TY - JOUR
T1 - Anti-inflammatory and neuroprotective constituents from the peels of citrus grandis
AU - Kuo, Ping Chung
AU - Liao, Yu Ren
AU - Hung, Hsin Yi
AU - Chuang, Chia Wei
AU - Hwang, Tsong Long
AU - Huang, Shiow Chyn
AU - Shiao, Young Ji
AU - Kuo, Daih Huang
AU - Wu, Tian Shung
N1 - Publisher Copyright:
© 2017 by the authors.
PY - 2017/6
Y1 - 2017/6
N2 - A series of chromatographic separations performed on the ethanol extracts of the peels of Citrus grandis has led to the characterization of forty compounds, including seventeen coumarins, eight flavonoids, two triterpenoids, four benzenoids, two steroids, one lignan, one amide, and five other compounds, respectively. The chemical structures of the purified constituents were identified on the basis of spectroscopic elucidation, including 1D- and 2D-NMR, UV, IR, and mass spectrometric analysis. Most of the isolated compounds were examined for their inhibition of superoxide anion generation and elastase release by human neutrophils. Among the isolates, isomeranzin (3), 17,18-dihydroxybergamottin (12), epoxybergamottin (13), rhoifolin (19), vitexicarpin (22) and 4-hydroxybenzaldehyde (29) displayed the most significant inhibition of superoxide anion generation and elastase release with IC50 values ranged from 0.54 to 7.57 µM, and 0.43 to 4.33 µM, respectively. In addition, 7-hydroxy-8-(2-hydroxy-3-methylbut-3-enyl)coumarin (8) and 17,18-dihydroxybergamottin (12) also exhibited the protection of neurons against Aβ-mediated neurotoxicity at 50 µM.
AB - A series of chromatographic separations performed on the ethanol extracts of the peels of Citrus grandis has led to the characterization of forty compounds, including seventeen coumarins, eight flavonoids, two triterpenoids, four benzenoids, two steroids, one lignan, one amide, and five other compounds, respectively. The chemical structures of the purified constituents were identified on the basis of spectroscopic elucidation, including 1D- and 2D-NMR, UV, IR, and mass spectrometric analysis. Most of the isolated compounds were examined for their inhibition of superoxide anion generation and elastase release by human neutrophils. Among the isolates, isomeranzin (3), 17,18-dihydroxybergamottin (12), epoxybergamottin (13), rhoifolin (19), vitexicarpin (22) and 4-hydroxybenzaldehyde (29) displayed the most significant inhibition of superoxide anion generation and elastase release with IC50 values ranged from 0.54 to 7.57 µM, and 0.43 to 4.33 µM, respectively. In addition, 7-hydroxy-8-(2-hydroxy-3-methylbut-3-enyl)coumarin (8) and 17,18-dihydroxybergamottin (12) also exhibited the protection of neurons against Aβ-mediated neurotoxicity at 50 µM.
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U2 - 10.3390/molecules22060967
DO - 10.3390/molecules22060967
M3 - Article
C2 - 28598384
AN - SCOPUS:85021121711
SN - 1420-3049
VL - 22
JO - Molecules
JF - Molecules
IS - 6
M1 - 967
ER -