Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Lianqing Shen is active.

Publication


Featured researches published by Lianqing Shen.


Journal of Pharmaceutical and Biomedical Analysis | 2010

Rapid separation and characterization of active flavonolignans of Silybum marianum by ultra-performance liquid chromatography coupled with electrospray tandem mass spectrometry

Kuiwu Wang; Hong Zhang; Lianqing Shen; Qizhen Du; Jianrong Li

Ultra-performance liquid chromatography (UPLC) interfaced with the electrospray ionization (ESI) tandem mass spectrometer (MS(n)) was developed for the simultaneous determination of silychristins A (1) and B (2), silydianin (3), silybins A (4) and B (5), and isosilybins A (6) and B (7), major bioactive flavonolignans in silymarin, a herbal remedy derived from the milk thistle Silybum marianum. In this study, the seven major active flavonolignans including the diastereomers 1/2, 4/5, and 6/7 were completely separated using UPLC with an ACQUITY UPLC C(18) column and a MeOH/water/formic acid mobile phase system. The collision-induced dissociation (CID) MS(n) spectra of these flavonolignans were studied systematically using ESI-MS. The results with the present methodology show that UPLC-MS(n) can be useful for general screening of active natural products from plant extracts and for the specific quality control of silymarin.


Carbohydrate Research | 2011

Novel steroidal saponins from Liriope graminifolia (Linn.) Baker with anti-tumor activities.

Kuiwu Wang; Hong Zhang; Lianqing Shen; Wei Wang

Phytochemical investigation of the underground parts of Liriope graminifolia (Linn.) Baker resulted in the isolation of two new steroidal saponins lirigramosides A (1) and B (2) along with four known compounds. The structures were determined by extensive spectral analysis, including two-dimensional (2D) NMR spectroscopy and chemical methods, to be 3-O-[β-d-xylopyranosyl-(1→3)-α-l-arabinopyranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→4)]-β-d-glucopyranosyl-(25S)-spirost-5-ene-3β,17α-diol (1), 1-O-[α-l-rhamnopyranosyl-(1→2)-β-d-xylopyranosyl]-(25R)-ruscogenin (2), 1-O-β-d-xylopyranosyl-3-O-α-l-rhamnopyranosyl-(25S)-ruscogenin (3), 3-O-α-l-rhamnopyranosyl-1-O-sulfo-(25S)-ruscogenin (4), methylophiopogonanone B (5), and 5,7-dihydroxy-3-(4-methoxybenzyl)-6-methyl-chroman-4-one, (ophiopogonanone B, 6), respectively. Compound 1 has a new (25S)-spirost-5-ene-3β,17α-diol ((25S)-pennogenin) aglycone moiety. The isolated compounds were evaluated for their cytotoxic activities against Hela and SMMC-7721 cells.


Asian Pacific Journal of Cancer Prevention | 2014

Mitochondria-mediated Apoptosis in Human Lung Cancer A549 Cells by 4-Methylsulfinyl-3-butenyl Isothiocyanate from Radish Seeds

Nan Wang; Wei Wang; Po Huo; Caiqin Liu; Jianchang Jin; Lianqing Shen

4-Methylsulfinyl-3-butenyl isothiocyanate (MTBITC) found in the radish (Raphanus sativus L.), is a well- known anticancer agent. In this study, the mechanisms of the MTBITC induction of cell apoptosis in human A549 lung cancer cells were investigated. Our PI staining results showed that MTBITC treatment significantly increased the apoptotic sub-G1 fraction in a dose-dependent manner. The mechanism of apoptosis induced by MTBITC was investigated by testing the change of mitochondrial membrane potential (Δψm), the expression of mRNAs of apoptosis-related genes by RT-PCR, and the activities of caspase-3 and -9 by caspase colorimetric assay. MTBITC treatment decreased mitochondrial membrane potential by down-regulating the rate of Bcl-2/ Bax and Bcl-xL/Bax, and activation of caspase-3 and -9. Therefore, mitochondrial pathway and Bcl-2 gene family could be involved in the mechanisms of A549 cell apoptosis induced by MTBITC.


