Benencia F, Courrèges M C
Departamento Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón II, Piso 4, Ciudad Universitaria, (1428) Buenos Aires, Argentina.
Phytother Res. 2000 Nov;14(7):495-500. doi: 10.1002/1099-1573(200011)14:7<495::aid-ptr650>3.0.co;2-8.
Eugenol (4-allyl-1-hydroxy-2-methoxybenzene) was tested for antiviral activity against HSV-1 and HSV-2 viruses. In vitro, it was found that the replication of these viruses was inhibited in the presence of this compound. Inhibitory concentration 50% values for the anti-HSV effects of eugenol were 25.6 microg/mL and 16.2 microg/mL for HSV-1 and HSV-2 respectively, 250 microg/mL being the maximum dose at which cytotoxicity was tested. Eugenol was virucidal and showed no cytotoxicity at the concentrations tested. Eugenol-acyclovir combinations synergistically inhibited herpesvirus replication in vitro. Topical application of eugenol delayed the development of herpesvirus induced keratitis in the mouse model.
对丁香酚(4-烯丙基-1-羟基-2-甲氧基苯)针对单纯疱疹病毒1型(HSV-1)和单纯疱疹病毒2型(HSV-2)的抗病毒活性进行了测试。在体外实验中发现,在该化合物存在的情况下,这些病毒的复制受到抑制。丁香酚抗HSV作用的半数抑制浓度值,对于HSV-1和HSV-2分别为25.6微克/毫升和16.2微克/毫升,250微克/毫升为测试细胞毒性的最大剂量。丁香酚具有杀病毒作用,在所测试的浓度下未显示出细胞毒性。丁香酚-阿昔洛韦组合在体外协同抑制疱疹病毒复制。在小鼠模型中,丁香酚的局部应用延缓了疱疹病毒诱导的角膜炎的发展。