发明名称 |
DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS |
摘要 |
<p>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: trif luoromethyl, halogen such as F, C1, -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 enyzme inhibitors for the treatment of obesitz, tzpe-2 diabetes and lipid disorders.</p> |
申请公布号 |
WO2011015629(A1) |
申请公布日期 |
2011.02.10 |
申请号 |
WO2010EP61426 |
申请日期 |
2010.08.05 |
申请人 |
PIERRE FABRE MEDICAMENT;DUPONT-PASSELAIGUE, ELISABETH;MIALHE, SAMUEL;RIEU, JEAN-PIERRE;JUNQUERO, DIDIER;VALEILLE, KARINE |
发明人 |
DUPONT-PASSELAIGUE, ELISABETH;MIALHE, SAMUEL;RIEU, JEAN-PIERRE;JUNQUERO, DIDIER;VALEILLE, KARINE |
分类号 |
C07D237/22;A61K31/497;A61K31/501;A61P3/00;A61P9/00;A61P17/00;C07D401/12;C07D403/12 |
主分类号 |
C07D237/22 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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