Yu Wang

Mrs. Yu Wang


Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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28 December 2015 in Molecules
Verified
Journal Article
Open access
PDF file
YWYu Wang
Yu Wang
DLDahong Li
Dahong Li
ZLZhan-Lin Li
Zhan-Lin Li
YSYanjun Sun
Yanjun Sun
HHHui-Ming Hua
Hui-Ming Hua
JBJiao Bai
Jiao Bai
Two new β-bergamotane sesquiterpenoids, E-β-trans-5,8,11-trihydroxybergamot-9-ene (1) and β-trans-2β,5,15-trihydroxybergamot-10-ene (2), were isolated from the marine-derived fungus Aspergillus fumigatus YK-7, along with three known terpenoids 3–5. Their structures were determined by spectroscopic methods (1D and 2D NMR, HR-ESI-MS). Antiproliferative effects on human leukemic monocyte lymphoma U937 and human prostate cancer PC-3 cell lines were measured in vitro. Compound 4 exhibited potent activity against the U937 cell line with an IC50 value of 4.2 μM.

31 March 2016 in Molecules
Verified
Journal Article
Open access
PDF file
YSYanjun Sun
Yanjun Sun
MGMei-Ling Gao
Mei-Ling Gao
YZYan-Li Zhang
Yan-Li Zhang
JWJun-Min Wang
Jun-Min Wang
YWYa Wu
Ya Wu
TLTao Liu
Tao Liu
Two new labdane diterpenes, sinoditerpene A (1) and B (2), were isolated from the fruits of Sinopodophyllum emodi, along with two known analogues 3 and 4. Their structures were established on the basis of extensive spectroscopic analysis. The isolation of compounds 1–4 represents the first report of diterpenes from the genus Sinopodophyllum. The cytotoxic activities of all isolated compounds were evaluated in comparison with 5-fluorouracil against the MCF-7 and HepG2 cell lines, towards which 3 showed more potent cytotoxicity.

26 May 2015 in Molecules
Verified
Journal Article
Open access
PDF file
YSYanjun Sun
Yanjun Sun
YZYan-Li Zhang
Yan-Li Zhang
YWYu Wang
Yu Wang
JWJun-Min Wang
Jun-Min Wang
XZXuan Zhao
Xuan Zhao
YGYan-Bin Guan
Yan-Bin Guan
In the present work, a quantitative 1H Nuclear Magnetic Resonance (qHNMR) was established for purity assessment of six aryltetralin lactone lignans. The validation of the method was carried out, including specificity, selectivity, linearity, accuracy, precision, and robustness. Several experimental parameters were optimized, including relaxation delay (D1), scan numbers (NS), and pulse angle. 1,4-Dinitrobenzene was used as internal standard (IS), and deuterated dimethyl sulfoxide (DMSO-d6) as the NMR solvent. The purities were calculated by the area ratios of H-2,6 from target analytes vs. aromatic protons from IS. Six aryltetralin lactone lignans (deoxypodophyllotoxin, podophyllotoxin, 4-demethylpodophyllotoxin, podophyllotoxin-7′-O-β-d-glucopyranoside, 4-demethylpodophyllotoxin-7′-O-β-d-glucopyranoside, and 6′′-acetyl-podophyllotoxin-7′-O-β -d-glucopyranoside) were analyzed. The analytic results of qHNMR were further validated by high performance liquid chromatography (HPLC). Therefore, the qHNMR method was a rapid, accurate, reliable tool for monitoring the purity of aryltetralin lactone lignans.