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filingDate 2003-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3b8016ab1f2fa4bddd6798741347ea8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c89bb0f909eb4e4bc781bc99d15b17a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdbef6eeea111ec18fc1e88945409854
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4693ae03f73e22f16109d4eb2a334557
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1edae459d5370f09a945c97816445b5e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8872a55d424f135631d0f759a6bad36c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b1de7297060bc2437cfc37f5ca8946b
publicationDate 2008-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-009710-B1
titleOfInvention ADAMANTYLACETAMIDES AS INHIBITORS 11-BETA HYDROXYSTEROID DEHYDROGENASE
abstract The invention relates to adamantylacetamide formula (I), their N-oxide forms, pharmaceutically acceptable additive salts and stereochemically isomeric forms, where n is an integer equal to 1; m is an integer equal to 0 or 1; R1 and R2, each independently, represents C1-6 alkyl; or R and R together with the carbon atom to which they are attached, form Cycloalkyl; R3 is an optionally substituted adamantyl of formula (a) or (b); Q is an optionally substituted phenyl, benzothiophenyl, or pyridyl; L is Salkyl. In addition, the invention relates to a pharmaceutical composition comprising a pharmaceutically acceptable carrier and, as an active ingredient, an effective inhibitory 11β-HSD1 amount of a compound of the invention, a method for preparing it and the use of a compound of the invention for preparing a medicament for treating visceral obesity, insulin sensitivity , type 2 diabetes, hyperlipidemia and hyperphagia.
priorityDate 2002-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 437.