发明名称 2′-fluoronucleoside phosphonates as antiviral agents
摘要 The present invention includes compounds and compositions of ®-2′-fluoronucleoside phosphonates, as well as methods to treat HIV, HBV, HCV or abnormal cellular proliferation comprising administering said compounds or compositions.
申请公布号 US8895531(B2) 申请公布日期 2014.11.25
申请号 US200711726686 申请日期 2007.03.22
申请人 RFS Pharma LLC 发明人 Shi Junxing
分类号 A61K31/70;C07H17/04;C07H19/10;C07H19/06;C07H19/04;C07H19/20;C07H19/16;C07F9/6561;C07F9/6558 主分类号 A61K31/70
代理机构 代理人 Bradin David
主权项 1. A compound having a structure consistent with formula (1) or a pharmaceutically acceptable salt thereof, wherein: a) X is O, S, SO2, or CH2; b) n is 1 or 2; c) R1 is CH3; d) R2 and R3 are independently a hydrogen, halogen, OH, OR′, SH, SR′, N3, NH2, NHR′, CN, OCOR′, OCOOR′, lower alkyl of C1-C6, halogenated lower alkyl of C1-C6, lower alkenyl of C2-C6, halogenated lower alkenyl of C2-C6, lower alkynyl of C2-C6, halogenated lower alkynyl of C2-C6, lower alkoxy of C1-C6 lower alkyl acid of C2-C6, or lower alkyl acid ester of C2-C6; e) each R′ is independently a hydrogen, lower alkyl of C1-C6, or lower cycloalkyl of C1-C6; f) R4 and R5 are independently a hydrogen, phosphate, diphosphate, or analogs thereof wherein one or two hydrogens on a P(OH) moiety is replaced with an C1-10 alkyl, aryl, amino acid ester, steroid, carbohydrate, or lipid group, wherein aryl groups are selected from the group consisting of phenyl, biphenyl, and naphthyl, optionally substituted with one or more moieties selected from the group consisting of hydroxyl, amino, alkylamino, arylamino, alkoxy, aryloxy, nitro, cyano, sulfonic acid, sulfate, phosphonic acid, phosphate, and phosphonate, and g) Base is a heterocycle containing at least one nitrogen.
地址 Tucker GA US