发明申请
US20070129544A1 Novel heteroaryl substituted piperidine derivatives which are L-CPT1 inhibitors
失效
新的杂芳基取代的哌啶衍生物是L-CPT1抑制剂
- 专利标题： Novel heteroaryl substituted piperidine derivatives which are L-CPT1 inhibitors
- 专利标题（中）： 新的杂芳基取代的哌啶衍生物是L-CPT1抑制剂
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申请号： US11605904申请日： 2006-11-29
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公开(公告)号： US20070129544A1公开(公告)日： 2007-06-07
- 发明人: Jean Ackermann , Konrad Bleicher , Simona Ceccarelli Grenz , Odile Chomienne , Patrizio Mattei , Tanja Schulz-Gasch
- 申请人： Jean Ackermann , Konrad Bleicher , Simona Ceccarelli Grenz , Odile Chomienne , Patrizio Mattei , Tanja Schulz-Gasch
- 优先权： EP05111560.8 20051201
- 主分类号： A61K31/541
- IPC分类号： A61K31/541 ; A61K31/5377 ; A61K31/496 ; C07D417/14 ; C07D413/14
摘要：
The invention is concerned with novel substituted piperidine derivatives of formula (I) wherein R1, R2, R3, R4, R5, R6, R7 and X are as defined in the description and in the claims, as well as physiologically acceptable salts and esters thereof. These compounds inhibit L-CPT1 and can be used as medicaments.