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filingDate 1992-01-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3f1edad3daaea636e0b8d321e1f77fa
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publicationDate 1992-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0503162-A1
titleOfInvention Azole derivatives, process for their preparation and their application
abstract R¹ (C₂-C₁₀)-Alkyl Z Stickstoff X,Y unabhängig voneinander CR² L -CH₂- q Null oder 1 A Biphenylrest, der z.B. mit R¹⁵ substituiert ist R² Halogen oder Wasserstoff R¹⁵ SO₂-NH-CO-OR⁶ und R⁶ Phenyl, sind hochwirksame Antagonisten von Angiotensin-II-Rezeptoren.Azole derivative of general formula (I), where A, L, O, R 1, X, Y, Z and q have the meanings indicated, processes for their preparation, pharmaceutical preparations and the use of the compounds are described. Azole derivatives of the formula I where the symbols have, for example, the following meanings: R (C₂-C₁₀) -alkyl Z nitrogen X, Y independent of each other CR² L -CH₂- q Zero or 1 A Biphenyl, which is substituted for example with R¹⁵ R Halogen or hydrogen R¹⁵ SO₂-NH-CO-OR⁶ and R⁶ phenyl, are highly potent antagonists of angiotensin II receptors.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393669
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226723783
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID55176
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394073
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393434
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127732581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226679280
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53831061
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87947761
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226432336

Total number of triples: 295.