发明名称 ANTIVIRAL COMPOUNDS AND METHODS OF USE THEREOF
摘要 Inhibitors of retroviral propagation, methods of treatment and prevention of retroviral infections using the inhibitors, and pharmaceutical compositions including the inhibitors, are disclosed.
申请公布号 US2015359786(A1) 申请公布日期 2015.12.17
申请号 US201414761503 申请日期 2014.01.17
申请人 TRANA DISCOVERY, INC. 发明人 Guenther Richard H.;Sternbach Daniel;Peterson Steven E.
分类号 A61K31/47;A61K31/366;A61K45/06 主分类号 A61K31/47
代理机构 代理人
主权项 1. A pharmaceutical composition comprising a compound of the following formulas:wherein: R is selected from the group consisting of hydrogen, lower alkyl (C1-C6), lower haloalkyl (C1-C6), lower alkoxy (C1-C6), lower alkenyl (C2-C6), lower alkynyl (C2-C6), lower cycloalkyl (C3-C6) aryl, heteroaryl, heterocyclic, alkylaryl, arylalkyl, hydroxyl, nitro, cyano, cyanoalkyl, azido, azidoalkyl, formyl, hydrazino, halo, OR′, N(R′)2, SR′, COOR′, COR′, OCOR′, NHCOR′, N(COR′)COR′, SCOR′, OCOOR′, and NHCOOR′, wherein each R′ is independently H, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, aryl, heteroaryl, alkylaryl, or arylalkyl, wherein the groups can be substituted with one or more substituents as defined above, R1 is selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C126 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, aryl, heteroaryl, heterocyclic, alkylaryl, and arylalkyl, R2 is selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, aryl, heteroaryl, heterocyclic, alkylaryl, arylalkyl, hydroxyl, nitro, cyano, cyanoalkyl, azido, azidoalkyl, formyl, hydrazino, halo, OR′, N(R′)2, SR′, COOR′, COR′, OCOR′, NHCOR′, N(COR′)COR′, SCOR′, OCOOR′, and NHCOOR′, wherein each R′ is independently H, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, aryl, heteroaryl, alkylaryl, or arylalkyl R3 and R4, are, independently, the same or different, and are selected from the group consisting of hydrogen and C1-6 alkyl, R5 is —OR6, —NHR6, —CH2R6, or —CH2CH2R6, R6=—CH2CO2H, —CH2NR3R4, phenyl (“Ph”), or PhR (wherein the R moiety is ortho, meta, or para to the —O, —NH, —CH2, or —CH2CH2 moiety attached to the phenyl substituent in R5), n is 0, 1, or 2, and X is NR′, 0, S, Se, or CR2, and pharmaceutically acceptable salts thereof.
地址 Cary NC US