2015
DOI: 10.1016/j.bmcl.2014.12.055
|View full text |Cite
|
Sign up to set email alerts
|

Anti-inflammatory activity of phenolic compounds from the whole plant of Scutellaria indica

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
21
0

Year Published

2017
2017
2020
2020

Publication Types

Select...
8

Relationship

2
6

Authors

Journals

citations
Cited by 28 publications
(25 citation statements)
references
References 22 publications
2
21
0
Order By: Relevance
“…Phenolics including alkenyl phenols are essential compounds for the suppression of inflammation among phytochemicals. Cuong et al studied the anti-inflammatory effects of phenolic compounds, and the results showed a strong inhibitory on NO production of isolated compounds because of the presence of the conjugated double bond of the olefinic group, and the 3,4-hydroxylation(s) of benzene ring gave favorable results [31,32,40]. In our study, bavinol A (4), which belongs to the alkenyl phenol class, exhibited the strongest inhibitory on NO production among the isolated compounds.…”
Section: No Production Inhibition and The Cell Viability Assaysupporting
confidence: 51%
See 1 more Smart Citation
“…Phenolics including alkenyl phenols are essential compounds for the suppression of inflammation among phytochemicals. Cuong et al studied the anti-inflammatory effects of phenolic compounds, and the results showed a strong inhibitory on NO production of isolated compounds because of the presence of the conjugated double bond of the olefinic group, and the 3,4-hydroxylation(s) of benzene ring gave favorable results [31,32,40]. In our study, bavinol A (4), which belongs to the alkenyl phenol class, exhibited the strongest inhibitory on NO production among the isolated compounds.…”
Section: No Production Inhibition and The Cell Viability Assaysupporting
confidence: 51%
“…In our study, bavinol A (4), which belongs to the alkenyl phenol class, exhibited the strongest inhibitory on NO production among the isolated compounds. However, the inhibitory activities on NO production of bavinol A (4) were weaker than active compounds presumably because of the lack of 3-hydroxylation of the benzene ring [31,32,40]. Compound 5 (transphytol) containing the conjugated double bond of the olefinic group in the structure also exhibited a strong inhibitory on NO production.…”
Section: No Production Inhibition and The Cell Viability Assaymentioning
confidence: 99%
“…The 13 C‐NMR ((D 6 )DMSO, 125 MHz) and DEPT spectra gave 25 carbon resonances, including one methyl, three methylenes (sp 3 hybridized), thirteen methines (eight sp 2 hybridized and five sp 3 hybridized), and eight quaternary carbons (sp 2 hybridized). Detailed analyses of above 25 carbon signals displayed that 15 carbons were due to one flavonoid skeleton, six carbons to one glucuronate moiety, and four carbons to one butyl group, respectively. In the HMBC experiment ( Figure ), the long‐range correlations from δ (H) 12.83 (1H, s, 5‐OH) to δ (C) 161.6 (C(5)), δ (H) 5.33 (1H, d, J = 7.3, H–C(1″)) to δ (C) 163.1 (C(7)) and δ (H) 4.04 – 4.15 (2H, m, H–C(1‴)) to δ (C) 169.2 (C(6″)) confirmed the hydroxy group, glucuronate ester moiety, and butyl group were attached to C(5), C(7), and C(6″), respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Phenolic compounds, broadly distributed in the plant kingdom, are a major class of bioactive components. Phenols and flavonoids have drawn increasing attention due to their marked effects in the prevention of various diseases as these possess diverse biological activities, for instance, antioxidant [43], antitumor [44], antiulcer [45], anti-inflammatory [43,46] and antidepressant activities [47,48].…”
Section: Phenol and Flavonoid Estimationmentioning
confidence: 99%