| Literature DB >> 25442301 |
Armando Zarrelli1, Valeria Romanucci2, Concetta Tuccillo3, Alessandro Federico3, Carmela Loguercio3, Raffaele Gravante2, Giovanni Di Fabio1.
Abstract
New silibinin glyco-conjugates have been synthesized by efficient method and in short time. Exploiting our solution phase strategy, several structurally diverse silibinin glyco-conjugates (gluco, manno, galacto, and lacto-) were successfully realized in very good yields and in short time. In preliminary study to evaluate their antioxidant and neuroprotective activities new derivatives were subjected to DPPH free radical scavenging assay and the Xanthine oxidase (XO) inhibition models assay. Irrespective of the sugar moiety examined, new glyco-conjugates are more than 50 times water-soluble of silibinin. In the other hand they exhibit a radical scavenging activities slightly higher than to silibinin and XO inhibition at least as silibinin.Entities:
Keywords: Glyco-conjugates; Natural products; Phosphoramidite chemistry; Silibinin; Silybin
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Year: 2014 PMID: 25442301 DOI: 10.1016/j.bmcl.2014.10.023
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823