synthesis and biological activity of arylspiroborate salts derived from caffeic acid phenethyl ester

synthesis and biological activity of arylspiroborate salts derived from caffeic acid phenethyl ester

;Martin J. G. Hébert;Andrew J. Flewelling;Trevor N. Clark;Natalie A. Levesque;Jacques Jean-François;Marc E. Surette;Christopher A. Gray;Christopher M. Vogels;Mohamed Touaibia;Stephen A. Westcott
Journal of human genetics 2015 Vol. 2015 pp. -
135
hbert2015internationalsynthesis

Abstract

Two novel boron compounds containing caffeic acid phenethyl ester (CAPE) derivatives have been prepared and characterized fully. These new compounds and CAPE have been investigated for potential antioxidant and antimicrobial properties and their ability to inhibit 5-lipoxygenase and whether chelation to boron improves their biological activity. Sodium salt 4 was generally more active than ammonium salt 5 in the biological assays and surpassed the radical scavenging ability of CAPE. Compounds 4 and 5 were more active than CAPE and Zileuton in human polymorphonuclear leukocytes. These results clearly show the effectiveness of the synthesized salts as transporter of CAPE.

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181099
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10.1155/2015/418362
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