Watanabe W, Sudo K, Sata R, Kajiyashiki T, Konno K, Shigeta S, Yokota T
Rational Drug Design Laboratories, Fukushima, Japan.
Biochem Biophys Res Commun. 1998 Aug 28;249(3):922-6. doi: 10.1006/bbrc.1998.9222.
Benzodithiin derivatives are highly potent and specific inhibitors of respiratory syncytial virus (RSV) replication in vitro. The most potent and selective congener of a benzodithiin derivative is 1,4-dihydro-2,3-benzodithiin(RD3-0028). According to the modified 3-(4,5-dimethylthiazole-2-yl) 2,5-diphenyl tetrazolium bromide (MTT) assay developed in our laboratories, this compound has a 50% effective concentration of 4.5 microM and a 50% cytotoxic concentration of 271.0 microM, which is superior to that of ribavirin. This compound also inhibits RSV strain subgroups A and B and clinical isolates. RD3-0028, however, does not inhibit the replication of influenza A virus, measles virus, herpes simplex virus types 1 and 2, or human cytomegalovirus. Two other benzodithiin derivatives [1,4-dihydro-6-methyl-2,3-benzodithiin (RD3-0270) and 1,4-dihydro-5-methyl-1-2,3-benzodithiin (RD3-0284)] also inhibit RSV replication at a selectivity index greater a factor of 20. These results suggest that the benzodithiin skeleton is an important structure for inhibitory activity against RSV replication.
苯并二硫醚衍生物在体外是呼吸道合胞病毒(RSV)复制的高效且特异性抑制剂。苯并二硫醚衍生物中最具活性和选择性的同系物是1,4-二氢-2,3-苯并二硫醚(RD3-0028)。根据我们实验室开发的改良3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)测定法,该化合物的50%有效浓度为4.5微摩尔,50%细胞毒性浓度为271.0微摩尔,优于利巴韦林。该化合物还可抑制RSV A组和B组毒株以及临床分离株。然而,RD3-0028不抑制甲型流感病毒、麻疹病毒、1型和2型单纯疱疹病毒或人巨细胞病毒的复制。另外两种苯并二硫醚衍生物[1,4-二氢-6-甲基-2,3-苯并二硫醚(RD3-0270)和1,4-二氢-5-甲基-1-2,3-苯并二硫醚(RD3-0284)]也以大于20的选择性指数抑制RSV复制。这些结果表明,苯并二硫醚骨架是对RSV复制具有抑制活性的重要结构。