2012
DOI: 10.1248/cpb.c12-00174
|View full text |Cite
|
Sign up to set email alerts
|

Antioxidant and Anti-nitric Oxide Components from <i>Quercus glauca</i>

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
4
0

Year Published

2012
2012
2021
2021

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 14 publications
(5 citation statements)
references
References 27 publications
(26 reference statements)
1
4
0
Order By: Relevance
“…Compounds 5 , 10 , and 12 showed moderate DPPH radical scavenging activities with IC 50 values of 42.6 ± 1.8, 57.0 ± 2.3, and 59.5 ± 3.5 μM, respectively, whereas the other compounds (IC 50 > 100 μM) did not display significant DPPH radical scavenging activity (Table ). These results are comparable to those of previously isolated neolignan in other studies. , Zhao et al reported that two new neolignan glycosides (IC 50 > 100 μM) from Pittosporum glabratum were inactive in the DPPH radical scavenging assay . A comparison of the structures of 5 , 10 , and 12 with those of 15 , 8 , and 11 indicated that additional methoxy groups at C-5 positions appeared to increase the antioxidant activity of the dihydrobenzofuran neolignans.…”
Section: Resultssupporting
confidence: 86%
See 1 more Smart Citation
“…Compounds 5 , 10 , and 12 showed moderate DPPH radical scavenging activities with IC 50 values of 42.6 ± 1.8, 57.0 ± 2.3, and 59.5 ± 3.5 μM, respectively, whereas the other compounds (IC 50 > 100 μM) did not display significant DPPH radical scavenging activity (Table ). These results are comparable to those of previously isolated neolignan in other studies. , Zhao et al reported that two new neolignan glycosides (IC 50 > 100 μM) from Pittosporum glabratum were inactive in the DPPH radical scavenging assay . A comparison of the structures of 5 , 10 , and 12 with those of 15 , 8 , and 11 indicated that additional methoxy groups at C-5 positions appeared to increase the antioxidant activity of the dihydrobenzofuran neolignans.…”
Section: Resultssupporting
confidence: 86%
“…These results are comparable to those of previously isolated neolignan in other studies. 44,45 Zhao et al reported that two new neolignan glycosides (IC 50 > 100 μM) from Pittosporum glabratum were inactive in the DPPH radical scavenging assay. 46 A comparison of the structures of 5, 10, and 12 with those of 15, 8, and 11 indicated that additional methoxy groups at C-5 positions appeared to increase the antioxidant activity of the dihydrobenzofuran neolignans.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%
“…), Fagaceae, or the “ring-cup oak”, is native to subtropical and warmer temperate zones of Asia. It contains a variety of tannins (catechins, procyanidins, gallic acids), triterpenoids, flavonoid glycosides and steroids (cycloartanols, stigmastanes) (Kamano et al, 1976, Shen et al, 2012, Sheu et al, 1992, Suga and Kondo, 1974, Wakamatsu et al, 2020)). Schima superba Gardner & Champ., Theaceae, is a dominant broad-leaved evergreen tree distributed over temperate Asia.…”
Section: Methodsmentioning
confidence: 99%
“…The known isolated compounds were identified as 1,3,6-tri- O -galloyl-β- d -glucopyranoside, 3 , 1,2,6-tri- O -galloyl-β- d -glucopyranoside, 4 , 1,2,3-tri- O -galloyl-β- d -glucopyranoside, 5 , 1,2,3,6-tetra- O -galloyl-β- d -glucopyranoside, 6 , 1,2,3,4,6-penta- O -galloyl-β- d -glucopyranoside, 7 , tellimagrandin II, 8 , (7 R ,8 S )-dihydrodehydrodiconiferyl alcohol, 9 , (7 S ,8 R )-dihydrodehydrodiconiferyl alcohol-9-β- d -glucopyranoside, 10 , (7 S ,8 R )-dihydrodehydrodiconiferyl alcohol-9′-β- d -glucopyranoside, 11 , (7 S ,8 R )-urolignoside, 12 , (+)-isolariciresinol, 13 , naringenin, 15 , naringenin 7- O -β- d -glucopyranoside, 16 , 4-hydroxybenzoic acid, 18 , gallic acid, 19 , methyl gallate, 20 , ethyl gallate, 21 , trans - p -hydroxycinnamic acid, 22 , caffeic acid, 23 , and 4-allyl-2-methoxyphenyl-β- d -glucopyranoside, 24 . These compounds were elucidated by comparing their NMR analysis and physical data with literature data.…”
Section: Resultsmentioning
confidence: 99%