| Literature DB >> 19939419 |
Kengo Shigetomi1, Kazuaki Shoji, Shinya Mitsuhashi, Makoto Ubukata.
Abstract
6-Tuliposide B is a secondary metabolite occurring specifically in tulip anthers. Recently, a potent antibacterial activity of 6-tuliposide B has been reported. However, its molecular target has not yet been established, nor its action mechanism. To shed light on such issues, 6-tuliposide B and tulipalin B analogues were synthesized and a structure-activity relationship (SAR) was examined using a broad panel of bacterial strains. As the results of SAR among a total of 25 compounds, only tulipalin B and the compounds having 3',4'-dihydroxy-2'-methylenebutanoate (DHMB) moieties showed any significant antibacterial activity. Moreover, the 3'R analogues of these compounds displayed essentially the same activities as 6-tuliposide B and the structure of the 3'R-DMBA moiety was the same as that of the proposed active moiety of cnicin. These results suggest that 6-tuliposide B has the same action mechanism as proposed for cnicin and bacterial MurA is one of the major molecular targets of 6-tuliposide B. 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 19939419 DOI: 10.1016/j.phytochem.2009.10.008
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072