Thiourea inhibitors of herpesviruses. Part 3: Inhibitors of varicella zoster virus
摘要:
The preparation of alpha-methylbenzyl thioureas and their biological activity against varicella zoster virus is described. Several analogs demonstrated IC(50)s < 0.1 muM and their SAR are discussed. These compounds represent a novel class of potent and selective nonnucleoside inhibitors of varicella zoster virus. (C) 2004 Elsevier Ltd. All rights reserved.
Thiourea inhibitors of herpesviruses. Part 3: Inhibitors of varicella zoster virus
摘要:
The preparation of alpha-methylbenzyl thioureas and their biological activity against varicella zoster virus is described. Several analogs demonstrated IC(50)s < 0.1 muM and their SAR are discussed. These compounds represent a novel class of potent and selective nonnucleoside inhibitors of varicella zoster virus. (C) 2004 Elsevier Ltd. All rights reserved.
[EN] SUBSTITUTED P-DIAMINOBENZENE DERIVATIVES<br/>[FR] DERIVES DE PARA-DIAMINOBENZENE SUBSTITUES
申请人:LUNDBECK & CO AS H
公开号:WO2004082677A1
公开(公告)日:2004-09-30
The present invention relates to aniline derivatives of the general formula I or pharmaceutically acceptable salts thereof and their use.
本发明涉及通式I的苯胺衍生物或其药学上可接受的盐及其用途。
Substituted p-diaminobenzene derivatives
申请人:Khanzhin Nikolay
公开号:US20060183791A1
公开(公告)日:2006-08-17
The present invention relates to aniline derivatives of the general formula I or pharmaceutically acceptable salts thereof and their use.
本发明涉及一般式I的苯胺衍生物或其药学上可接受的盐及其用途。
EP1613303A1
申请人:——
公开号:EP1613303A1
公开(公告)日:2006-01-11
US7906537B2
申请人:——
公开号:US7906537B2
公开(公告)日:2011-03-15
Thiourea inhibitors of herpesviruses. Part 3: Inhibitors of varicella zoster virus
作者:Martin J Di Grandi、Kevin J Curran、Gregg Feigelson、Amar Prashad、Adma A Ross、Robert Visalli、Jeanette Fairhurst、Boris Feld、Jonathan D Bloom
DOI:10.1016/j.bmcl.2004.06.025
日期:2004.8
The preparation of alpha-methylbenzyl thioureas and their biological activity against varicella zoster virus is described. Several analogs demonstrated IC(50)s < 0.1 muM and their SAR are discussed. These compounds represent a novel class of potent and selective nonnucleoside inhibitors of varicella zoster virus. (C) 2004 Elsevier Ltd. All rights reserved.