Synthesis and Antiviral Activity of Novel 1,3,4-Thiadiazine Derivatives

抄録

A series of novel 1,3,4-thiadiazine derivatives were synthesized via chemical optimization on phthiobuzone. Their anti-herpes simplex virus (HSV) activities in vitro were also tested. Several compounds exhibited more highly potent anti-HSV activity and much higher selectivity index (SI) values than those of phthiobuzone. The most potent anti-HSV compound was 4f, which showed marked inhibition against HSV-1 (IC₅₀=77.04 μg/ml) and HSV-2 (IC₅₀=30.00 μg/ml). Meanwhile it had low cytotoxicity (CC₅₀=1000.00 μg/ml), resulting in high (SI_HSV-1=12.98, SI_HSV-2=33.33, respectively). Furthermore, a computational study for prediction of absorption, distribution, metabolism, excretion (ADME) properties of compound 4f was performed by determination of topological polar surface area, absorption and Lipinski parameters.