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Lignans and neolignans from the stems of Vibrunum erosum and their neuroprotective and anti-inflammatory activity
A new lignan, (7′ S ,8 S ,8′ S )-3,5′-dimethoxy-3′,4,9′-trihydroxy-7′,9-epoxy-8,8′-lignan, named vibruresinol ( 1 ), was isolated from the stems of Viburnum erosum by silica gel, ODS, and Sephadex LH-20 column chromatography. In addition, four other known lignans, (7′ R ,8 S ,8′ S )-3,5′-dimethoxy-3...
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Published in: | Archives of pharmacal research 2015, 38(1), , pp.26-34 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A new lignan, (7′
S
,8
S
,8′
S
)-3,5′-dimethoxy-3′,4,9′-trihydroxy-7′,9-epoxy-8,8′-lignan, named vibruresinol (
1
), was isolated from the stems of
Viburnum erosum
by silica gel, ODS, and Sephadex LH-20 column chromatography. In addition, four other known lignans, (7′
R
,8
S
,8′
S
)-3,5′-dimethoxy-3′,4,8′,9′-tetrahydroxy-7′,9-epoxy-8,8′-lignan (
2
), (+)-syringaresinol (
3
), (+)-pinoresinol (
4
), and (+)-pinoresinol-4-
O
-
β
-
d
-glucopyranoside (
5
), and five known neolignans, herpetol (
6
), vibsanol (
7
), (−)-dehydrodiconiferyl alcohol (
8
), icariside E
4
(
9
), and dihydrodehydrodiconiferyl alcohol (
10
), were isolated in the same manner. The chemical structures of the compounds were determined based on spectroscopic data including NMR, MS, and IR. All of the compounds described above were isolated from
V. erosum
for the first time. The isolated compounds
3
,
4
, and
6
were evaluated for neuroprotective activity on glutamate-induced cell death in HT22 cells and had EC
50
values of 6.33 ± 1.22, 6.96 ± 0.65, and 9.15 ± 0.36 μM, respectively. Likewise, the same compounds had inhibitory activity on NO production in LPS-induced RAW 264.7 cells with IC
50
values of 8.30 ± 1.56, 7.89 ± 1.22, and 9.32 ± 0.36 μM, respectively. |
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ISSN: | 0253-6269 1976-3786 |
DOI: | 10.1007/s12272-014-0358-9 |