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Review
. 2018 Feb 23;23(2):480.
doi: 10.3390/molecules23020480.

Sulphated Flavonoids: Biosynthesis, Structures, and Biological Activities

Affiliations
Review

Sulphated Flavonoids: Biosynthesis, Structures, and Biological Activities

Yanna C F Teles et al. Molecules. .

Abstract

The great diversity of enzymatic reactions in plant secondary metabolism allows the continuous discovery of new natural compounds and derivatives. Flavonoids, for example, can be found as aglycone or as several sorts of glycosylated, acetylated, methylated, and sulphated derivatives. This review focuses on sulphated flavonoids, an uncommon group of flavonoid derivatives found in some plant families. This work presents a compilation of sulphated flavonoids and their natural sources reported in the literature. Biosynthetic aspects and biological activities have also been reviewed, showing that these particular kinds of natural compounds play an interesting role in plant metabolism, as well as being potential candidates for the development of new drugs.

Keywords: secondary metabolism; sulphated flavonoids; sulphation; sulphotransferases.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flavonoid characteristic skeleton and known flavonoids.
Figure 2
Figure 2
Chalcone isomerization to form a flavanone.
Figure 3
Figure 3
Structure of Persicarin, the first sulphated flavonoid reported.

References

    1. Weng J.K., Philippe R.N., Noel J.P. The rise of chemodiversity in plants. Science. 2012;336:1667–1670. doi: 10.1126/science.1217411. - DOI - PubMed
    1. Li D., Heiling S., Baldwin I.T., Gaquerel E. Illuminating a plant’s tissue-specific metabolic diversity using computational metabolomics and information theory. Proc. Natl. Acad. Sci. USA. 2016;113:E7610–E7618. doi: 10.1073/pnas.1610218113. - DOI - PMC - PubMed
    1. Gandhi S.G., Mahajan V., Bedi Y.S. Changing trends in biotechnology of secondary metabolism in medicinal and aromatic plants. Planta. 2015;241:303–317. doi: 10.1007/s00425-014-2232-x. - DOI - PubMed
    1. Tsao R. Chemistry and biochemistry of dietary polyphenols. Nutrients. 2010;2:1231–1246. doi: 10.3390/nu2121231. - DOI - PMC - PubMed
    1. Mierziak J., Kostyn K., Kulma A. Flavonoids as Important Molecules of Plant Interactions with the Environment. Molecules. 2014;19:16240–16265. doi: 10.3390/molecules191016240. - DOI - PMC - PubMed

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