Rollinson E A, White G
Antimicrob Agents Chemother. 1983 Aug;24(2):221-6. doi: 10.1128/AAC.24.2.221.
Compound BW759 (9-[2-hydroxy-1-(hydroxymethyl)ethoxymethyl]guanine) was shown to be about 230 times more active than acyclovir (9-[2-hydroxyethoxymethyl]guanine) (ACV) against Equid herpesvirus type 1 infection in Syrian hamsters and was more effective against Aujeszky's disease in mice. The therapeutic superiority of BW759 over ACV was greater than expected from quantitative inhibitory results in tissue culture with these viruses. When administered to hamsters at dose rates sufficient to prevent any Equid herpesvirus type 1-induced mortality (100 mg of ACV per kg per day; 3 mg of BW759 per kg per day), BW759 inhibited viral multiplication, as judged by histopathological observations, clinical chemistry, and liver virus concentrations, to a greater extent than ACV. Compound BW759 was particularly effective when administered via the oral route. The reasons for the superiority of BW759 over ACV remain to be elucidated.
化合物BW759(9-[2-羟基-1-(羟甲基)乙氧基甲基]鸟嘌呤)在叙利亚仓鼠中对1型马疱疹病毒感染的活性比阿昔洛韦(9-[2-羟基乙氧基甲基]鸟嘌呤)(ACV)高约230倍,并且对小鼠的奥耶斯基氏病更有效。BW759相对于ACV的治疗优势大于根据这些病毒在组织培养中的定量抑制结果所预期的。当以足以预防任何1型马疱疹病毒引起的死亡的剂量率给仓鼠给药时(每天每千克100毫克ACV;每天每千克3毫克BW759),根据组织病理学观察、临床化学和肝脏病毒浓度判断,BW759比ACV更能抑制病毒增殖。化合物BW759经口服途径给药时特别有效。BW759优于ACV的原因尚待阐明。