Renard-Nozaki J, Kim T, Imakura Y, Kihara M, Kobayashi S
Department of Microbiology, Tokyo Medical College, Japan.
Res Virol. 1989 Mar-Apr;140(2):115-28. doi: 10.1016/s0923-2516(89)80089-5.
Studies were carried out on the effects of Amaryllidaceae alkaloids and their derivatives upon herpes simplex virus (type 1), the relationship between their structure and antiviral activity and the mechanism of this activity. All alkaloids used in these experiments were biosynthesized from N-benzylphenethylamine; the apogalanthamine group was synthesized in our laboratory; those which may eventually prove to be antiviral agents had a hexahydroindole ring with two functional hydroxyl groups. Benzazepine compounds were neither cytotoxic nor antiviral, but many structures containing dibenzazocine were toxic at low concentrations. It was established that the antiviral activity of alkaloids is due to the inhibition of multiplication and not to the direct inactivation of extracellular viruses. The mechanism of the antiviral effect could be partly explained as a blocking of viral DNA polymerase activity.
开展了关于石蒜科生物碱及其衍生物对单纯疱疹病毒(1型)的影响、其结构与抗病毒活性之间的关系以及这种活性机制的研究。这些实验中使用的所有生物碱均由N - 苄基苯乙胺生物合成;阿扑加兰他敏类化合物是在我们实验室合成的;那些最终可能被证明是抗病毒剂的化合物具有带有两个功能性羟基的六氢吲哚环。苯并氮杂䓬化合物既无细胞毒性也无抗病毒活性,但许多含有二苯并氮杂辛的结构在低浓度下具有毒性。已确定生物碱的抗病毒活性是由于抑制增殖,而非直接使细胞外病毒失活。抗病毒作用的机制部分可解释为对病毒DNA聚合酶活性的阻断。