SULFONYLBENZYL-SUBSTITUTED IMIDAZOPYRIDINES
Imidazopyridines of the formula (I) in which R represents alkyl or alkenyl, each of which is optionally substituted by cycloalkyl, or represents cycloalkyl, B and D together form a radical of the formula A represents a 3- to 8-membered, saturated heterocycle bonded via the nitrogen atom and having u...
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creator | KNORR ANDREAS DR FEY PETER DR HUBSCH WALTER DR WOHLFEIL STEFAN DR STASCH JOHANNES-PETER DR HANKO RUDOLF DR MULLER ULRICH E. DR MULLER-GLIEMANN MATTHIAS DR KAZDA STANISLAV DR HIRTH-DIETRICH CLAUDIA DR YALKINOGLU OZKAN DR DRESSEL JURGEN PH.D KRAMER THOMAS DR BEUCK MARTIN DR |
description | Imidazopyridines of the formula (I) in which R represents alkyl or alkenyl, each of which is optionally substituted by cycloalkyl, or represents cycloalkyl, B and D together form a radical of the formula A represents a 3- to 8-membered, saturated heterocycle bonded via the nitrogen atom and having up to two further heteroatoms from the group consisting of S, N and O and which is optionally substituted up to 2 times by identical or different perfluoroalkyl having up to 5 carbon atoms or by a radical of the formula The sulphonylbenzyl-substituted imidazopyridines can be employed as active compounds in medicaments, in particular for the treatment of hypertension and atherosclerosis. |
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DR</creatorcontrib><creatorcontrib>MULLER-GLIEMANN MATTHIAS DR</creatorcontrib><creatorcontrib>KAZDA STANISLAV DR</creatorcontrib><creatorcontrib>HIRTH-DIETRICH CLAUDIA DR</creatorcontrib><creatorcontrib>YALKINOGLU OZKAN DR</creatorcontrib><creatorcontrib>DRESSEL JURGEN PH.D</creatorcontrib><creatorcontrib>KRAMER THOMAS DR</creatorcontrib><creatorcontrib>BEUCK MARTIN DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KNORR ANDREAS DR</au><au>FEY PETER DR</au><au>HUBSCH WALTER DR</au><au>WOHLFEIL STEFAN DR</au><au>STASCH JOHANNES-PETER DR</au><au>HANKO RUDOLF DR</au><au>MULLER ULRICH E. DR</au><au>MULLER-GLIEMANN MATTHIAS DR</au><au>KAZDA STANISLAV DR</au><au>HIRTH-DIETRICH CLAUDIA DR</au><au>YALKINOGLU OZKAN DR</au><au>DRESSEL JURGEN PH.D</au><au>KRAMER THOMAS DR</au><au>BEUCK MARTIN DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SULFONYLBENZYL-SUBSTITUTED IMIDAZOPYRIDINES</title><date>1993-12-15</date><risdate>1993</risdate><abstract>Imidazopyridines of the formula (I) in which R represents alkyl or alkenyl, each of which is optionally substituted by cycloalkyl, or represents cycloalkyl, B and D together form a radical of the formula A represents a 3- to 8-membered, saturated heterocycle bonded via the nitrogen atom and having up to two further heteroatoms from the group consisting of S, N and O and which is optionally substituted up to 2 times by identical or different perfluoroalkyl having up to 5 carbon atoms or by a radical of the formula The sulphonylbenzyl-substituted imidazopyridines can be employed as active compounds in medicaments, in particular for the treatment of hypertension and atherosclerosis.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS |
title | SULFONYLBENZYL-SUBSTITUTED IMIDAZOPYRIDINES |
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