Xiao-Ya Shang

Dr. Xiao-Ya Shang

Beijing Union University

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2021 in Food Chemistry
Verified
Journal Article
Closed access
XZXiangjian Zhong
Xiangjian Zhong
XWXin Wang
Xin Wang
NZNa Zhou
Na Zhou
JLJinjie Li
Jinjie Li
JLJiachen Liu
Jiachen Liu
XSXiao-Ya Shang
Xiao-Ya Shang

1 March 2020 in Food Chemistry
Verified
Journal Article
Closed access
YZYunping Zhu
Yunping Zhu
XSXiao-Ya Shang
Xiao-Ya Shang
LYLi Yang
Li Yang
SZShenglan Zheng
Shenglan Zheng
KLKaifeng Liu
Kaifeng Liu
XLXiuting Li
Xiuting Li

11 February 2019 in Molecules
Verified
Journal Article
Open access
PDF file
LJLin-Lin Ji
Lin-Lin Ji
XWXin Wang
Xin Wang
JLJinjie Li
Jinjie Li
XZXINAG JIAN ZHONG
XINAG JIAN ZHONG
BZBo Zhang
Bo Zhang
XSXiao-Ya Shang
Xiao-Ya Shang
Three previously undescribed iridoids, cornusfurals A–C, were isolated from the ethanolic extracts of fruits of Cornus officinalis. Their structures were elucidated by spectroscopic methods, including one-dimensional and two-dimensional nuclear magnetic resonance, ultraviolet spectroscopy, infrared spectroscopy, and mass spectrometry. The neuroprotective activity was evaluated by measuring corticosterone-induced damage in PC12 cells. The results showed that cornusfural B decreased corticosterone-induced PC12 cell damage compared with that in model cells.

10 May 2013 in Journal of Asian Natural Products Research
Verified
Journal Article
Closed access
MLMing-Tao Liu
Ming-Tao Liu
AWA-Li Wang
A-Li Wang
ZSZhen Sun
Zhen Sun
JLJin-Jie Li
Jin-Jie Li
XWXiu-Li Wu
Xiu-Li Wu
XSXiao-Ya Shang
Xiao-Ya Shang
Two new monacolin analogs, monacolins O (1) and P (2), along with three known analogs, have been isolated from the ethanolic extract of Monascus purpureus-fermented rice. Their structures and absolute configurations were elucidated by spectroscopic methods, especially 2D NMR and CD spectral analyses as well as chemical method. Both 1 and 2 were tested against five tumor cell lines, and compound 1 exhibited selective cytotoxic activity against A2780 and A549 cell lines, with IC50 values of 3.7 and 8.0 μM, respectively.

27 December 2016 in Journal of Natural Products
Verified
Journal Article
Closed access
WWWendi Wei
Wendi Wei
SLSheng Lin
Sheng Lin
MCMinghua Chen
Minghua Chen
TLTianxi Liu
Tianxi Liu
AWAli Wang
Ali Wang
XSXiao-Ya Shang
Xiao-Ya Shang

18 February 2020 in Molecules
Verified
Journal Article
Open access
PDF file
XWXin Wang
Xin Wang
XZXINAG JIAN ZHONG
XINAG JIAN ZHONG
NZNa Zhou
Na Zhou
NCNing Cai
Ning Cai
JXJia-Hui Xu
Jia-Hui Xu
XSXiao-Ya Shang
Xiao-Ya Shang
Gymnadenia conopsea R. Br. is a traditional Tibetan medicinal plant that grows at altitudes above 3000 m, which is used to treat neurasthenia, asthma, coughs, and chronic hepatitis. However, a comprehensive configuration of the chemical profile of this plant has not been reported because of the complexity of its chemical constituents. In this study, a rapid and precise method based on ultra-high performance liquid chromatography (UPLC) combined with an Orbitrap mass spectrometer (UPLC–Orbitrap–MS/MS) was established in both positive- and negative-ion modes to rapidly identify various chemical components in the tubers of G. conopsea for the first time. Finally, a total of 91 compounds, including 17 succinic acid ester glycosides, 9 stilbenes, 6 phenanthrenes, 19 alkaloids, 11 terpenoids and steroids, 20 phenolic acid derivatives, and 9 others, were identified in the tubers of G. conopsea based on the accurate mass within 3 ppm error. Furthermore, many alkaloids, phenolic acid derivates, and terpenes were reported from G. conopsea for the first time. This rapid method provides an important scientific basis for further study on the cultivation, clinical application, and functional food of G. conopsea.