthyl, fenanthryl and anthryl, by halogen or C3-8-cycloalkyl; C2-6-alkenyl; C3-8-cycloalkyl; or halogen; R1f represents hydrogen, C1-6-alkyl, C1-6-alkoxy, hydroxyl, cyano or halogen; R21 represents 5-10-merous heteroaryl, which has 1-3 heteroatoms specified in nitrogen, oxygen or sulphur, and which can be substituted by identical or different 1-3 groups specified in the patent claim; R31 represents 6-merous heteroaryl, which has 1 or 2 nitrogen atoms, and which can be substituted by identical or different 1-3 groups specified in the patent claim. The invention also refers to an antithrombotic agent and a medicinal product containing the compounds of formula IIa as an active ingredient, to a method for preventing thrombocyte aggregation, and a method for preventing or treating ischemic stroke, acute coronary syndrome, microvascular dysfunction, peripheral arterial disease, arteriosclerosis obliterans, ischemic heart disease, thrombotic microangiopathy, or unstable or stable angina.
EFFECT: compounds of formula IIa exhibiting the inhibitory activity on thrombocyte aggregation.
18 cl, 34 tbl, 192 ex
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Authors
Dates
2015-12-10—Published
2010-12-17—Filed