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作为抗植物病毒剂的嘧啶碱基前体类似物。

Analogues of pyrimidine base precursors as antiphytoviral agents.

作者信息

Schuster G, Arenhövel C, Golovinsky E

出版信息

Antiviral Res. 1987 Mar;7(3):179-84. doi: 10.1016/0166-3542(87)90006-4.

Abstract

Dihydroorotic acid hydrazide (DHOH) did not inhibit the replication of potatovirus X (PVX) in leaf disks of Nicotiana tabacum 'Samsun'. In contrast, 5-fluoroorotic acid (5-FOA) completely inhibited the replication of PVX, as demonstrated by a serological virus assay as well as a local lesion bioassay using Gomphrena globosa as the test plant. The corresponding base analogue 5-fluorouracil (5-FU) had only a weak inhibitory effect. Time-course inhibition experiments in synchronized virus-infected leaf disks led us to conclude that 5-FOA, as well as 5-azadihydrouracil (5-ADHU), an uracil catabolite analogue, inhibit the same early event in virus infection. Neither 5-FOA nor 5-ADHU had a direct inactivating effect on free PVX virions.

摘要

二氢乳清酸酰肼(DHOH)不会抑制烟草“三生烟”叶圆片中马铃薯X病毒(PVX)的复制。相比之下,5-氟乳清酸(5-FOA)完全抑制了PVX的复制,这通过血清学病毒检测以及使用千日红作为试验植物的局部病斑生物测定得到了证实。相应的碱基类似物5-氟尿嘧啶(5-FU)只有微弱的抑制作用。在同步病毒感染的叶圆片中进行的时间进程抑制实验使我们得出结论,5-FOA以及尿嘧啶分解代谢物类似物5-氮杂二氢尿嘧啶(5-ADHU)在病毒感染中抑制相同的早期事件。5-FOA和5-ADHU对游离的PVX病毒粒子均无直接灭活作用。

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