Shneĭder M A, Shtil'bans E B, Rachkovskaia L A, Poltorak V A
Antibiotiki. 1983 May;28(5):352-7.
Clear antiviral activity of carbonyl-conjugated pentaene macrolides, such as flavofungin, mycothicin, brunefungin and flavopentin was shown on models with infectious and oncogenic viruses. The antibiotics were active against influenza A and B virus. The effect was most pronounced in the in vitro and in ovo systems. On a model of experimental influenza infection of mice with the lethal outcome, antiinfluenzal activity of flavofungin was comparable to that of remantadin. However, unlike the latter one flavofungin and brunefungin inhibited the growth of influenza B virus. The drugs had a pronounced inhibitory effect on variolavaccine virus and prevented formation of foci of cell neoplastic transformation infected with various strains of Rous sarcoma virus.
羰基共轭戊二烯大环内酯类抗生素,如黄霉素、霉菌素、棕曲菌素和黄戊菌素,在感染性和致癌性病毒模型上显示出明显的抗病毒活性。这些抗生素对甲型和乙型流感病毒具有活性。在体外和卵内系统中,这种效果最为显著。在小鼠实验性流感感染致死模型中,黄霉素的抗流感活性与金刚烷胺相当。然而,与后者不同的是,黄霉素和棕曲菌素能抑制乙型流感病毒的生长。这些药物对牛痘疫苗病毒有显著的抑制作用,并能阻止感染各种劳斯肉瘤病毒株的细胞发生肿瘤转化灶的形成。