首页> 外国专利> HISTONE DEACETYLASE INHIBITOR THAT REACTIVATES HIV-1 PROVIRUSES FROM LATENTLY HIV-INFECTED CELLS

HISTONE DEACETYLASE INHIBITOR THAT REACTIVATES HIV-1 PROVIRUSES FROM LATENTLY HIV-INFECTED CELLS

机译:组蛋白去乙酰化酶抑制剂,可激活从最近感染了艾滋病毒的细胞中产生的HIV-1病毒

摘要

PURPOSE: A histone diacetylase(HDAC) inhibitor and a method for reactivating HIV-1 provirus are provided to ensure low cytotoxicity and high stability. CONSTITUTION: A histone diacetylase inhibitor of chemical formula 1 reactivates HIV-1 provirus from latent HIV infected cells. In chemical formula 1, R1 is independently C1-3 alkyl, hydroxy C1-2 alkyl, halo C1-2 alkyl, piperidinyl, morpholinyl, cyanomethyl, piperazinyl, di C1-2 alkylamino C1-2 alkyl, di C1-2 alkylamino C1-2 alkyl, piperidinyl C1-2 alkyl, morpholino C1-2 alkyl, or piperazino C1-2 alkyl; and R2 is hydrogen or methyl. The latent HIV infected cell is ACH2 cell or J1.1.
机译:目的:提供一种组蛋白二乙酰基酶(HDAC)抑制剂和一种HIV-1原病毒的活化方法,以确保低细胞毒性和高稳定性。组成:化学式1的组蛋白二乙酰酶抑制剂可从潜在的HIV感染细胞中重新激活HIV-1原病毒。在化学式1中,R 1独立地为C 1-3烷基,羟基C 1-2烷基,卤代C 1-2烷基,哌啶基,吗啉基,氰基甲基,哌嗪基,二C 1-2烷基氨基C 1-2烷基,二C 1-2烷基氨基C 1- 2个烷基,哌啶基C1-2烷基,吗啉代C1-2烷基或哌嗪子基C1-2烷基; R 2为氢或甲基。被HIV感染的潜伏细胞是ACH2细胞或J1.1。

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