Antioxidant, antimutagenic and antitumor activities of flavonoids from the seed shells of Juglans mandshurica

Author(s):  
H Xu ◽  
G Xia ◽  
Y Bao
Separations ◽  
2021 ◽  
Vol 8 (9) ◽  
pp. 132
Author(s):  
Hong Yang ◽  
Li-Bo Wang ◽  
Ya-Ping Guo ◽  
Ya-Li Wang ◽  
Xiao-Xiang Chen ◽  
...  

The immature epicarps of Juglans mandshurica and Juglans regia have been used as folk medicine for the treatment of cancer in China. Other parts of the J.mandshurica plant, including leaves, branches, barks, and stems, have reported antitumor activities. We previously found that various diarylheptanoids and phenolic compounds isolated from J. mandshurica epicarps show significant antitumor activities. However, there are no reports of quantitative analysis of diarylheptanoids and phenolic compounds of J. mandshurica. In this study, a validated quantitative method, based on ultraperformance liquid chromatography coupled with triple-quadrupole tandem mass spectrometry, was employed to determine the contents of eight diarylheptanoids and seven phenolic compounds in the epicarps of J. mandshurica during different growth periods, in different parts of the plant, and in the epicarps of two Juglans species. The most successful J. mandshurica epicarp harvesting time fell between Day 12 and Day 27. The leaves of J. mandshurica showed potential for medical use as they had the highest content of the 15 compounds (3.399 ± 0.013 mg/g). We showed for the first time that the total content of diarylheptanoids in J. mandshurica is higher than that in J. regia, though, conversely, J. regia has higher contents of phenolic compounds. The method developed in this study is practical and simple and can be applied for quantitative analysis for evaluating the intrinsic quality of J. mandshurica.


Planta Medica ◽  
2010 ◽  
Vol 76 (12) ◽  
Author(s):  
F Pehlivan Karakas ◽  
A Ucar Turker ◽  
F Yalçin ◽  
I Çalis
Keyword(s):  

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381 ◽  
Author(s):  
SJ Park ◽  
N Kim ◽  
G Yoo ◽  
JH Park ◽  
SH Kim
Keyword(s):  

2011 ◽  
Vol 3 (7) ◽  
pp. 106-110
Author(s):  
Mohamed Abd El-Moneim ◽  
◽  
Ibrahim M El-Deen ◽  
Wessam Abd El-Fattah

2016 ◽  
Vol 12 (8) ◽  
pp. 311-317
Author(s):  
Kamelia El-Mahdy

Thiazolopyrimidine 2 was obtained from the reaction of dihydropyrimidinone with chloroacetic acid and benzaldehyde. Thiazolopyrimidine 2 containing an α,β-unsaturated ketonic function [-CH=CH-CO-] has been used as a component of Michael addition with an equimolar amount of dinucleophiles to give a series of novel tetracyclic pyrimidine derivatives. Treatment of thiazolopyrimidine 2 with uracil, aminotriazole, cyanoacetic acid hydrazide, o-phenylenediamine or diaminopyridine afforded the corresponding pyridopyrimidine, triazolopyrimidine, pyrazolone, benzodiazepine and triazepine derivative, respectively. The detailed synthesis, spectroscopic data, and antitumor activity for synthesized compounds were reported.


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