发明公开
- 专利标题: N-2 SUBSTITUTED PURINES
- 专利标题(中): N-2取代的嘌呤
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申请号: EP95902698.0申请日: 1994-11-29
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公开(公告)号: EP0731807A1公开(公告)日: 1996-09-18
- 发明人: COOK, Phillip, Dan , RAMASAMY, Kanda, S. , MANOHARAN, Muthiah
- 申请人: ISIS PHARMACEUTICALS, INC.
- 申请人地址: 2280 Faraday Avenue Carlsbad, CA 92008 US
- 专利权人: ISIS PHARMACEUTICALS, INC.
- 当前专利权人: ISIS PHARMACEUTICALS, INC.
- 当前专利权人地址: 2280 Faraday Avenue Carlsbad, CA 92008 US
- 代理机构: Hallybone, Huw George
- 优先权: US19930159088 19931129
- 国际公布: WO1995014707 19950601
- 主分类号: C07D473
- IPC分类号: C07D473 ; A61K31 ; A61K47 ; A61P31 ; C07D487 ; C07H19 ; C07H21 ; C07H23 ; C07J43 ; C12N9 ; C12N15 ; C12Q1 ; A61K38 ; A61K48
摘要:
This invention presents novel purine-based compounds for inclusion into oligonucleotides. The compounds of the invention, when incorporated into oligonucleotides are especially useful as 'antisense' agents -- agents that are capable of specific hybridization with a nucleotide sequence of an RNA. Oligonucleotides are used for a variety of therapeutic and diagnostic purposes, such as treating diseases, regulating gene expression in experimental systems, assaying for RNA and for RNA products through the employment of antisense interactions with such RNA, diagnosing diseases, modulating the production of proteins, and cleaving RNA in site specific fashions. The compounds of the invention include novel heterocyclic bases, nucleosides, and nucleotides. When incorporated into oligonucleotides, the compounds of the invention can be useful for modulating the activity of RNA.
公开/授权文献
- EP0731807B1 N-2 SUBSTITUTED PURINES 公开/授权日:2004-03-17
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