Gallotannins and ellagitannins as regulators of cytokine release
申请人:The Penn State Research Foundation
公开号:US07288273B1
公开(公告)日:2007-10-30
A means and method for increasing or inhibiting the secretion of cytokines using gallotannins and ellagitannins is described. The preferred cytokine release inhibiting compounds are dimeric gallotannins having a linker molecule that misaligns the carbohydrate cores of the compounds. The preferred cytokine release promoting gallotannins and ellagitannins include a diaryl ether linker unit. In comparison to the more structurally complex ellagitannins, the compounds of this invention are structurally simpler, easier to synthesize, and more potent.
[EN] GALLOTANNINS AND ELLAGITANNINS AS REGULATORS OF CYTOKINE RELEASE<br/>[FR] GALLOTANIN ET ELLAGITANIN EN TANT QUE REGULATEURS DE LA LIBERATION DE CYTOKINES
申请人:PENN STATE RES FOUND
公开号:WO2001036436A1
公开(公告)日:2001-05-25
A means and method for increasing or inhibiting the secretion of cytokines using gallotannins and ellagitannins is described. The preferred cytokine release inhibiting compounds are dimeric gallotannins having a linker molecule that misaligns the carbohydrate cores of the compounds. The preferred cytokine release promoting gallotannins and ellagitannins include a diaryl ether linker unit. In comparison to the more structurally complex ellagitannins, the compounds of this invention are structurally simpler, easier to synthesize, and more potent.
GALLOTANNINS AND ELLIGITANNINS AS REGULATORS OF CYTOKINE RELEASE
申请人:FELDMAN KENNETH S.
公开号:US20080070850A1
公开(公告)日:2008-03-20
A means and method for increasing or inhibiting the secretion of cytokines using gallotannins and ellagitannins is described. The preferred cytokine release inhibiting compounds are dimeric gallotannins having a linker molecule that misaligns the carbohydrate cores of the compounds. The preferred cytokine release promoting gallotannins and ellagitannins include a diaryl ether linker unit. In comparison to the more structurally complex ellagitannins, the compounds of this invention are structurally simpler, easier to synthesize, and more potent.