Suppression of proliferation of poliovirus and porcine parvovirus by novel phenoxazines, 2-amino-4,4α-dihydro-4α-7-dimethyl-3H-phenoxazine-3-one and 3-amino-1,4α-dihydro-4α-8-dimethyl-2H-phenoxazine-2-one

被引:15
作者
Iwata, A
Yamaguchi, T
Sato, K
Yoshitake, N
Tomoda, A
机构
[1] Tokyo Med Univ, Dept Biochem, Tokyo 1600022, Japan
[2] Tokyo Med Univ, Intractable Immune Syst Dis Res Ctr, Tokyo 1600022, Japan
[3] Natl Inst Hlth, Div Cellular & Gene Therapy Prod, Setagaya Ku, Tokyo 1580098, Japan
[4] Inst Saitama Red Cross Cente, Kamiochiai, Saitama 3380001, Japan
[5] Tokyo Med Univ, Dept Internal Med 3, Tokyo 1600022, Japan
关键词
phenoxazine; poliovirus; porcine parvovirus;
D O I
10.1248/bpb.28.905
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study aimed at investigating the antiviral effects of 2-amino-4,4 alpha-dihydro-4 alpha-7-dimethyl-3Hphenoxazine-3-one (Phx-1) and 3-amino-1,4 alpha-dihydro-4 alpha-8-dimethyl-2H-phenoxazine-2-one (Phx-2) on 6 representative viruses: poliovirus, porcine parvovirus, simian virus 40 (SV-40), herpes simplex virus-1 (HSV-1), Sindbis virus, and vesicular stornatitis virus (VSV). Phx-1 and Phx-2 suppressed the proliferation of poliovirus in Vero cells and that of porcine parvovirus in ESK cells at concentrations between 0.25 mu g/ml and 2 mu g/ml, when the cells were treated with Phx-1 and Phx-2 for I h and then inoculated with these viruses. The proliferation of the other viruses, SV-40, HSV-1, Sindbis virus, and VSV, in the host cells was not influenced by Phx-1 or Phx-2 at concentrations less than 20 mu g/ml. The results suggest that Phx-1 and Phx-2 may be useful to prevent the proliferation of poliovirus and porcine parvovirus infection and may contribute to developing new antiviral drugs in future.
引用
收藏
页码:905 / 907
页数:3
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