发明名称 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS
摘要 The present invention concerns compounds of general formula (I) characterized in that (formula 1) wherein, in particular: —R1 represents one or more groups such as: trifluoromethyl, halogen such as F, Cl, —when n=m=1, W represents CH then Y represents oxygen, —U represents: either —(C═O)CH2NH— and is branched at position 4 of pyridazinone, then R2 represents H, or —(C═O)NH— and U is branched at positions (4), (5) or (6) of pyridazinone, then R2 represents H, —R3 represents a hydrogen or methyl and the addition salts with pharmaceutically acceptable bases and acids and the different isomers, and their mixtures in any proportion for use as SCD-1 enzyme inhibitors for the treatment of obesity, type-2 diabetes and lipid disorders.
申请公布号 US2012178678(A1) 申请公布日期 2012.07.12
申请号 US201013388884 申请日期 2010.08.05
申请人 DUPONT-PASSELAIGUE ELISABETH;MIALHE SAMUEL;RIEU JEAN-PIERRE;JUNQUERO DIDIER;VALEILLE KARINE;PIERRE FABRE MEDICAMENT 发明人 DUPONT-PASSELAIGUE ELISABETH;MIALHE SAMUEL;RIEU JEAN-PIERRE;JUNQUERO DIDIER;VALEILLE KARINE
分类号 A61K31/501;A61K31/513;A61K38/22;A61K38/26;A61K38/28;A61P1/16;A61P3/00;A61P3/04;A61P3/06;A61P3/10;A61P5/28;A61P9/00;A61P9/10;A61P17/00;A61P17/06;A61P17/08;A61P17/10;A61P31/04;A61P35/00;A61P35/02;C07D401/06;C07D401/12;C07D403/12;C12N9/99 主分类号 A61K31/501
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