Journal of Chemical Research-s | 2010

A new abietane diterpenoid from Clerodendrum kaichianum Hsu

Mingfeng Xu; Lianqing Shen; Kuiwu Wang; Qizhen Du

A new abietane diterpenoid has been isolated from Clerodendrum kaichianum Hsu and characterised as 11-methoxyl-12,14-dihydroxy-13-(2-hydroxypropyl)-3,5,8,11,13-abietapentaen-7-one. Its structure was established by spectroscopic analysis, including 2D NMR.


Journal of the Science of Food and Agriculture | 2016

Inhibition of Growth and Induction of Apoptosis in A549 Cells by Compounds from Oxheart Cabbage Extract

Nan Wang; Wei Wang; Caiqin Liu; Jianchang Jin; Bo Shao; Lianqing Shen

BACKGROUND Oxheart cabbage (Brassica oleracea var. capitata) is a member of the Brassica genus. Although some studies on the anticancer effects of extracts from oxheart cabbage have been reported, comprehensive information on the bioactive fractions and components from oxheart cabbage extracts is still lacking. The aim of this study was to isolate and identify the bioactive fractions and components from oxheart cabbage seeds using activity-guided isolation methods. RESULTS The cytotoxicity and apoptotic effects of fraction II, fraction III, iberverin, sulforaphane and iberin from oxheart cabbage seed extract were investigated. The results showed that all five components had inhibitory effects on the in vitro growth of A549 cells which were dose-dependent. These compounds also changed the morphology of A549 cells, and their inhibitory activity on A549 cells was as follows: sulforaphane > iberin > iberverin > fraction III > fraction II. The IC50 values were 3.53 ± 0.63, 4.93 ± 1.02, 7.07 ± 0.51, 15.56 ± 0.24 and 27.32 ± 0.63 µg mL(-1) respectively. Fraction II, fraction III, iberverin, sulforaphane and iberin induced cell apoptosis by increasing early apoptosis and late apoptosis/necrosis, and activation of caspase-3, -8 and -9. CONCLUSION These results indicated that the decrease in A549 cell viability by active compounds from oxheart cabbage seed extract was due to the induction of apoptosis.


Food Chemistry | 2008

Studies on tea protein extraction using alkaline and enzyme methods

Lianqing Shen; Xiangyang Wang; Zhongying Wang; Yuanfeng Wu; Jianshe Chen


Food Chemistry | 2010

Endogenous and exogenous enzymolysis of vegetable-sourced glucosinolates and influencing factors.

Lianqing Shen; Guang‐yao Su; Xiangyang Wang; Qizhen Du; Kuiwu Wang


Helvetica Chimica Acta | 2011

Two New Abietane Diterpenoids from the Stems of Clerodendrum kaichianum P. S. Hsu

Mingfeng Xu; Lianqing Shen; Kuiwu Wang; Qizhen Du


Archive | 2009

Double-enzyme extraction method of tea protein

Lianqing Shen; Zhongying Wang; Guangrong Huang; Yuanfeng Wu; Po Huo


Archive | 2012

Method for separating and preparing Liriope graminifolia saponin A from Liriope graminifolia

Lianqing Shen; Kuiwu Wang; Wei Wang

Collaboration


Dive into the Lianqing Shen's collaboration.

Top Co-Authors

Avatar

Kuiwu Wang

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Qizhen Du

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Hong Zhang

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Mingfeng Xu

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Wei Wang

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Xiangyang Wang

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Yuanfeng Wu

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Zhongying Wang

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Guang‐yao Su

Zhejiang Gongshang University

View shared research outputs
Top Co-Authors

Avatar

Jianrong Li

Zhejiang Gongshang University

View shared research outputs
Researchain Logo
Decentralizing Knowledge