A newα-tetralonyl glucoside,6'-O-acetyl-juglanoside E(1),and a new dihydrophaseic acid glucoside,dihydrophaseic acid 1-O-(6-O-acetyl)-glucopyranoside(2),together with two known ones,juglanoside E(3)and dihydropha...A newα-tetralonyl glucoside,6'-O-acetyl-juglanoside E(1),and a new dihydrophaseic acid glucoside,dihydrophaseic acid 1-O-(6-O-acetyl)-glucopyranoside(2),together with two known ones,juglanoside E(3)and dihydrophaseic acid(4),were isolated from the pellicle of the walnut(Juglans regia).The structures of the new compounds were elucidated by comprehensive spectroscopic analysis,including IR,HRESIMS,1D and 2D NMR data.展开更多
Nineteen alkaloids,including a new C19-diterpenoid alkaloid stapfianine A(1)and a new benzamide derivative stapfianine B(2)were isolated from the roots of Aconitum stapfianum.Their structures were established on the b...Nineteen alkaloids,including a new C19-diterpenoid alkaloid stapfianine A(1)and a new benzamide derivative stapfianine B(2)were isolated from the roots of Aconitum stapfianum.Their structures were established on the basis of extensive spectroscopic analyses(IR,HRESIMS,1D and 2D NMR).展开更多
The tribe Delphineae,comprising two genera,Aconitum L.and Delphinium L.,is the richest source of bioactive diterpenoid alkaloids(DAs),while their highly similar chemical structures create a major challenge for derepli...The tribe Delphineae,comprising two genera,Aconitum L.and Delphinium L.,is the richest source of bioactive diterpenoid alkaloids(DAs),while their highly similar chemical structures create a major challenge for dereplication from complex mixture.To solve the inefficient discovery process of natural DAs,a novel dereplication strategy based on pattern recognition of specific heteronuclear multiple bond correlation(HMBC)signals has been established in this study.This strategy utilized the diagnostic signals in the HMBC spectra of C_(19)-DAs,which could indicate the structural categories.The newly designed software MatchNat allowed in silico recognition of C_(19)-DA types.The developed dereplication system was demonstrated to be a practical strategy to dereplicate a variety of natural products from two Delphineae plants,including Aconitum vilmorinianum Kom.and Delphinium pachycentrum Hemsl.Known compounds could be rapidly recognized from the mixture,and novel DAs were found with the aid of MatchNat.Consequently,targeted isolation led to the explosive discovery of a series of novel DAs.This dereplication system has the potential to be adopted for dereplication of any other class of natural products and has shown promising application as a complementary tool in the nuclear magnetic resonance analysis of traditional Chinese medicines.展开更多
基金supported by a program for New Century Excellent Talents in University from MOE(No.NCET-08-0925)together with a grant from the Natural Science Foundation of China(21002084)+2 种基金grants from the Natural Science Foundation of the Yunnan Province(Nos.2008CD066,2010CD017)an Undergraduates Innovative Experiment Project from MOE(101067320)as well as grants from Key Laboratory of Medicinal Chemistry for Nature Resource,MOE(Nos.2009102204,2009102202).
文摘A newα-tetralonyl glucoside,6'-O-acetyl-juglanoside E(1),and a new dihydrophaseic acid glucoside,dihydrophaseic acid 1-O-(6-O-acetyl)-glucopyranoside(2),together with two known ones,juglanoside E(3)and dihydrophaseic acid(4),were isolated from the pellicle of the walnut(Juglans regia).The structures of the new compounds were elucidated by comprehensive spectroscopic analysis,including IR,HRESIMS,1D and 2D NMR data.
基金This project was financially supported by grants from the National Natural Science Foundation of China(No.81460648)the Program for Changjiang Scholars and Innovative Research Team in University(No.IRT13095)from the Postgraduate Foundation of Yunnan University(No.YNUY201415).
文摘Nineteen alkaloids,including a new C19-diterpenoid alkaloid stapfianine A(1)and a new benzamide derivative stapfianine B(2)were isolated from the roots of Aconitum stapfianum.Their structures were established on the basis of extensive spectroscopic analyses(IR,HRESIMS,1D and 2D NMR).
基金Project supported by the National Natural Science Foundation of China(No.81460648)the Program for Changjiang Scholars and Innovative Research Team in University(No.IRT13095),China
基金funded by the Science and Technology Development Fund,Macao SAR(File Nos.0023/2019/AKP,0077/2019/A2,0002/2019/APD,and 0040/2021/AGJ)the National Natural Science Foundation of China(No.31860095)。
文摘The tribe Delphineae,comprising two genera,Aconitum L.and Delphinium L.,is the richest source of bioactive diterpenoid alkaloids(DAs),while their highly similar chemical structures create a major challenge for dereplication from complex mixture.To solve the inefficient discovery process of natural DAs,a novel dereplication strategy based on pattern recognition of specific heteronuclear multiple bond correlation(HMBC)signals has been established in this study.This strategy utilized the diagnostic signals in the HMBC spectra of C_(19)-DAs,which could indicate the structural categories.The newly designed software MatchNat allowed in silico recognition of C_(19)-DA types.The developed dereplication system was demonstrated to be a practical strategy to dereplicate a variety of natural products from two Delphineae plants,including Aconitum vilmorinianum Kom.and Delphinium pachycentrum Hemsl.Known compounds could be rapidly recognized from the mixture,and novel DAs were found with the aid of MatchNat.Consequently,targeted isolation led to the explosive discovery of a series of novel DAs.This dereplication system has the potential to be adopted for dereplication of any other class of natural products and has shown promising application as a complementary tool in the nuclear magnetic resonance analysis of traditional Chinese medicines.
