Journal
NATURAL PRODUCT RESEARCH
Volume -, Issue -, Pages -Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/14786419.2023.2174534
Keywords
Achyranthes bidentata; Amaranthaceae; achyranbiden A; achyranbiden B; achyranbiden C; NO production inhibitory activity; antidiabetic activity
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A phytochemical study on the roots of Achyranthes bidentata Blume resulted in the discovery of 16 compounds, including 3 new ones (1-3). Their chemical structures were determined through spectroscopic analysis. Compounds 1, 7, and 11-16 exhibited inhibition of NO production in LPS-activated RAW264.7 cells, with IC50 values ranging from 28.03 to 54.23 μM. Compounds 14 and 15 showed anti-α-glucosidase activity, with IC50 values of 176.24 μM and 156.92 μM, respectively.
Phytochemical study on the roots of Achyranthes bidentata Blume led to the isolation of sixteen compounds including three new ones (1-3). Their chemical structures were determined as oleanolic acid 28-O-beta-D-glucopyranoside-3-O-[beta-D-glucopyranosyl-(1 -> 3)-beta-D-galactopyranoside) (1), methyl (8Z,11Z)-5,6,7-trihydroxytetradeca-8,11-dienoate (2), methyl (6E,11Z)-5,8,9-trihydroxytetradeca-6,11-dienoate (3), fulgidic acid (4), (9E,11E)-13-oxooctadeca-9,11-dienoic acid (5), (9Z,11E,15Z)-13-hydroxyoctadeca-9,11,15-trienoic acid (6), oleanolic acid 28-O-beta-D-glucopyranoside-3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucuronopyranoside (7), oleanolic acid 28-O-beta-D-glucopyranoside-3-O-beta-D-glucopyranosyl-(1 -> 2)-[alpha-L-rhamnopyranosyl-(1 -> 3)]-beta-D-glucuronopyranoside (8), oleanolic acid 3-O-beta-D-glucopyranosyl-(1 -> 2)-[alpha-L-rhamnopyranosyl-(1 -> 3)]-beta-D-glucuronopyranoside (9), oleanolic acid 3-O-alpha-L-rhamnopyranosyl-(1 -> 3)-beta-D-glucuronopyranoside (10), blumenol C glucoside (11), citroside A (12), 6S,9S-roseoside (13), ginsenoside Rg1 (14), 20-hydroxyecdysone (15), and benzyl alpha-L-rhamnopyranosyl-(1 -> 6)]-beta-D-glucopyranoside (16) by spectroscopic analysis. Compounds 1, 7 and 11-16 inhibited NO production in LPS-activated RAW264.7 cells with IC50 values in the range from 28.03 to 54.23 mu M (positive control, L-NMMA: IC50 = 35.52 mu M). Compounds 14 and 15 showed anti alpha-glucosidase activity with IC50 values of 176.24 and 156.92 mu M, respectively, compared with the positive control, acarbose, IC50 = 160.99 mu M.
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