作者:Yves Aubert、Marcel Chassignol、Victoria Roig、Gladys Mbemba、Julien Weiss、Hervé Meudal、Jean-François Mouscadet、Ulysse Asseline
DOI:10.1016/j.ejmech.2009.09.007
日期:2009.12
The synthesis of a series of thirty-eight new modified dinucleotides and dinucleotide conjugate analogues of d-5′ApC3′ is described. The inhibitory activity of these compounds toward HIV-1 integrase was examined in enzymatic assays using the natural dinucleotide as a reference. Among the compounds, a perylene-dinucleotide conjugate has shown a two micromolar anti-integrase activity due to the presence
一系列38新型改性二核苷酸和D-的二核苷酸偶联物类似物的合成5' APC 3'进行说明。这些酶对HIV-1整合酶的抑制活性在酶法测定中以天然二核苷酸为参考进行了检测。在这些化合物中,由于嵌入剂和二核苷酸的存在,a-二核苷酸缀合物具有两个微摩尔的抗整合酶活性。