发明申请
US20060148798A1 N-phenylpyrrole guanidine derivatives as melanocortin receptor ligands
失效
N-苯基吡咯胍衍生物作为黑皮质素受体配体
- 专利标题: N-phenylpyrrole guanidine derivatives as melanocortin receptor ligands
- 专利标题(中): N-苯基吡咯胍衍生物作为黑皮质素受体配体
-
申请号: US11374956申请日: 2006-03-15
-
公开(公告)号: US20060148798A1公开(公告)日: 2006-07-06
- 发明人: Torbjorn Lundstedt , Anna Skottner , Arne Boman , Per Andersson , Elisabeth Seifert , Victor Andrianov
- 申请人: Torbjorn Lundstedt , Anna Skottner , Arne Boman , Per Andersson , Elisabeth Seifert , Victor Andrianov
- 申请人地址: DK Arhus N
- 专利权人: ACTION PHARMA A/S
- 当前专利权人: ACTION PHARMA A/S
- 当前专利权人地址: DK Arhus N
- 优先权: GB0119172.5 20010806
- 主分类号: A61K31/5377
- IPC分类号: A61K31/5377 ; A61K31/4025 ; C07D413/02 ; C07D403/02 ; C07D207/30
摘要:
The present invention provides novel compounds of the general Formula (I) as ligands to the melanocortin receptors and/or for treatment of disorders in the melanocortin system: wherein X is (CH2)n where n is 0, 1 or 2; R1, R2, R3, R4 and R5 may be the same or different and are selected from hydrogen, halogen, alkyl having 1 to 5 carbon atoms, alkoxy having 1 to 5 carbon atoms, hydroxy, alkylsulphonyloxy, cyano, nitro, trihaloalkyl, sulpho or one of the structures given in Scheme 1; or two of R1, R2, R3, R4 and R5 may together form a methylenedioxy or ethylenedioxy moiety; R6, R7, R8 and R9 are the same or different and are selected from hydrogen, halogen, alkyl having 1 to 5 carbon atoms, alkoxy having 1 to 5 carbon atoms, hydroxy, amines (primary, secondary or tertiary) having 0, 1 or 2 carbon atoms, cyano, nitro, trihaloalkyl, amide or sulpho, and z where shown represents the point of attachment of the residue to the phenyl or pyrrole ring; and the pharmacologically active salts thereof.
公开/授权文献
信息查询
IPC分类: