Zerial A, Werner G H, Phillpotts R J, Willmann J S, Higgins P G, Tyrrell D A
Antimicrob Agents Chemother. 1985 May;27(5):846-50. doi: 10.1128/AAC.27.5.846.
A synthetic compound, 2-[(1,5,10,10a-tetrahydro-3H-thiazolo[3,4b]isoquinolin-3-ylidene) amino]-4-thiazoleacetic acid (S), 44 081 R.P., inhibits the multiplication of rhinoviruses in cell cultures. Of the 69 rhinovirus strains and serotypes that have been studied, 39% were inhibited at a concentration of 7 micrograms/ml, far below that which affects cellular metabolism (250 micrograms/ml). Preliminary data indicate that the compound inhibits some early events of virus replication but that some cellular functions are also involved in its mechanism of action. Despite its antiviral activity in vitro, the compound, when self-administered intranasally as a 0.2% solution to volunteers from the day before to 5 days after inoculation with a human rhinovirus strain, had no significant effect on rhinorrhea, clinical score, or laboratory evidence of infection.
一种合成化合物,2-[(1,5,10,10a-四氢-3H-噻唑并[3,4-b]异喹啉-3-亚基)氨基]-4-噻唑乙酸(S),44 081 R.P.,可抑制鼻病毒在细胞培养物中的增殖。在已研究的69种鼻病毒株和血清型中,39%在浓度为7微克/毫升时受到抑制,该浓度远低于影响细胞代谢的浓度(250微克/毫升)。初步数据表明,该化合物抑制病毒复制的一些早期事件,但某些细胞功能也参与其作用机制。尽管该化合物在体外具有抗病毒活性,但当以0.2%溶液从接种人鼻病毒株的前一天至接种后5天经鼻给志愿者自行给药时,对鼻漏、临床评分或感染的实验室证据均无显著影响。