Bodiniosides S-Y, Seven New Triterpenoid Saponins from Elsholtzia bodinieri and Their Anti-Influenza Activities.

Investigation of the n-BuOH extract of the aerial parts of Elsholtzia bodinieri led to the isolation of seven new triterpenoid saponins, Bodiniosides S-Y (1-7, resp.). Their strictures were elucidated on the basis of spectroscopic techniques, including HSQC, HSBC, and HSQC-TOCSY experiments, together with acid hydrolysis and GC analysis. The anti-influenza activities of compounds 1-7 were evaluated against A/WSN/33/2009 (H1N1) virus in MDCK cells. The results showed that compounds 2 and 5 exhibited moderate anti-influenza activities against A/WSN/33/2009 (H1N1), with inhibition rates of 35.33% and 24.08%, respectively.

Antiviral and anti-inflammatory activities of chemical constituents from twigs of Mosla chinensis Maxim.

Seven undescribed compounds, including three flavones (1-3), one phenylpropanoid (19), three monoaromatic hydrocarbons (27-29), were isolated from the twigs of Mosla chinensis Maxim together with twenty-eight known compounds. The structures were characterized by HRESIMS, 1D and 2D NMR, and ECD spectroscopic techniques. Compound 20 displayed the most significant activity against A/WSN/33/2009 (H1N1) virus (IC50 = 20.47 µM) compared to the positive control oseltamivir (IC50 = 6.85 µM). Further research on the anti-influenza mechanism showed that compound 20 could bind to H1N1 virus surface antigen HA1 and inhibit the early attachment stage of the virus. Furthermore, compounds 9, 22, 23, and 25 displayed moderate inhibitory effects on the NO expression in LPS inducing Raw 264.7 cells with IC50 values of 22.78, 20.47, 27.66, and 30.14 µM, respectively.

Two new oleanane triterpenoid saponins from Elsholtzia bodinieri.

Two new oleanane triterpenoid saponins, bodiniosides Q (1) and R (2), along with five known saponins, niga-ichigoside F1 (3), 3-O-[ß-D-glucopyranosyl]-28-O-[α-L-rhamnopyranosyl -(1→2)-ß-D-glucopyranosyl] arjunolic acid (4), asiaticoside E (5), sericoside (6), and bodinioside E (7), were isolated from the aerial parts of Elsholtzia bodinieri. The structures of 1 and 2 were characterized by spectroscopic techniques and chemical evidence as 3-O-ß-D- xylopyranosyl-2α, 23-dihydroxy-olean-12-en-28-oic acid 28-O-α-L-rhamnopyranosyl- (1→2)-ß-D-glucopyranoside (1) and 3-O-ß-D-xylopyranosyl-2α, 23-dihydroxy-olean-12-en-28-oic acid 28-O-[ß-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl -(1→2)]-ß-D-glucopyranoside (2). Compounds 1, 3, and 5 exhibited weak anti-influenza activity against strain A/WSN/33/2009 (H1N1), with inhibition rate of 11.63%, 17.01%, and 16.98%, respectively.