Sugita K, Arita H, Kawanami J, Sato K
J Gen Virol. 1979 Oct;45(1):249-51. doi: 10.1099/0022-1317-45-1-249.
The antiviral activity of phenyl-6-chloro-6-deoxy-beta-D-glucopyranoside (PCG) was studied. PCG specifically inhibited the growth of paramyxoviruses including Sendai, measles and Newcastle disease viruses in LLCMK2 cells at a concentration of 0.5 to 1.0 mM, but did not restrict the multiplication of other RNA viruses (influenza, vesicular stomatitis and polio viruses) at these concentrations. PCG might act in the late stage during virus replication of Sendai virus as it did not inhibit virus RNA and protein synthesis in the infected cells. Comparative studies on the biological properties of virus particles grown in the presence and absence of PCG demonstrated that treatment with it caused the formation of non-haemagglutinating particles.
研究了苯基-6-氯-6-脱氧-β-D-吡喃葡萄糖苷(PCG)的抗病毒活性。PCG在浓度为0.5至1.0 mM时,可特异性抑制包括仙台病毒、麻疹病毒和新城疫病毒在内的副粘病毒在LLCMK2细胞中的生长,但在这些浓度下并不限制其他RNA病毒(流感病毒、水泡性口炎病毒和脊髓灰质炎病毒)的增殖。PCG可能在仙台病毒复制的后期起作用,因为它不抑制受感染细胞中的病毒RNA和蛋白质合成。对在有和没有PCG的情况下生长的病毒颗粒的生物学特性进行的比较研究表明,用PCG处理会导致形成非血凝性颗粒。