Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts

Phytochemical analysis of the methanolic and dichloromethane extracts of the aerial parts of Scutellaria pinnatifida led to the isolation of a phenylpropanoid, 1-o-feruloyl-ß-D-glucose [1], two known flavonoids including luteolin-7-o-glucoside (2) and apigenin-7-o-glucoside (3), three known phenylet...

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Main Authors: Abbas Delazar (Author), Hossein Nazemiyeh (Author), Fariba Heshmati Afshar (Author), Niloofar Barghi (Author), Solmaz Esnaashari (Author), Parina Asgharian (Author)
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Published: Wolters Kluwer Medknow Publications, 2017-01-01T00:00:00Z.
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100 1 0 |a Abbas Delazar  |e author 
700 1 0 |a Hossein Nazemiyeh  |e author 
700 1 0 |a Fariba Heshmati Afshar  |e author 
700 1 0 |a Niloofar Barghi  |e author 
700 1 0 |a Solmaz Esnaashari  |e author 
700 1 0 |a Parina Asgharian  |e author 
245 0 0 |a Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts 
260 |b Wolters Kluwer Medknow Publications,   |c 2017-01-01T00:00:00Z. 
500 |a 1735-5362 
500 |a 1735-9414 
500 |a 10.4103/1735-5362.207199 
520 |a Phytochemical analysis of the methanolic and dichloromethane extracts of the aerial parts of Scutellaria pinnatifida led to the isolation of a phenylpropanoid, 1-o-feruloyl-ß-D-glucose [1], two known flavonoids including luteolin-7-o-glucoside (2) and apigenin-7-o-glucoside (3), three known phenylethanoid glycosides composed of phlomisethanoside (4), syringalide A (5), and verbascoside (6), and oleic acid (7). Isolation and structural elucidation of compounds were accomplished by HPLC and spectroscopic methods (UV, 1H- NMR, 13C-NMR). The extracts were also evaluated for their radical scavenging activity and insecticidal property by 2,2-diphenyl-1-picryl-hydrazyl (DPPH) assay and contact toxicity method, respectively. Among the extracts, the methanol extract showed the most potent free radical scavenging activity with a RC50 value of 0.044 ± 0.350 mg/mL which could be attributed to the presence of the isolated phenolic compounds. In the case of insecticidal activity, the n-hexane extract displayed the most potent activity and caused 10%, 15%, and 40% mortality to Oryzaephilus mercator at the concentration of 5, 10, and 15 mg/mL after 4 h of exposure. 
546 |a EN 
690 |a scutellaria pinnatifida; phenylpropanoid; antioxidant activity; insecticidal activity 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Research in Pharmaceutical Sciences, Vol 12, Iss 3, Pp 187-195 (2017) 
787 0 |n http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2017;volume=12;issue=3;spage=187;epage=195;aulast=Delazar 
787 0 |n https://doaj.org/toc/1735-5362 
787 0 |n https://doaj.org/toc/1735-9414 
856 4 1 |u https://doaj.org/article/a2c8399a5ee54a3c91e5df11e3d5a689  |z Connect to this object online.