[EN] DIPHENYLUREA DERIVATIVES AND THEIR USE AS CHLORIDE CHANNEL BLOCKERS<br/>[FR] DERIVES DE DIPHENYLUREE ET LEUR UTILISATION EN TANT QUE BLOQUANTS DE CANAUX CHLORURE
申请人:NEUROSEARCH AS
公开号:WO2004111017A1
公开(公告)日:2004-12-23
The present invention relates to novel diphenylurea derivatives useful as chloride channel blockers. In other aspects the invention relates to the use of these compounds in a method for therapy, and to pharmaceutical compositions comprising the compounds of the invention.
Diphenylurea derivatives and their use as chloride channel blockers
申请人:Dahl H. Bjarne
公开号:US20060178413A1
公开(公告)日:2006-08-10
The present invention relates to novel diphenylurea derivatives useful as chloride channel blockers. In other aspects the invention relates to the use of these compounds in a method for therapy, and to pharmaceutical compositions comprising the compounds of the invention.
Diphenylurea Derivatives Useful As Potassium Channel Activators
申请人:Dahl H. Bjarne
公开号:US20070293553A1
公开(公告)日:2007-12-20
The present invention relates to the medical use of a certain group of diphenyl urea derivatives as potassium channel blockers for treating cardiovascular diseases, an obstructive or inflammatory airway disease, urinary incontinence, psychosis, epilepsy or pain, or for facilitating the blood-brain barrier permeability for other therapeutic substances. In other aspects the invention relates to the use of these compounds in a method of therapy.
NOVEL CINNAMIC AMIDE DERIVATIVES USEFUL AS ION CHANNEL MODULATORS
申请人:Nardi Antonio
公开号:US20100087496A1
公开(公告)日:2010-04-08
This invention relates to novel cinnamic amide derivatives that are found to be potent modulators of ion channels and, as such, they are valuable candidates for the treatment of diseases or disorders as diverse as those which are responsive to modulation of ion channels.
BETA-KETO-AMIDE DERIVATIVES USEFUL AS ION CHANNEL MODULATORS
申请人:Nardi Antonio
公开号:US20100137387A1
公开(公告)日:2010-06-03
This invention relates to novel β-keto-amide derivatives that are found to be potent modulators of ion channels, and in particular potassium channels and chloride channels, and, as such, are valuable candidates for the treatment of diseases or disorders as diverse as those which are responsive to the modulation of potassium channels.