首页> 外国专利> THIAZINE OR THIAZEPINE DERIVATIVES USEFUL AS INHIBITORS OF NO-SYNTHETASE

THIAZINE OR THIAZEPINE DERIVATIVES USEFUL AS INHIBITORS OF NO-SYNTHETASE

机译:噻嗪或噻嗪酮衍生物可作为NO合成抑制剂

摘要

The subject of the invention is thiazine or thiazepine derivatives of the following general formula (I) and their pharmaceutically acceptable salts BR/ (CF DRAWING IN BOPI) BR/ in which R ** 1 is a hydrogen atom, a substituted or unsubstituted alkyl group, a cycloalkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted heteroaryl group, or an aralkyl group substituted or unsubstituted; R ** 2, R ** 3, R ** 4 and R ** 5, which may be the same or different, are each a hydrogen atom, a substituted or unsubstituted alkyl group; or R ** 1 taken together with R ** 2 or R ** 3 may represent BR/ - (CH2) n - BR/ where n is an integer of 1 to 6; BR/ A is an oxygen atom, a sulfur atom or an NH group; m is 0 or 1; and BR/ p is 0 or 1. BR/ These compounds have NO-synthetase inhibitory activity and can be used in the treatment of conditions related to excessive production of nitric oxide in vivo . / P
机译:本发明的主题是以下通式(I)的噻嗪或噻嗪类衍生物及其药学上可接受的盐
(CF DRAWING IN BOPI)
其中R ** 1是氢原子,或未取代的烷基,环烷基,取代或未取代的烯基,取代或未取代的炔基,取代或未取代的芳基,取代或未取代的杂芳基或取代或未取代的芳烷基;或可以相同或不同的R ** 2,R ** 3,R ** 4和R ** 5各自为氢原子,取代或未取代的烷基。或R ** 1与R ** 2或R ** 3一起代表
-(CH2)n-
其中n为1至6的整数;或
A是氧原子,硫原子或NH基。 m为0或1;并且
p为0或1。
这些化合物具有NO合成酶抑制活性,可用于治疗与体内一氧化氮过量产生有关的疾病。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号