2000
DOI: 10.1002/1521-4184(20008)333:8<275::aid-ardp275>3.0.co;2-4
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A New Flavonoid fromLimonium axillare

Abstract: A new flavonol glycoside identified as myricetin 3‐O‐β‐D‐sor‐boside (1) has been isolated from the leaves of L. axillare. The new compound showed a moderate inhibition of Ehrlich ascites carci‐noma cells.

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Cited by 19 publications
(2 citation statements)
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“…( Morgan and Funnell, 2018 ; González-Orenga et al., 2021 ). Other species have ethnopharmacological uses against several ailments, including cardiovascular and inflammatory conditions, ( Aniya et al., 2002 ; Murray et al., 2004 ; González-Orenga et al., 2021 ), are rich in bioactive polyphenolic compounds, in particular flavonoids ( Lin and Chou, 2000 ; Ye and Huang, 2006 ; Geng et al., 2015 ), and display several functional properties, such as antioxidant, anti-inflammatory and immunomodulation ( Kandil et al., 2000 ; Aniya et al., 2002 ; Kuo et al., 2002 ; Mahasneh, 2002 ; Murray et al., 2004 ; Cantrell et al., 2007 ; Smirnova et al., 2009 ; Lee et al., 2011 ; Nostro et al., 2012 ; Tang et al., 2012 ; Saidana et al., 2013 ; Ali et al., 2013 ; Rodrigues et al., 2015 ; Souid et al., 2019 ).…”
Section: Introductionmentioning
confidence: 99%
“…( Morgan and Funnell, 2018 ; González-Orenga et al., 2021 ). Other species have ethnopharmacological uses against several ailments, including cardiovascular and inflammatory conditions, ( Aniya et al., 2002 ; Murray et al., 2004 ; González-Orenga et al., 2021 ), are rich in bioactive polyphenolic compounds, in particular flavonoids ( Lin and Chou, 2000 ; Ye and Huang, 2006 ; Geng et al., 2015 ), and display several functional properties, such as antioxidant, anti-inflammatory and immunomodulation ( Kandil et al., 2000 ; Aniya et al., 2002 ; Kuo et al., 2002 ; Mahasneh, 2002 ; Murray et al., 2004 ; Cantrell et al., 2007 ; Smirnova et al., 2009 ; Lee et al., 2011 ; Nostro et al., 2012 ; Tang et al., 2012 ; Saidana et al., 2013 ; Ali et al., 2013 ; Rodrigues et al., 2015 ; Souid et al., 2019 ).…”
Section: Introductionmentioning
confidence: 99%
“…C) of compounds 1 and 2, and the chemical shifts (Dd C ) for sugar carbons by comparison with 3.N.-N. Kong et al 372 determined as quercetin-3-O-(3 00 -Otigloyl)-a-L-rhamnopyranoside. In addition to the above-mentioned new flavonoids, 10 known compounds including quercetin-3-O-a-L-rhamnopyranoside (3) [13], myricetin-3-O-(2 00 -O-galloyl)-a-Lrhamnopyranoside (4) [5,14,15], myricetin-3-O-(3 00 -O-galloyl)-a-L-rhamnopyranoside (5) [5,15], myricetin-3-O-a-L-rhamnopyranoside (6) [16], kaempferol-3-O-a-L-rhamnopyranoside (7)[17], apigenin (8)[13], luteolin(9)…”
mentioning
confidence: 99%