发明授权
- 专利标题: Substituted pyrazolo[3,4-d]pyrimidinone derivatives
- 专利标题(中): 取代的吡唑并[3,4-d]嘧啶酮衍生物
-
申请号: US11789548申请日: 2007-04-25
-
公开(公告)号: US07834019B2公开(公告)日: 2010-11-16
- 发明人: Takeshi Sagara , Sachie Otsuki , Satoshi Sunami , Toshihiro Sakamoto , Kenji Niiyama , Fuyuki Yamamoto , Takashi Yoshizumi , Hidetomo Furuyama , Yasuhiro Goto , Makoto Bamba , Keiji Takahashi , Hiroshi Hirai , Toshihide Nishibata
- 申请人: Takeshi Sagara , Sachie Otsuki , Satoshi Sunami , Toshihiro Sakamoto , Kenji Niiyama , Fuyuki Yamamoto , Takashi Yoshizumi , Hidetomo Furuyama , Yasuhiro Goto , Makoto Bamba , Keiji Takahashi , Hiroshi Hirai , Toshihide Nishibata
- 申请人地址: JP Chiyoda-Ku, Tokyo
- 专利权人: Banyu Pharmaceutical Co., Ltd.
- 当前专利权人: Banyu Pharmaceutical Co., Ltd.
- 当前专利权人地址: JP Chiyoda-Ku, Tokyo
- 代理商 Nicole M. Beeler
- 主分类号: A61K31/519
- IPC分类号: A61K31/519 ; A61K31/497 ; C07D487/04 ; A61P35/00
摘要:
The invention relates to compounds of a general formula (I): wherein Ar1 is an optionally-substituted aryl or heteroaromatic group; R1 is an optionally-substituted lower alkyl, lower alkenyl, lower alkynyl or cyclo-lower alkyl group, or is an aryl, aralkyl or heteroaromatic group optionally having a substituent; R2 is a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group, or is an aryl, aralkyl or heteroaromatic group optionally having a substituent; R3 is a hydrogen atom or a lower alkyl group; R4 is a hydrogen atom, a halogen atom, a hydroxyl group, a lower alkyl group or a group of —N(R1k)R1m; T and U are a nitrogen atom or a methine group, etc. The compounds of the invention have excellent Weel kinase-inhibitory effect and are therefore useful in the field of medicines, especially treatment of various cancers.
公开/授权文献
- US20070254892A1 Dihydropyrazolopyrimidinone derivatives 公开/授权日:2007-11-01
信息查询
IPC分类: