Issue 3, 2019

Tautomerism and bioactivities of curcumenol, a common sesquiterpenoid widely existing in edible plants

Abstract

Curcumenol was firstly revealed as a pair of hemiacetal–ketone tautomers in solutions by using temperature variation 1H-NMR experiments, 2D NMR, and chemical methods. Quantum chemical calculation allowed the explanation of its spectroscopic behavior. An antioxidative SAR study on its derivatives verified the tautomeric bio-significance. Curcumenol also remarkably enhanced myogenic differentiation and mitochondrial function.

Graphical abstract: Tautomerism and bioactivities of curcumenol, a common sesquiterpenoid widely existing in edible plants

Supplementary files

Article information

Article type
Communication
Submitted
23 Dec 2018
Accepted
26 Feb 2019
First published
26 Feb 2019

Food Funct., 2019,10, 1288-1294

Tautomerism and bioactivities of curcumenol, a common sesquiterpenoid widely existing in edible plants

L. Zhang, S. Shen, Y. Gao, S. Shi, C. Zhou, J. Mo, Y. Xu, L. Lin and L. Gan, Food Funct., 2019, 10, 1288 DOI: 10.1039/C8FO02549E

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