| Literature DB >> 25172104 |
Wenlian Wang1, Jianping Zhao2, Shanshan Li1, Yuchen Lu1, Yanli Liu1, Qiongming Xu3, Xiaoran Li1, Ikhlas A Khan4, Shilin Yang1.
Abstract
Five new ursane-type triterpenoidal saponins (1-5), together with five known ones (6-10), were isolated from the EtOH extract of the roots of Ilex cornuta. The structures of saponins 1-5 were elucidated as 19α-hydroxyurs-12-en-28-oic acid 3β-O-β-D-glucuronopyranoside (1), 19α-hydroxyurs-12-en-28-oic acid 3β-O-β-D-glucuronopyranoside-6-O-ethyl ester (2), 19α-hydroxyurs-12-en-28-oic acid 3β-O-α-L-arabinopyranosyl-(1→2)-β-D-glucuronopyranoside (3), 3β-O-[α-L-arabinopyranosyl-(1→2)-β-D-glucuronopyranosyl]-19α-hydroxyurs-12-en-28-oic acid 28-O-β-D-glucopyranosyl ester (4) and 3β-O-[α-L-arabinopyranosyl-(1→2)-β-D-glucuronopyranoside-6-O-methyl ester]-19α-hydroxyurs-12-en-28-oic acid 28-O-β-D-glucopyranosyl ester (5), on the basis of spectroscopic analyses (IR, ESI-MS, HR-ESI-MS, 1D and 2D NMR) and chemical reactions. Protective effects of compounds 1-10 against H₂O₂-induced H9c2 cardiomyocyte injury were tested. Compounds 1-5, 7, and 10 showed cell-protective effects. Among them compound 5 exhibited the highest activity. No significant DPPH radical scavenging activity was observed for compounds 1-10.Entities:
Keywords: Aquifoliaceae; Cardiomyocytes oxidative injury; DPPH radical scavenging activity; Ilex cornuta; Structure identification; Triterpenoid saponins
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Year: 2014 PMID: 25172104 DOI: 10.1016/j.fitote.2014.08.016
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882