Electrospray ionization tandem mass spectrometric analysis of ent-6,7-seco-kaurane diterpenoids from the Isodon species

被引:11
作者
Zhou, Yan [1 ,2 ]
Yang, Bin-Li [3 ]
Yang, Jing [4 ]
Huang, Sheng-Xiong [3 ]
Sun, Han-Dong [3 ]
Xu, Hong-Xi [1 ]
Ding, Li-Sheng [2 ]
机构
[1] Hong Kong Jockey Club Inst Chinese Med, Shatin, Hong Kong, Peoples R China
[2] Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Sichuan Prov, Peoples R China
[3] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming 650204, Yunnan Province, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Chem & Chem Technol, Shanghai 200240, Peoples R China
关键词
ENT-KAURANE DITERPENOIDS; ANTIBACTERIAL ACTIVITY; TERPENOIDS; JAPONICUS; ANTITUMOR;
D O I
10.1002/rcm.3864
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Electrospray ionization tandem mass spectrometry (ESI-MSn) using an ion trap instrument and accurate mass measurement on a quadrupole time-of-flight (Q-TOF) mass spectrometer has aided the structural characterization and differentiation of the enmein and spiro-lactone types of ent-6,7-seco-kaurane diterpenoids from Isodon species. The mass spectral fragmentation data from both techniques was compared to obtain the mass spectrometric fragmentation pathways of the ent-6,7-seco-kaurane diterpenoids with high confidence. The analysis revealed that losses of CH2O and CO2 are the predominant process for the enmein type of ent-kauranes in negative ion mode, and the loss Of CO2 is typical for the spiro-lactone type in positive ion mode. In addition, compounds of the spiro-lactone type with a conserved core structure but different substituent groups, such as acetyl, hydroxyl, and aldehyde moiety, resulted in diagnostic product ions by means of successive losses of AcOH, H2O, and CO, respectively. The fragmentation knowledge will facilitate the analysis and identification of the ent-6,7-seco-kauranes in future plant research. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:138 / 146
页数:9
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