INVITRO VIRUCIDAL ACTIVITY OF SELECTED ANTHRAQUINONES AND ANTHRAQUINONE DERIVATIVES

被引:145
作者
ANDERSEN, DO [1 ]
WEBER, ND [1 ]
WOOD, SG [1 ]
HUGHES, BG [1 ]
MURRAY, BK [1 ]
NORTH, JA [1 ]
机构
[1] MURDOCK HLTHCARE,DEPT RES & DEV,SPRINGVILLE,UT
关键词
ANTHRAQUINONE; HYPERICIN; EMODIN; VIRUCIDAL; TWEEN-80;
D O I
10.1016/0166-3542(91)90024-L
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Anthraquinones and anthraquinone derivatives were characterized for their antiviral and virucidal activities against viruses representing several taxonomic groups. One of these compounds, hypericin, had activity against vesicular stomatitis virus, herpes simplex virus types 1 and 2, parainfluenza virus, and vaccinia virus (from 0.5 to 3.8 log10 reductions in infectivity) at concentrations of less than 1-mu-g/ml as determined by a direct pre-infection incubation assay. Human rhinovirus was not sensitive to hypericin at concentrations up to 10-mu-g/ml. Addition of small amounts of Tween-80 to solutions containing hypericin enhanced, by up to 2.6 log10, hypericin's virucidal activity. Anthraquinones and anthraquinone derivatives with the hydroxyl and alkyl substitution pattern of emodin (i.e. emodin, emodin anthrone, emodin bianthrone and hypericin) were active against the enveloped viruses tested. The following general pattern of activity was found: hypericin > emodin bianthrone > emodin anthrone > emodin. Chrysophanic acid, aloe-emodin, and sennosides A and B did not possess activity against any of the viruses tested.
引用
收藏
页码:185 / 196
页数:12
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