您的位置: 首页 > 农业专利 > 详情页

具HIV接合酶抑制活性之聚環性胺甲醯基吡啶酮衍生物
专利权人:
SHIONOGI & CO., LTD.;SMITHKLINE BEECHAM CORPORATION
发明人:
JOHNS, BRIAN, ALVIN,琼斯布莱恩艾文,瓊斯布萊恩艾文,KAWASUJI, TAKASHI,川筋孝,TAISHI, TERUHIKO,大司照彦,大司照彥,TAODA, YOSHIYUKI,垰田善之
申请号:
TW095115285
公开号:
TWI378931B
申请日:
2006.04.28
申请国别(地区):
TW
年份:
2012
代理人:
摘要:
The present invention is to provide a novel compound (I) shown below, having the anti-virus activity, particularly the HIV integrase inhibitory activity, and a drug containing the same, particularly an anti-HIV drug, as well as a process and an intermediate thereof. (wherein Z 1 is NR 4 ; R 1 is hydrogen or lower alkyl; X is a single bond, a hetero atom group selected from O, S, SO, SO 2 and NH, or lower alkylene or lower alkenylene in which the hetero atom group may intervene; R 2 is optionally substituted aryl; R 3 is hydrogen, a halogen, hydroxy, optionally substituted lower alkyl etc; and R 4 and Z 2 part taken together forms a ring, to form a polycyclic compound, including e.g., a tricyclic or tetracyclic compound.本發明提供一種如下示之新穎化合物(I),其具有抗病毒活性,特別是HIV接合酶抑制活性,及含其之藥劑,特別是抗-HIV藥劑,與其之製造方法及中間產物。;(I);(其中;Z1為NR4;R1為氫或低級烷基;X為單鍵、選自O、S、SO、SO2及NH之雜原子、或可插入雜原子基之低級伸烷基或低級伸烯基;R2為選擇性經取代之芳基;R3為氫、鹵素、羥基、選擇性經取代之低級烷基等;且R4與Z2部分一起形成一環、形成一聚環性化合物,包括例如三環狀或四環狀化合物。
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

意 见 箱

匿名:登录

个人用户登录

找回密码

第三方账号登录

忘记密码

个人用户注册

必须为有效邮箱
6~16位数字与字母组合
6~16位数字与字母组合
请输入正确的手机号码

信息补充