发明名称 2'-Fluoronucleosides
摘要 2'-Fluoronucleoside compounds are disclosed which are useful in the treatment of hepatitis B infection, hepatitis C infection, HIV and abnormal cellular proliferation, including tumors and cancer. The compounds have general formulae (I), (II), (III), (IV) wherein Base is a purine or pyrimidine base; R 1 is OH, H, OR 3 , N 3 , CN, halogen, including F, or CF 3 , lower alkyl, amino, loweralkylamino, di(lower)alkylamino, or alkoxy, and base refers to a purine or pyrimidine base; R 2 is H, phosphate, including monophosphate, diphosphate, triphosphate, or a stabilized phosphate prodrug; acyl, or other pharmaceutically acceptable leaving group which when administered in vivo, is capable of providing a compound wherein R 2 is H or phosphate; sulfonate ester including alkyl or arylalkyl sulfonyl including methanesulfonyl, benzyl, wherein the phenyl group is optionally substituted with one or more substituents as described in the definition of aryl given above, a lipid, an amino acid, peptide, or cholesterol; and R 3 is acyl, alkyl, phosphate, or other pharmaceutically acceptable leaving group which when administered in vivo, is capable of being cleaved to the parent compound, or a pharmaceutically acceptable salt thereof.
申请公布号 KR100954390(B1) 申请公布日期 2010.04.26
申请号 KR20097000710 申请日期 1999.02.25
申请人 发明人
分类号 C07D239/47;C07H19/06;A61K31/505;A61K31/506;A61K31/52;A61K31/522;A61K31/7042;A61K31/7052;A61K31/7064;A61K31/7068;A61K31/7072;A61K31/7076;A61K31/708;A61P31/12;A61P31/20;A61P35/00;C07D405/04;C07D473/00;C07D473/18;C07D473/34;C07F7/18;C07F9/547;C07H19/10;C07H19/16;C07H19/20;C07H19/207 主分类号 C07D239/47
代理机构 代理人
主权项
地址