Two new β-hydroxy amino acid-coupled secoiridoids, named serinosecologanin （1） and threoninose- cologanin （2）, were isolated from an aqueous extract of the flower buds of Lonicera japonica. Their uncommon structu...Two new β-hydroxy amino acid-coupled secoiridoids, named serinosecologanin （1） and threoninose- cologanin （2）, were isolated from an aqueous extract of the flower buds of Lonicera japonica. Their uncommon structures including absolute configurations were determined by spectroscopic data analysis, and confirmed by semisynthesis from the co-occurring secologanin （3） and secologanic acid （4）. Compounds 1 and 2 exhibited resistant activity against β-glucosidase from almonds and hesperidinase from Aspergillus niger, they also showed activity against the release of glucuronidase in rat polymorphonuclear leukocytes induced by the platelet-activating factor with inhibition rates of （34.9 ±3.1 ）% and （53.6 ± 2.6）%, respectively.展开更多
Two new ar-bisabol sequiterpenes,(+)-(7S,10S)-10-epi-7,10-epoxy-3-hydroxy-ar-bisabol-11-ol(1)and(+)-(7R,8R,10S)-10-epi-7,10-epoxy-8-hydroxy-ar-bisabol-11-ol(2),have been isolated by a combination of various column chr...Two new ar-bisabol sequiterpenes,(+)-(7S,10S)-10-epi-7,10-epoxy-3-hydroxy-ar-bisabol-11-ol(1)and(+)-(7R,8R,10S)-10-epi-7,10-epoxy-8-hydroxy-ar-bisabol-11-ol(2),have been isolated by a combination of various column chromatographic techniques including reversed-phase semipreparative HPLC from an ethanol extract of the stem bark of Fraxinus sielboldiana.Their structures were determined by spectroscopic methods including IR,MS,and 1D and 2D NMR experiments.This is the first report of sequiterpenes in the genus Fraxinus.展开更多
A minor diterpenoid with a novel carbon skeleton,secoeuphoractin（1）,was isolated from an ethanol extract of the roots of Euphorbia micractina.Its structure including the absolute configuration was determined by exte...A minor diterpenoid with a novel carbon skeleton,secoeuphoractin（1）,was isolated from an ethanol extract of the roots of Euphorbia micractina.Its structure including the absolute configuration was determined by extensive spectroscopic studies,especially by 2D NMR and CD data analysis,in combination with a plausible biosynthetic pathway associated with co-occurring diverse diterpenoids.This compound showed activity against HIV-1 replication with an IC_（50） value of 1.76 ± 0.61 μmol/L.展开更多
Two new homosecoiridoids, named loniaceticiridoside （1） and lonimalondialiridoside （2）, were isolated from an aqueous extract of the flower buds of Lonicera japonica. Their structures including the absolute config...Two new homosecoiridoids, named loniaceticiridoside （1） and lonimalondialiridoside （2）, were isolated from an aqueous extract of the flower buds of Lonicera japonica. Their structures including the absolute configuration were determined by extensive spectroscopic studies, especially by 2D NMR and CD data analysis. A proposed biosynthetic pathway and preliminary investigations of the biological activity of compounds 1 and 2 are also discussed.展开更多
基金Financial support from the National Natural Science Foundation of China (NNSFC Nos.20772156 and 30825044)+1 种基金the Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT,No.IRT1007)the National Science and Technology Project of China (Nos.2012ZX09301002-002 and 2011ZX0 9307002-01)
文摘Two new β-hydroxy amino acid-coupled secoiridoids, named serinosecologanin （1） and threoninose- cologanin （2）, were isolated from an aqueous extract of the flower buds of Lonicera japonica. Their uncommon structures including absolute configurations were determined by spectroscopic data analysis, and confirmed by semisynthesis from the co-occurring secologanin （3） and secologanic acid （4）. Compounds 1 and 2 exhibited resistant activity against β-glucosidase from almonds and hesperidinase from Aspergillus niger, they also showed activity against the release of glucuronidase in rat polymorphonuclear leukocytes induced by the platelet-activating factor with inhibition rates of （34.9 ±3.1 ）% and （53.6 ± 2.6）%, respectively.
基金Financial support from the National Natural Sciences Foundation of China(NNSFC,Grant nos.30825044 and 20932007)the National Science and Technology Project of China(Nos.2009ZX09311-004 and 2009ZX09301-003-4-1)is acknowledged.
文摘Two new ar-bisabol sequiterpenes,(+)-(7S,10S)-10-epi-7,10-epoxy-3-hydroxy-ar-bisabol-11-ol(1)and(+)-(7R,8R,10S)-10-epi-7,10-epoxy-8-hydroxy-ar-bisabol-11-ol(2),have been isolated by a combination of various column chromatographic techniques including reversed-phase semipreparative HPLC from an ethanol extract of the stem bark of Fraxinus sielboldiana.Their structures were determined by spectroscopic methods including IR,MS,and 1D and 2D NMR experiments.This is the first report of sequiterpenes in the genus Fraxinus.
基金Financial support from the National Natural Science Foundation of China(NNSFCNos.21172266 and 30825044)+1 种基金the Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT,No.IRT1007)the National Science and Technology Project of China(No.2012ZX09301002-002)
文摘A minor diterpenoid with a novel carbon skeleton,secoeuphoractin（1）,was isolated from an ethanol extract of the roots of Euphorbia micractina.Its structure including the absolute configuration was determined by extensive spectroscopic studies,especially by 2D NMR and CD data analysis,in combination with a plausible biosynthetic pathway associated with co-occurring diverse diterpenoids.This compound showed activity against HIV-1 replication with an IC_（50） value of 1.76 ± 0.61 μmol/L.
基金Financial support from the National Natural Science Foundation of China(NNSFCNos.20772156 and 30825044)+1 种基金the Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT,No.IRT1007)the National Science and Technology Project of China(Nos.2012ZX09301002-002 and 2011ZX0 9307002-01) is acknowledged
文摘Two new homosecoiridoids, named loniaceticiridoside （1） and lonimalondialiridoside （2）, were isolated from an aqueous extract of the flower buds of Lonicera japonica. Their structures including the absolute configuration were determined by extensive spectroscopic studies, especially by 2D NMR and CD data analysis. A proposed biosynthetic pathway and preliminary investigations of the biological activity of compounds 1 and 2 are also discussed.
