发明名称 Use of SIRT1 activators or inhibitors to modulate an immune response
摘要 The present disclosure provides a method of increasing an immune response in an individual, the method involving administering to an individual in need thereof an inhibitor of SIRT1. The present disclosure provides a method of reducing an immune response, e.g., to treat chronic immune hyperactivity, the method generally involving administering to an individual in need thereof an activator of SIRT1. The present disclosure provides a method of modulating activation and differentiation of CD4+ T cells.
申请公布号 US8748464(B2) 申请公布日期 2014.06.10
申请号 US20100838247 申请日期 2010.07.16
申请人 The J. David Gladstone Institutes 发明人 Verdin Eric M.;Ott Melanie;Kwon Hye-Sook;Lim Hyungwook
分类号 A01N43/78;A61K31/535 主分类号 A01N43/78
代理机构 代理人
主权项 1. A method of treating chronic immune hyperactivity in an individual, the method comprising administering to an individual having chronic immune hyperactivity an effective amount of a SIRT1 activator, wherein the SIRT1 activator is a compound of the formula:or a salt thereof, wherein R19 is selected from:wherein: each Z10, Z11, Z12 and Z13 is independently selected from N, CR20 or CR1′; and each Z14, Z15 and Z16 is independently selected from N, NR1′, S, O, CR20, or CR1′, wherein: zero to two of Z10, Z11, Z12 or Z13 are N; at least one of Z14, Z15 and Z16 is N, NR1′, S or O; zero to one of Z14, Z15 and Z16 is S or O; zero to two of Z14, Z15 and Z16 is N or NR1′; zero to one R30 is a solubilizing group; and zero to one R1′ is an optionally substituted C1-C3 straight or branched alkyl; each R20 is independently selected from H or a solubilizing group; R21 is selected from —NR1′—C(O)—, —NR1′—S(O)2—, —NR1′—C(O)—NR1′—, —NR1′—C(S)—NR1′—NR1′—C(S)— NR1′—CR1′R1′—, —NR1′—C(O)—CR1′R1′—NR1′—, —NR1′—C(═NR1′)—NR1′—, —C(O)—NR1′—C(O)—NR1′—, —CR1′R1′—, —NR1′—C(O)—C(O)—CR1′═CR1′—, —NR1′—S(O)2—NR1′–—NR1′—C(O)—NR1′—S(O)2—, —NR1′—CR1′R1′—C(O)—NR1′—, —CR1′R1′—C(O)—NR1′—, —NR1′—C(O)—CR1′═CR1′—CR1′R1′—, —NR1′—C(═N—CN)—NR1′—, —NR1′—C(O)—CR1′R1′—O—, —NR1′—C(O)—CR1′R1—CR1′R1′—O—, —NR1′—S(O)2—CR1′R1′—, —NR1′—S(O)2—CR1′R1′—CR1′R1′—, —NR1′— C(O)—CR1′R1′—; —NR1′—C(O)—CR1′R′1—CR1′R′1—, —NR1′—C(S)—NR1′—CR1′R′1—CR1′R′1—, —NR1′—C(O)—O—,wherein each R1′ is independently selected from H or optionally substituted C1-C3 straight or branched alkyl; and R31 is selected from an optionally substituted monocyclic or bicyclic aryl, or an optionally substituted monocyclic or bicyclic heteroaryl,wherein the chronic immune hyperactivity results from an immunodeficiency virus infection.
地址 San Francisco CA US