Torney H L, Dulworth J K, Steward D L
Antimicrob Agents Chemother. 1982 Oct;22(4):635-8. doi: 10.1128/AAC.22.4.635.
A nitrobenzene derivative, MDL-860, was found to inhibit plaque formation, cytopathic effect, or both in 11 of 12 picornaviruses at concentrations which did not affect cell growth. The compound did not directly inactivate the virus. MDL-860 inhibited actinomycin D-resistant [3H]uridine uptake in cells infected with coxsackievirus A21 or rhinovirus 1-A, whereas incorporation into uninfected cells was not inhibited. With three picornaviruses (echovirus type 12, poliovirus type 2, and rhinovirus type 1-A) made photosensitive with neutral red, MDL-860 did not appear to cause a significant reduction in their loss of photosensitivity (uncoating) during the first 3 h of infection. MDL-860 appears to inhibit some early event in virus replication, after uncoating, which is required for synthesis of a majority of viral RNA.
一种硝基苯衍生物MDL - 860被发现,在不影响细胞生长的浓度下,能抑制12种微小核糖核酸病毒中11种病毒的斑块形成、细胞病变效应或两者兼具。该化合物不会直接使病毒失活。MDL - 860抑制了感染柯萨奇病毒A21或鼻病毒1 - A的细胞中对放线菌素D有抗性的[³H]尿苷摄取,而对未感染细胞的掺入没有抑制作用。对于三种用中性红使其光敏化的微小核糖核酸病毒(埃可病毒12型、脊髓灰质炎病毒2型和鼻病毒1 - A型),MDL - 860在感染的最初3小时内似乎并未导致其光敏性丧失(脱壳)显著降低。MDL - 860似乎在脱壳后抑制了病毒复制中的某些早期事件,而这些事件是大多数病毒RNA合成所必需的。