Abstract:
An ethanol extract of
Chloranthus henryi (Chloranthaceae) was subjected to various chromatographic procedures including silica gel column chromatography, MCI column chromatography, Sephadex LH-20 column chromatography, and preparative HPLC. Five purified sesquiterpenes analyzed by spectroscopic analyses (MS, IR, NMR) and single crystal X-ray diffraction were elucidated as (1
S,6
S,8
R)-8-ethoxychlomultin C (
1a), (1
R,6
R,8
S)-8-ethoxychlomultin C (
1b), (+)-phaeocaulin D (
2), atractylenolide Ⅰ (
3), and 8-
β-ethoxyasterolid (
4). Compounds
1a and
1b were a new pair of sesquiterpene enantiomers and compounds
2-
4 were isolated from this plant for the first time. Compounds
1a,
1b,
2 and
3 increased cell viability in H
2O
2-treated PC12 cells from (43.41±1.59)% to (61.71±7.56)%, (66.05±5.61)%, (74.34±3.32)% and (69.58±5.02)% at 10 μmol·L
-1, respectively.