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- W2902978830 abstract "Diarylheptanoids are a family of plant secondary metabolites with a 7 carbon skeleton possessing two phenyl rings at the 1- and 7-positions. They can be subdivided into acyclic and cyclic diarylheptanoids where the latter are further divided into meta,meta-bridged biphenyls ([7.0]metacyclophanes) and meta,para-bridged diphenyl ether heptanoids (oxa[7.1]metapara-cyclophanes). Since the isolation of curcumin from the rhizomes of turmeric (Curcuma longa) in 1815 which was named curcumin, a variety of diarylheptanoids have been isolated from a number of plant families such as Aceraceae, Actinidiaceae, Betulaceae, Burseraceae, Casuarinaceae, Juglandaceae, Leguminosae, Myricaceae, and Zingiberaceae. Earlier studies on these diarylheptanoids have been summarized on several occasions, of which the main themes only focus on isolation, structure elucidation, and the biological properties of linear types. Only a few have covered cyclic diarylheptanoids and their chemical synthesis has been covered lastly by Zhu et al. in 2000. The present paper has, therefore, covered recent progress in cyclic diarylheptanoids focusing on the isolation, structural and biological features, and chemical synthesis." @default.
- W2902978830 created "2018-12-11" @default.
- W2902978830 creator A5045383471 @default.
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- W2902978830 date "2018-11-27" @default.
- W2902978830 modified "2023-10-16" @default.
- W2902978830 title "Recent Studies on Cyclic 1,7-Diarylheptanoids: Their Isolation, Structures, Biological Activities, and Chemical Synthesis" @default.
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- W2902978830 doi "https://doi.org/10.3390/molecules23123107" @default.
- W2902978830 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6321387" @default.
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- W2902978830 hasPublicationYear "2018" @default.
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