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filingDate 1995-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b708d2df53060b42cb00456b1c6ea7c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7bbf84f1b552f28a4e99c4412e7e413
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a85e4be817ca5a382e41852bbaf53b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c18be77a599ee8f468fba1d27ce79cd3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_452611fbc8df110007110fbcf780a85f
publicationDate 2000-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-286739-B6
titleOfInvention Imidazopyridine derivative, process of its preparation and pharmaceutical preparation containing thereof
abstract In the present invention there is disclosed imidazopyridine derivative of the general formula I, in which R represents the group of the general formula a, Re1 represents a fluorine atom, Re2 represents {-SOi2NH-CORe5}, Re3 represents A, Re4 represents {-CinHi2nCO-Nre6Re7}, {-CinHi2nCOOA}, {-CinHi2nCOOH}, {-CinHi2nAr}, {-CinHi2nCOAr} or {-CinHi2nCOA}, Re5 represents A, {-CitHi2t-cycloalkyl} containing 3 to 8 carbon atoms in the cycloalkyl moiety, {-CitHi2t-Ar} or {-O-CitHi2t-Ar}, Re6 and Re7 each represents hydrogen, A, {ArCinHi2n} or Re6 and Re7 together represent also alkylene containing 2 to 5 carbon atoms, A represents alkyl containing 1 to 6 carbon atoms, Ar represents phenyl, t is always zero, 1, 2, 3 or 4, n is 1, 2, 3, 4, 5 or 6. The above-described derivative and physiologically acceptable salts exhibit antagonistic properties against angiotensin II and they are therefore suitable for preparing pharmaceutical preparations intended for treating high pressure of blood, aldosteronism, heart insufficiency and increased intra-ocular pressure and for treating disorders of central nervous system.
priorityDate 1994-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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