Sidwell R W, Huffman J H, Call E W, Alaghamandan H, Cook P D, Robins R K
Antimicrob Agents Chemother. 1985 Sep;28(3):375-7. doi: 10.1128/AAC.28.3.375.
Activity of the new antiviral compound selenazofurin was compared with the known active compounds ribavirin and amantadine against influenza A and B viruses. In experiments with Madin Darby canine kidney cells, selenazofurin inhibited the cytopathic effect and yield of influenza A/NWS/33 virus, with 50% effective dose ranges of 0.7 to 1.4 micrograms/ml (virus rating [VR], 1.3 to 1.4). The 50% effective dose range for ribavirin was 1.2 to 1.6 micrograms/ml (VR, 1.0 to 1.3), and for amantadine it was 9 micrograms/ml (VR, 0.9). Selenazofurin and ribavirin were similarly inhibitory to influenza B/Lee/40 virus, whereas amantadine was inactive. Selenazofurin appeared somewhat cytotoxic in these studies at concentrations as low as 1 micrograms/ml.
将新型抗病毒化合物硒唑呋林与已知的活性化合物利巴韦林和金刚烷胺针对甲型和乙型流感病毒的活性进行了比较。在对马迪达比犬肾细胞进行的实验中,硒唑呋林抑制了甲型流感病毒A/NWS/33的细胞病变效应和产量,50%有效剂量范围为0.7至1.4微克/毫升(病毒评级[VR],1.3至1.4)。利巴韦林的50%有效剂量范围为1.2至1.6微克/毫升(VR,1.0至1.3),金刚烷胺的50%有效剂量范围为9微克/毫升(VR,0.9)。硒唑呋林和利巴韦林对乙型流感病毒B/Lee/40具有相似的抑制作用,而金刚烷胺则无活性。在这些研究中,硒唑呋林在低至1微克/毫升的浓度下似乎具有一定的细胞毒性。