Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/1468
Title: (-)-Epigallocatechin gallate derivatives for inhibiting proteasome
Authors: Chan, TH 
Lam, WH
Chow, LMC 
Dou, QP
Kuhn, DJ
Kazi, A
Keywords: Catechin
Anticancer agent
Issue Date: 9-Jun-2009
Source: US Patent 7,544,816 B2. Washington, DC: US Patent and Trademark Office, 2009. How to cite?
Abstract: (-)-EGCG, the most abundant catechin, was found to be chemopreventive and anticancer agent. However, (-)-EGCG has at least one limitation: it gives poor bioavailability. This invention provides compounds of generally formula 10, wherein R₁ is selected from the group of --H and C₁ to C[sub 6] acyl group; R₂, R₃, and R₄ are each independently selected from the group of --H, --OH, and C₁ to C[sub 6] acyloxyl group; and at least one of R₂, R₃, or R₄ is --H. The derivatives of (-)-EGCG that is at least as potent as (-)-EGCG. The carboxylate protected forms of (-)-EGCG and its derivatives are found to be more stable than the unprotected forms, which can be used as proteasome inhibitors to reduce tumor cell growth.
URI: http://hdl.handle.net/10397/1468
Rights: Assignee: The Hong Kong Polytechnic University.
Assignee: Wayne State University.
Assignee: University of South Florida.
Assignee: McGill University.
Appears in Collections:Patent

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