发明授权
US5374652A 2-oxindole compounds which are useful as tyrosine kinase inhibitors
失效
可用作酪氨酸激酶抑制剂的2-羟吲哚化合物
- 专利标题: 2-oxindole compounds which are useful as tyrosine kinase inhibitors
- 专利标题(中): 可用作酪氨酸激酶抑制剂的2-羟吲哚化合物
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申请号: US126687申请日: 1993-09-27
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公开(公告)号: US5374652A公开(公告)日: 1994-12-20
- 发明人: Franco Buzzetti , Antonio Longo , Maristella Colombo
- 申请人: Franco Buzzetti , Antonio Longo , Maristella Colombo
- 申请人地址: ITX Milan
- 专利权人: Farmitalia Carlo Erba S r l
- 当前专利权人: Farmitalia Carlo Erba S r l
- 当前专利权人地址: ITX Milan
- 优先权: GBX9004483.5 19900228
- 主分类号: A61K31/16
- IPC分类号: A61K31/16 ; A61K31/03 ; A61K31/19 ; A61K31/22 ; A61K31/275 ; A61K31/40 ; A61K31/403 ; A61K31/404 ; A61K31/415 ; A61K31/4155 ; A61K31/4164 ; A61K31/4178 ; A61K31/425 ; A61K31/44 ; A61K31/4427 ; A61K31/47 ; A61K31/4709 ; A61K31/4725 ; A61P35/00 ; A61P43/00 ; C07C57/42 ; C07C57/60 ; C07C59/52 ; C07C59/54 ; C07C59/64 ; C07C69/017 ; C07C209/42 ; C07C215/48 ; C07C233/11 ; C07C235/34 ; C07C255/34 ; C07C255/36 ; C07C255/37 ; C07C255/41 ; C07C255/52 ; C07C255/53 ; C07C255/54 ; C07C327/44 ; C07C327/48 ; C07D209/34 ; C07D215/12 ; C07D215/14 ; C07D215/20 ; C07D215/22 ; C07D215/227 ; C07D215/233 ; C07D215/26 ; C07D401/06 ; C07D403/06 ; C07D417/06
摘要:
Aryl- and heteroarylethenylene derivatives of formula ##STR1## wherein Y is a mono- or bicyclic ring system chosen from (A), (B), (C), (D), (E), (F) and (G) ##STR2## R is a group of formula R.sub.1 is hydrogen, C.sub.1 -C.sub.6 alkyl or C.sub.2 -C.sub.6 alkanoyl; R.sub.2 is hydrogen, halogen, cyano or C.sub.1 -C.sub.6 alkyl;n is zero or an integer of 1 to 3: n is zero or an integer of 1 to 3 when Y is a ring system (A); it is zero, 1 or 2 when Y is a ring system (B), (E), (F) or (G); or it is zero or 1 when Y is a ring system (C) or (D); and the pharmaceutically acceptable salts thereof; and wherein each of the substituents R, OR.sub.1 and R.sub.2 may be independently on either of the aryl or heteroaryl moieties of the bicyclic ring system (A), (E), (F) and (G), whereas only the benzene moiety may be substituted in the bicyclic ring system (B), are useful as tyrosine kinase activity inhibitors.
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