Invention Grant
US07709492B2 Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists
有权
吡唑并[4,3-e] -1,2,4-三唑并 - [1,5-c] - 嘧啶腺苷A2a受体拮抗剂
- Patent Title: Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists
- Patent Title (中): 吡唑并[4,3-e] -1,2,4-三唑并 - [1,5-c] - 嘧啶腺苷A2a受体拮抗剂
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Application No.: US11108916Application Date: 2005-04-19
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Publication No.: US07709492B2Publication Date: 2010-05-04
- Inventor: Bernard R. Neustadt , Jinsong Hao , Hong Liu , Craig D. Boyle , Samuel Chackalamannil , Unmesh G. Shah , Andrew Stamford , Joel M. Harris
- Applicant: Bernard R. Neustadt , Jinsong Hao , Hong Liu , Craig D. Boyle , Samuel Chackalamannil , Unmesh G. Shah , Andrew Stamford , Joel M. Harris
- Applicant Address: US NJ Kenilworth
- Assignee: Schering Corporation
- Current Assignee: Schering Corporation
- Current Assignee Address: US NJ Kenilworth
- Agent Krishna G. Banerjee; William Y. Lee; Anita W. Magatti
- Main IPC: A01N43/54
- IPC: A01N43/54 ; A61K31/505 ; C07D239/00 ; C07D487/08
![Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists](/abs-image/US/2010/05/04/US07709492B2/abs.jpg.150x150.jpg)
Abstract:
Compounds having the structural formula I or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl, furanyl, thienyl, pyridyl, pyridyl N-oxide, oxazolyl or pyrrolyl, or cycloalkenyl R1, R2, R3, R4 and R5 are H, alkyl or alkoxyalkyl; and Z is optionally substituted aryl or heteroaryl are disclosed. Also disclosed is the use of compounds of formula I in the treatment of central nervous system diseases, in particular Parkinson's disease, alone or in combination with other agents for treating Parkinson's disease, and pharmaceutical compositions comprising them.
Public/Granted literature
- US20050239795A1 Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2a receptor antagonists Public/Granted day:2005-10-27
Information query
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