发明授权
US07745453B2 Hydroxypyrimidinone derivatives having inhibitory activity against HIV integrase
有权
具有对HIV整合酶的抑制活性的羟基嘧啶酮衍生物
- 专利标题: Hydroxypyrimidinone derivatives having inhibitory activity against HIV integrase
- 专利标题(中): 具有对HIV整合酶的抑制活性的羟基嘧啶酮衍生物
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申请号: US10583796申请日: 2004-12-21
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公开(公告)号: US07745453B2公开(公告)日: 2010-06-29
- 发明人: Hidenori Mikamiyama , Minamo Iwata , Yoshiyuki Taoda
- 申请人: Hidenori Mikamiyama , Minamo Iwata , Yoshiyuki Taoda
- 申请人地址: JP Osaka
- 专利权人: Shionogi & Co., Ltd.
- 当前专利权人: Shionogi & Co., Ltd.
- 当前专利权人地址: JP Osaka
- 代理机构: Wenderoth, Lind & Ponack, L.L.P.
- 优先权: JP2003-423947 20031222
- 国际申请: PCT/JP2004/019048 WO 20041221
- 国际公布: WO2005/061490 WO 20050707
- 主分类号: A61K31/505
- IPC分类号: A61K31/505 ; C07D239/02 ; C07D401/00 ; C07D403/00 ; C07D405/00 ; C07D409/00 ; C07D411/00 ; C07D413/00 ; C07D417/00 ; C07D419/00
摘要:
Compounds of Formula (1), pharmaceuticals containing the same, especially anti-HIV agents having anti viral activity, especially inhibitory activity against HIV integrase, wherein X represents either one of the following groups: (wherein, C ring is nitrogen-containing aromatic heterocyclic ring in which at least one atom in atoms neighboring the atom bound to the pyrimidine ring is unsubstituted nitrogen atom; R10 is hydrogen or lower alkyl; D ring is aryl or heteroaryl) Z1 and Z3 each is independently a single bond, O, S, S(═O) or SO2; Z2 is a single bond, lower alkylene or lower alkenylene; Ar is optionally substituted aryl or optionally substituted heteroaryl; R1 is lower alkyl, substituted lower alkyl or the like; R2 is a hydrogen atom or optionally substituted lower alkyl; or R1 and R2 may form, together with an adjacent atom, an optionally substituted heterocyclic ring, a pharmaceutically acceptable salt or a solvate thereof.
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