期刊
JOURNAL OF NATURAL PRODUCTS
卷 72, 期 4, 页码 613-620出版社
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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