A new cyclic diarylheptanoid, 1,5-epoxy-3-hydroxy-1-（3-methoxy-4,5-dihydroxyphenyl）-7-（4-hydroxyphenyl）-heptane （1）, as well as a new monoterpene, 10-O-β-n-glucopyranosyl-hydroxy cineole （2） were isolated fro...A new cyclic diarylheptanoid, 1,5-epoxy-3-hydroxy-1-（3-methoxy-4,5-dihydroxyphenyl）-7-（4-hydroxyphenyl）-heptane （1）, as well as a new monoterpene, 10-O-β-n-glucopyranosyl-hydroxy cineole （2） were isolated from the rhizomes of Zingiber officinale. The structures of compounds 1 and 2 were established based on their spectral data. In addition, the antioxidant activities of these compounds were also measured.展开更多
Twelve 23-esterified silybin derivatives with different patterns of substituents such as aromatic and aliphatic groups （1-12） were designed and synthesized. The antioxidative properties of these compounds were evalu...Twelve 23-esterified silybin derivatives with different patterns of substituents such as aromatic and aliphatic groups （1-12） were designed and synthesized. The antioxidative properties of these compounds were evaluated. The modifed silybin analogues exhibited improved inhibitory effects against rat liver homogenate lipid peroxidation compared to silybin, with exception of the trimethoxylated ester （5） and the aliphatic one （9）. Compounds 3, 5, 7, 8 and 11 displayed their protective properties on DNA cleavage in a dose-dependent manner. 2009 Xiao Kun Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
Three new diarylheptanoids, i.e., sodium（5S,2E）- 1,7-bis（4-hydroxyphenyl）- 1-hydroxy-2-hepten-5 -sulfonate （1）, sodium（5R,2E）-1,7-bis（4-hydroxyphenyl）-1-hydroxy-2-hepten-5-sulfonate （2） and 3,5-diacetoxy-1...Three new diarylheptanoids, i.e., sodium（5S,2E）- 1,7-bis（4-hydroxyphenyl）- 1-hydroxy-2-hepten-5 -sulfonate （1）, sodium（5R,2E）-1,7-bis（4-hydroxyphenyl）-1-hydroxy-2-hepten-5-sulfonate （2） and 3,5-diacetoxy-1-（3-methoxy-4,5-dihydroxyphenyl）-7-（4-hydroxy-3-methoxyphenyl）heptane （3） were isolated from the rhizomes of Zingiber officinale. The structures of the new compounds were elucidated on the basis of spectroscopic methods. The antioxidant activities of 3 were assayed by in vitro models involving DPPH free radicals and superoxide anion radicals.展开更多
Three new compounds, including one chloro-furoeremophilanoid （1）, one eremophiladiolide （2）, a rare dimer of nor- furoeremophilanoid, ligulatrovine A （3）, and a known furoeremophilanolide （4）, were isolated fr...Three new compounds, including one chloro-furoeremophilanoid （1）, one eremophiladiolide （2）, a rare dimer of nor- furoeremophilanoid, ligulatrovine A （3）, and a known furoeremophilanolide （4）, were isolated from Ligularia atroviolacea. The structures of compounds 1-4 were elucidated by spectroscopic methods including 1D and 2D NMR experiments as well as X- ray diffraction study.展开更多
A new sesquiterpene lactone glucoside, notoserolide C (1), was isolated from the whole plant of Notoseris psilolepis Shih. By means of spectral analysis including MS, NMR (H-1 NMR, C-13 NMR, H-1-H-1 COSY, HMQC, HMBC) ...A new sesquiterpene lactone glucoside, notoserolide C (1), was isolated from the whole plant of Notoseris psilolepis Shih. By means of spectral analysis including MS, NMR (H-1 NMR, C-13 NMR, H-1-H-1 COSY, HMQC, HMBC) and X-ray diffraction, the structure of notoserolide C was established as cichorioside B angelate.展开更多
文摘A new cyclic diarylheptanoid, 1,5-epoxy-3-hydroxy-1-（3-methoxy-4,5-dihydroxyphenyl）-7-（4-hydroxyphenyl）-heptane （1）, as well as a new monoterpene, 10-O-β-n-glucopyranosyl-hydroxy cineole （2） were isolated from the rhizomes of Zingiber officinale. The structures of compounds 1 and 2 were established based on their spectral data. In addition, the antioxidant activities of these compounds were also measured.
基金supported by 985 foundation from Zhejiang University and intramural foundation from Wenzhou Medical College
文摘Twelve 23-esterified silybin derivatives with different patterns of substituents such as aromatic and aliphatic groups （1-12） were designed and synthesized. The antioxidative properties of these compounds were evaluated. The modifed silybin analogues exhibited improved inhibitory effects against rat liver homogenate lipid peroxidation compared to silybin, with exception of the trimethoxylated ester （5） and the aliphatic one （9）. Compounds 3, 5, 7, 8 and 11 displayed their protective properties on DNA cleavage in a dose-dependent manner. 2009 Xiao Kun Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
文摘Three new diarylheptanoids, i.e., sodium（5S,2E）- 1,7-bis（4-hydroxyphenyl）- 1-hydroxy-2-hepten-5 -sulfonate （1）, sodium（5R,2E）-1,7-bis（4-hydroxyphenyl）-1-hydroxy-2-hepten-5-sulfonate （2） and 3,5-diacetoxy-1-（3-methoxy-4,5-dihydroxyphenyl）-7-（4-hydroxy-3-methoxyphenyl）heptane （3） were isolated from the rhizomes of Zingiber officinale. The structures of the new compounds were elucidated on the basis of spectroscopic methods. The antioxidant activities of 3 were assayed by in vitro models involving DPPH free radicals and superoxide anion radicals.
基金part financially supported by DAAD-CSC PPP project (No.CSC [2004] 3067) and intramural foundation from Wenzhou Medical College.
文摘Three new compounds, including one chloro-furoeremophilanoid （1）, one eremophiladiolide （2）, a rare dimer of nor- furoeremophilanoid, ligulatrovine A （3）, and a known furoeremophilanolide （4）, were isolated from Ligularia atroviolacea. The structures of compounds 1-4 were elucidated by spectroscopic methods including 1D and 2D NMR experiments as well as X- ray diffraction study.
基金the Special Project of Biological Science and Technology of the Chinese Academy of Sciences (STZ-97-3-08).
文摘A new sesquiterpene lactone glucoside, notoserolide C (1), was isolated from the whole plant of Notoseris psilolepis Shih. By means of spectral analysis including MS, NMR (H-1 NMR, C-13 NMR, H-1-H-1 COSY, HMQC, HMBC) and X-ray diffraction, the structure of notoserolide C was established as cichorioside B angelate.
