CAN Mediated oxidative addition of 2-hydroxynaphthoquinone to dienes: a facile synthesis of naphthofurandiones
摘要:
2-Hydroxy-1,4-naphthoquinone undergoes CAN mediated oxidative addition to various dienes followed by ring closure yielding corresponding furoquinones. (C) 2001 Elsevier Science Ltd. All rights reserved.
Methods of Treating Muscular Wasting Diseases Using NF-kB Activation Inhibitors
申请人:Guttridge C. Denis
公开号:US20070225315A1
公开(公告)日:2007-09-27
Methods for treating muscular wasting diseases such as Duchenne muscular dystrophy are disclosed. Specifically, the methods include administering to a subject in need of treatment for a muscular wasting disease, an NF-κB activation inhibitor capable of blocking the activation of NF-κB.
US8426355B2
申请人:——
公开号:US8426355B2
公开(公告)日:2013-04-23
US9173920B2
申请人:——
公开号:US9173920B2
公开(公告)日:2015-11-03
[EN] METHODS OF TREATING MUSCULAR WASTING DISEASES USING NF-KB ACTIVATION INHIBITORS<br/>[FR] MÉTHODES DE TRAITEMENT DES MALADIES D'ATROPHIE MUSCULAIRE AU MOYEN D'INHIBITEURS DE L'ACTIVATION DE NF-KB
申请人:THERALOGICS INC
公开号:WO2007106884A2
公开(公告)日:2007-09-20
[EN] Methods for treating muscular wasting diseases such as Duchenne muscular dystrophy are disclosed. Specifically, the methods include administering to a subject in need of treatment for a muscular wasting disease, an NF-KB activation inhibitor capable of blocking the activation of NF-KB. [FR] La présente invention concerne des méthodes de traitement des maladies d'atrophie musculaire telles que la dystrophie musculaire de Duchenne. De manière spécifique, ces méthodes consistent à administrer à un sujet nécessitant un tel traitement, un inhibiteur de l'activation de NF-KB capable de bloquer l'activation de NF-KB.
CAN Mediated oxidative addition of 2-hydroxynaphthoquinone to dienes: a facile synthesis of naphthofurandiones
作者:Vijay Nair、P.M Treesa、Davis Maliakal、Nigam P Rath
DOI:10.1016/s0040-4020(01)00700-1
日期:2001.9
2-Hydroxy-1,4-naphthoquinone undergoes CAN mediated oxidative addition to various dienes followed by ring closure yielding corresponding furoquinones. (C) 2001 Elsevier Science Ltd. All rights reserved.