Pravdina N F, Papchikhin A V, Purygin P P, Galegov G A
Mol Gen Mikrobiol Virusol. 1989 Jan(1):29-33.
Some new analogues of ribonucleoside-5'-triphosphates modified in 3'-ribose position and base [CTP (3'NH2), CTP (3'NH2) (5Me), CTP (3'N3) (5 Me), RvTP (3'N3)] have been synthesized. The inhibitions of RNA-synthesis catalyzed by the influenza A viral RNA-polymerase in cell free system and by the RNA-polymerase II from mice liver in the system of cellular nuclei by these reagents have been compared. All the studied preparations efficiently inhibited the RNA-synthesis in both cases. The inhibitors modified only in 3'-ribose position did not express specificity to any of RNA-polymerases tested, while some analogues having two modification in the molecule demonstrated the selective inhibition of RNA-synthesis directed by the influenza A viral RNA-polymerase [ara GTP (3'NH2), RvTP (3'N3')].
已合成了一些在3'-核糖位置和碱基上修饰的核糖核苷-5'-三磷酸的新类似物[CTP(3'NH2)、CTP(3'NH2)(5Me)、CTP(3'N3)(5Me)、RvTP(3'N3)]。比较了这些试剂在无细胞体系中对甲型流感病毒RNA聚合酶催化的RNA合成以及在细胞核体系中对小鼠肝脏RNA聚合酶II的抑制作用。所有研究的制剂在两种情况下均有效抑制RNA合成。仅在3'-核糖位置修饰的抑制剂对所测试的任何一种RNA聚合酶均无特异性表达,而分子中有两种修饰的一些类似物表现出对甲型流感病毒RNA聚合酶指导的RNA合成的选择性抑制作用[ara GTP(3'NH2)、RvTP(3'N3')]。