发明授权
US5714486A Methods for using (2-imidazolin-2-ylamino) quinoxaline derivatives
失效
使用(2-咪唑啉-2-基氨基)喹喔啉衍生物的方法
- 专利标题: Methods for using (2-imidazolin-2-ylamino) quinoxaline derivatives
- 专利标题(中): 使用(2-咪唑啉-2-基氨基)喹喔啉衍生物的方法
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申请号: US695103申请日: 1996-08-07
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公开(公告)号: US5714486A公开(公告)日: 1998-02-03
- 发明人: James A. Burke , Michael E. Garst , Larry A. Wheeler
- 申请人: James A. Burke , Michael E. Garst , Larry A. Wheeler
- 申请人地址: TX Naco
- 专利权人: Allergan
- 当前专利权人: Allergan
- 当前专利权人地址: TX Naco
- 主分类号: C07D401/12
- IPC分类号: C07D401/12 ; A61K31/495 ; A61K31/498 ; A61P1/12 ; A61P1/14 ; A61P9/00 ; A61P9/10 ; A61P9/12 ; A61P11/02 ; A61P13/02 ; A61P13/12 ; A61P15/00 ; A61P23/00 ; A61P23/02 ; A61P25/00 ; A61P25/02 ; A61P25/04 ; A61P27/16 ; A61P29/00 ; C07D403/12
摘要:
A method of treating a mammal comprises administering to a mammal an effective amount to provide a desired therapeutic effect in the mammal of a compound selected from the group consisting of those having the formula: ##STR1## and pharmaceutically acceptable acid addition salts thereof and mixtures thereof, wherein R.sub.1 and R.sub.2 each is selected from the group consisting of alkyl radicals containing 1 to 4 carbon atoms and alkoxy radicals containing 1 to 4 carbon atoms, the 2-imidazolin-2-ylamino group may be in any of the 5-, 6-, 7- or 8-positions of the quinoxaline nucleus, and R.sub.3, R.sub.4 and R.sub.5 is each located in one of the remaining 5-, 6-, 7- or 8-positions of the quinoxaline nucleus and is independently selected from the group consisting of Cl, Br, H and alkyl radicals containing 1 to 3 carbon atoms. Such compounds, when administered to a mammal, provide anesthetization of the central nervous system.
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