发明名称 NOVEL BICYCLONUCLEOSIDE DERIVATIVES
摘要 <p>Compounds of the structural formula (1) or pharmacologically acceptable salts thereof, useful as intermediates for the preparation of nonnatural oligonucleotide analogues or 2-5A analogues which exhibit an excellent antisense or antigene activity and are stable <i>in vivo</i>: wherein R<1> and R<3> are each independently hydrogen, a hydroxyl-protecting group for nucleic acid synthesis, or the like; R<2> is hydrogen, C1-C6 alkyl, or an amino-protecting group for nucleic acid synthesis; and B is a purin-9-yl or 2-oxo-1,2-dihydropyrimidin-1-yl group which may have a substituent selected from among halogeno, C1-C6 alkyl, hydroxyl, mercapto, amino and so on.</p>
申请公布号 WO0100641(A1) 申请公布日期 2001.01.04
申请号 WO2000JP04092 申请日期 2000.06.22
申请人 SANKYO COMPANY, LIMITED;IMANISHI, TAKESHI;KOHIGA, SATOSHI 发明人 IMANISHI, TAKESHI;KOHIGA, SATOSHI
分类号 C07H19/06;C07H19/10;C07H19/16;C07H19/20;(IPC1-7):C07H19/06;C07H21/00 主分类号 C07H19/06
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