发明名称 NEW BICYCLONUCLEOSIDE ANALOG
摘要 <p>PROBLEM TO BE SOLVED: To provide a new bicyclonucleoside analog having anti-AIDS activity and provide an intermediate for the production of an oligonucleotide analog having excellent antisense or antigene activity and stable in living body. SOLUTION: The objective compound is expressed by structural formula (1) [R1 groups are each same or different H or hydroxyl-protecting group; R2 is azide group, a (protected)amino or the like; B is purin-9-yl or 2-oxo-1,2- dihydropyrimidin-1-yl which may have substituent selected from halogen atom, 1-6C alkyl, hydroxyl, mercapto, amino or the like] or its pharmacologically permissible salt.</p>
申请公布号 JP2001089496(A) 申请公布日期 2001.04.03
申请号 JP20000218496 申请日期 2000.07.19
申请人 SANKYO CO LTD 发明人 IMANISHI TAKESHI;OBIKA SATOSHI
分类号 C07H19/06;A61K31/70;A61K31/7042;A61K31/7052;A61K31/7064;A61K31/7072;A61K31/7076;A61K31/712;A61K31/7125;A61P31/18;C07H19/067;C07H19/16;C07H19/167;C07H21/00;(IPC1-7):C07H19/06 主分类号 C07H19/06
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