TY - JOUR
T1 - 2-(2-phenylethyl)-4H-chromen-4-one derivatives from the resinous wood of Aquilaria sinensis with anti-inflammatory effects in LPS-induced macrophages
AU - Wang, Sin Ling
AU - Tsai, Yun Chen
AU - Fu, Shu Ling
AU - Cheng, Ming Jen
AU - Chung, Mei Ing
AU - Chen, Jih Jung
N1 - Publisher Copyright:
© 2018 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2018
Y1 - 2018
N2 - The resinous wood of Aquilaria sinensis, known as agarwood (Chen Xiang in Chinese), is traditionally used for the treatment of abdominal pain, vomiting, circulatory disorders, and dyspnea. Four new 2-(2-phenylethyl)-4H-chromen-4-one derivatives, namely 7-methoxy-2-[2-(40-hydroxyphenyl) ethyl]chromone (1), 7-hydroxy-2-[2-(40-methoxyphenyl)ethyl]chromone (2), 5,6-dihydroxy-2-[2-(30-hydroxy-40-methoxyphenyl)ethyl]chromone (3), and 6-hydroxy-5-methoxy-2-(2-phenylethyl) chromone (4), have been isolated from the resinous wood of A. sinensis, together with nine known compounds. The structures of these compounds were determined through spectroscopic and MS analyses. Among the isolated compounds, neopetasan, 7-methoxy-2-(2-phenylethyl)-chromone, 6,7-dimethoxy-2-(2-phenylethyl)chromone, and 6,7-dimethoxy-2-[2-(40-methoxyphenyl) ethyl]chromone inhibited NF-κB activation in LPS-stimulated RAW 264.7 macrophages with relative luciferase activity values of 0.55 ± 0.09, 0.54 ± 0.03, 0.31 ± 0.05, and 0.38 ± 0.14, respectively, versus that of vehicle control (1.03 ± 0.02). In addition, 5,6-dihydroxy-2-[2-(3'-hydroxy-4'-methoxyphenyl)ethyl]chromone, 7-methoxy-2-(2-phenylethyl)chromone, 7-dimethoxy-2-(2-phenylethyl)chromone, and 6,7-dimethoxy-2-[2-(4'-methoxyphenyl)ethyl]chromone could suppress LPS-induced NO production in RAW264.7 cells and did not induce cytotoxicity against RAW264.7 cells after 24-h treatment.
AB - The resinous wood of Aquilaria sinensis, known as agarwood (Chen Xiang in Chinese), is traditionally used for the treatment of abdominal pain, vomiting, circulatory disorders, and dyspnea. Four new 2-(2-phenylethyl)-4H-chromen-4-one derivatives, namely 7-methoxy-2-[2-(40-hydroxyphenyl) ethyl]chromone (1), 7-hydroxy-2-[2-(40-methoxyphenyl)ethyl]chromone (2), 5,6-dihydroxy-2-[2-(30-hydroxy-40-methoxyphenyl)ethyl]chromone (3), and 6-hydroxy-5-methoxy-2-(2-phenylethyl) chromone (4), have been isolated from the resinous wood of A. sinensis, together with nine known compounds. The structures of these compounds were determined through spectroscopic and MS analyses. Among the isolated compounds, neopetasan, 7-methoxy-2-(2-phenylethyl)-chromone, 6,7-dimethoxy-2-(2-phenylethyl)chromone, and 6,7-dimethoxy-2-[2-(40-methoxyphenyl) ethyl]chromone inhibited NF-κB activation in LPS-stimulated RAW 264.7 macrophages with relative luciferase activity values of 0.55 ± 0.09, 0.54 ± 0.03, 0.31 ± 0.05, and 0.38 ± 0.14, respectively, versus that of vehicle control (1.03 ± 0.02). In addition, 5,6-dihydroxy-2-[2-(3'-hydroxy-4'-methoxyphenyl)ethyl]chromone, 7-methoxy-2-(2-phenylethyl)chromone, 7-dimethoxy-2-(2-phenylethyl)chromone, and 6,7-dimethoxy-2-[2-(4'-methoxyphenyl)ethyl]chromone could suppress LPS-induced NO production in RAW264.7 cells and did not induce cytotoxicity against RAW264.7 cells after 24-h treatment.
KW - 2-(2-phenylethyl)-4h-chromen-4-one
KW - Anti-inflammatory activity
KW - Aquilaria sinensis
KW - Resinous wood
KW - Structure elucidation
KW - Thymelaeaceae
UR - http://www.scopus.com/inward/record.url?scp=85041608329&partnerID=8YFLogxK
U2 - 10.3390/molecules23020289
DO - 10.3390/molecules23020289
M3 - Article
C2 - 29385754
AN - SCOPUS:85041608329
SN - 1420-3049
VL - 23
JO - Molecules
JF - Molecules
IS - 2
M1 - 289
ER -