Loading…

Dispolongiosides A and B, Two New Fucose Containing Spirostanol Glycosides From the Rhizomes of Disporopsis longifolia Craib., and Their Nitric Oxide Production Inhibitory Activities

Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1...

Full description

Saved in:
Bibliographic Details
Published in:Natural product communications 2021-10, Vol.16 (10)
Main Authors: Thu Ha, Tran Thi, Vui, Dang Kim, Hoang, Nguyen Huy, Tai, Bui Huu, Van Kiem, Phan
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Two new fucose containing spirostanol glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (1) and (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-fucopyranoside (2), together with five known spirostan glycosides, (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (3), (25S)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (4), (25R)-spirost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (5), (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-methoxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (6), and (25R)-26-[(β-D-glucopyranosyl)oxy]-22α-hydroxyfurost-5-en-3β-yl O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (7) were isolated from the rhizomes of Disporopsis longifolia Craib. Their structures were determined by extensive analysis of HRESIMS and NMR spectral data, as well as by comparison of the spectral data with those reported in the literature. Compounds 1 to 7 inhibited NO production in LPS-activated RAW264.7 cells with IC50 values in the range from 24.5 ± 2.5 μM to 81.3 ± 4.2 μM. The NO production inhibitory activities of compounds 1 and 2 with IC50 values of 26.6 ± 1.9 μM and 24.5 ± 2.5 μM are as potent as that of the positive control of NG-monomethyl-L-arginine acetate (L-NMMA) with an IC50 value of 23.8 ± 2.1 μM.
ISSN:1934-578X
1555-9475
DOI:10.1177/1934578X211055013