Guoping Zhou

Guoping Zhou


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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25 June 2017 in Journal of Asian Natural Products Research
Verified
Journal Article
Closed access
HFHui-Zheng Fu
Hui-Zheng Fu
KWKai-Hua Wan
Kai-Hua Wan
QYQing-Wei Yan
Qing-Wei Yan
GZGuoping Zhou
Guoping Zhou
TFTong-Tong Feng
Tong-Tong Feng
RZRui-Jian Zhong
Rui-Jian Zhong
Five new oleanane-type triterpenoid saponins, oleiferasaponins D1–D5 (1–5), were isolated from the defatted seeds of Camellia oleifera Abel. Their structures were elucidated by spectroscopic and chemical methods. The cytotoxic activities of compounds 1–5 were evaluated against five human tumor cell lines (HCT-116, HepG2, BGC-823, NCI-H1650, and A2780). Compounds 1–2 exhibited cytotoxic activity against five human cancer cell lines, with IC50 values ranging from 3.31 to 10.23 μM. Compounds 3–5 showed moderate cytotoxic activities toward the tested cell lines.

19 May 2015 in Molecules
Verified
Journal Article
Open access
PDF file
GZGuoping Zhou
Guoping Zhou
YYYan Yu
Yan Yu
MYMingming Yuan
Mingming Yuan
Ji TengfeiJi Tengfei
Ji Tengfei
HFHuizheng Fu
Huizheng Fu
RZRui-Jian Zhong
Rui-Jian Zhong
Four new triterpenoids which were identifed as 2α,3β,6β,19α-tetrahydroxy- oleanolic acid 28-O-β-D-glucopyranoside (1), 2-O-β-D-glucopyranosyloxy-3α,19α-di-hydroxyoleanolic acid (2), 2-O-β-D-glucopyranosyloxy-3α,19α-dihydroxyursolic acid (3), 2α,3α,6β,19α-tetrahydroxyursolic acid 28-O-β-D-glucopyranoside (4), were isolated from the aerial parts of Callicarpa kwangtungensis together with three known triterpenoids identified as 2α,3β,21β-trihydroxyursolic acid 28-O-β-D-glucopyranoside (5), 2α,3α,19α,23-tetrahydroxyoleanolic acid 28-O-β-D-glucopyranoside (6), 2α,3α,19α,23-tetrahydroxyursolic acid 28-O-β-D-glucopyranoside (7). Their structures were elucidated by the combination of mass spectrometry (MS), one and two-dimensional NMR experiments.

31 October 2014 in Journal of Asian Natural Products Research
Verified
Journal Article
Closed access
MYMing-Ming Yuan
Ming-Ming Yuan
RZRui-Jian Zhong
Rui-Jian Zhong
GCGang Chen
Gang Chen
GZGuoping Zhou
Guoping Zhou
HFHui-Zheng Fu
Hui-Zheng Fu
QYQing-Wei Yan
Qing-Wei Yan
Two new triterpenoids, 2α,3β,16α,19α,23-pentahydroxyolean-12-en-28-oic acid (1) and 2α,3α,11α,21α,23-pentahydroxyurs-12-en-28-oic acid (2), were isolated from the aerial parts of Callicarpa kwangtungensis. Their structures were elucidated by 1D and 2D analyses, as well as MS and IR spectra.

1 February 2010 in Journal of Asian Natural Products Research
Verified
Journal Article
Closed access
DWDong Wang
Dong Wang
JTJin Tian
Jin Tian
GZGuoping Zhou
Guoping Zhou
YYYi-Sheng Yang
Yi-Sheng Yang
YSYa-Lun Su
Ya-Lun Su
Ji TengfeiJi Tengfei
Ji Tengfei
A new bidesmoside triterpenoid saponin, named stauntoside C1 (1), along with three known saponins (2–4) was isolated from Stauntonia chinensis DC. (Lardizabalaceae). Their structures were established by means of spectral and chemical methods as 3-O-β-d-xylopyranosyl-(1 → 2)-O-β-d-xylopyranosyl-(1 → 3)-O-α-l-rhamnopyranosyl-(1 → 2)-α-l-arabinopyranosyl oleanolic acid 28-O-α-l-rhamnopyranosyl-(1 → 4)-β-d-glucopyranosyl-(1 → 6)-β-d-glucopyranosyl ester (1), scabiosaponin E (2), sieboldianoside B (3), and kizutasaponin K12 (4).

17 May 2019 in Biomedical Chromatography
Verified
Journal Article
Closed access
PDF file
WCWeikang Chen
Weikang Chen
YZYangbin Zheng
Yangbin Zheng
LYLiang Yan
Liang Yan
MYMingming Yuan
Mingming Yuan
LOLan Ouyang
Lan Ouyang
RZRuijian Zhong
Ruijian Zhong

4 January 2017 in Biomedical Chromatography
Verified
Journal Article
Closed access
PDF file
RZRuijian Zhong
Ruijian Zhong
YYYan Yu
Yan Yu
YZYangbing Zheng
Yangbing Zheng
WCWeikang Chen
Weikang Chen
GZGuoping Zhou
Guoping Zhou
MYMingming Yuan
Mingming Yuan