Schleicher J B, Aquino F, Rueter A, Roderick W R, Appell R N
Appl Microbiol. 1972 Jan;23(1):113-6. doi: 10.1128/am.23.1.113-116.1972.
(S,S)-1,2-bis(5-methoxy-2-benzimidazolyl)-1,2-ethanediol showed antiviral activity in monolayer tissue culture systems against 55 strains of rhinovirus, three types of poliovirus, and strains of type A and B coxsackieviruses. Neither the compound nor any of the analogues tested showed virucidal activity. Its antiviral activity was not associated with interference with viral attachment to or penetration into the cell. At a concentration of 0.1 mg/ml, this group of compounds was generally nontoxic to WI-38, primary bovine kidney, and African green monkey kidney cells and had antiviral activity with 100% inhibition of virus-induced cytopathic effects (CPE). At antiviral levels, these compounds prevented CPE of up to 10(6) median tissue culture infective dose units of virus and completely inhibited formation of new infective virions. The compounds showed antiviral activity both prophylactically and therapeutically against rhinoviruses. Infected cultures could be cleared of CPE up to 90 hr after infection.
(S,S)-1,2-双(5-甲氧基-2-苯并咪唑基)-1,2-乙二醇在单层组织培养系统中对55株鼻病毒、三种脊髓灰质炎病毒以及甲型和乙型柯萨奇病毒毒株显示出抗病毒活性。所测试的该化合物及其任何类似物均未显示出杀病毒活性。其抗病毒活性与干扰病毒附着于细胞或穿透细胞无关。在浓度为0.1mg/ml时,这组化合物通常对WI-38细胞、原代牛肾细胞和非洲绿猴肾细胞无毒,并具有抗病毒活性,可100%抑制病毒诱导的细胞病变效应(CPE)。在抗病毒水平下,这些化合物可预防高达10⁶个半数组织培养感染剂量单位病毒的CPE,并完全抑制新的感染性病毒粒子的形成。这些化合物对鼻病毒在预防和治疗方面均显示出抗病毒活性。感染的培养物在感染后长达90小时内的CPE均可被清除。