Journal
JOURNAL OF NATURAL PRODUCTS
Volume 72, Issue 4, Pages 613-620Publisher
AMER CHEMICAL SOC
DOI: 10.1021/np800378q
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Four new flavonoid glucosides, 3',4'-di-O-methylquercetin-7-O-[(4 ''-> 13''')-2''',6''',10''',14'''-tetramethylhexadec-13'''-ol- 14'''-enyl]-beta-D-glucopyranoside (1), 4'-O-methylkaempferol-3-O-[(4 ''-> 13''')- 2''',6''', 10''', 14'''-tetramethyl hex adecan-13'''-olyl]-beta-D-glucopyranoside (2), 3',4'-di-O-methylbutin-7-O-[(6 ''-> 1''')-3''', 11'''-dimethyl-7'''-methylenedodeca-3''', 10'''-dienyl]-beta-D-glucopyranoside (3), and 4'-O-methylbutin-7-O-[(6 ''-> 1''')-3''', 11'''-dimethyl-7'''-hydroxymethylenedodecanyl]-beta-D-glucopyranoside (4), along with the three known compounds were isolated from the methanol extract of Catharanthus roseus hairy roots. Their structures were elucidated spectroscopically. The new flavonoid glucosides inhibited both MMP-9 activity and TNF-alpha production in THP-1 cells treated with lipopolysaccharide.
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