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ID: ALA1141592

Journal: Bioorg Med Chem Lett

Title: Synthesis and anti-inflammatory activities of mono-carbonyl analogues of curcumin.

Authors: Liang G, Li X, Chen L, Yang S, Wu X, Studer E, Gurley E, Hylemon PB, Ye F, Li Y, Zhou H.

Abstract: Curcumin has been extensively studied for its anti-inflammatory activities. However, its potential beneficial effects on various disease preventions and treatments are limited by its unstable structure. The beta-diketone moiety renders curcumin to be rapidly metabolized by aldo-keto reductase in liver. In the present study, a series of curcumin analogues with more stable chemical structures were synthesized and several compounds showed an enhanced ability to inhibit lipopolysaccharide (LPS)-induced TNF-alpha and IL-6 synthesis in macrophages.

CiteXplore: 18234497

DOI: 10.1016/j.bmcl.2007.12.068