Wei-Ming Zhou
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Wei-Ming Zhou has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
Bingren Xiang
China Pharmaceut Univ, Nanjing 210009, Jiangsu, Peoples R China
1 shared publication- De-Yu Liu
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China
1 shared publication Dong Ying
China Pharmaceut Univ, Nanjing 210009, Jiangsu, Peoples R China
1 shared publication- Hao Liu
Department of Pharmacy, Guangdong Food and Drug Vocational College, Guangzhou 510520, China
1 shared publication - Jiantao Ye
School of Pharmaceutical Sciences, Sun Yat-Sen University, National and Local United Engineering Lab of Druggability and New Drugs Evaluation, Guangdong Provincial Key Laboratory of New Drug Design and Evaluation, Guangzhou, China
1 shared publication - Na Zhang
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China
1 shared publication
Latest Publications
- 1 April 2019
- Published by Elsevier in Journal of Molecular Structure
- Vol. 1181, 436-443
Generalized two-dimensional correlation NIR spectroscopy analysis of the structures on n-propanol and n-butanol
- 1 April 2019
- Published by Elsevier in Journal of Molecular Structure
- Vol. 1181, 436-443
Generalized two-dimensional correlation NIR spectroscopy analysis of the structures on n-propanol and n-butanol
- Open Access
Synthesis and Biological Evaluation of New 5-Fluorouracil-Substituted Ampelopsin Derivatives
This study reports two novel 5-fluorouracil-substituted ampelopsin derivatives. The structures of two new derivatives were characterized by elemental analysis, 1H-NMR, 13C-NMR, IR and MS. Their anticancer activities in vitro against two cancer cell lines, K562 and K562/ADR, were investigated using the MTT assay, and the results showed that the two new compounds were more effective than reference drugs such as ampelopsin and verapamil.
Open AccessSynthesis and Biological Evaluation of New 5-Fluorouracil-Substituted Ampelopsin Derivatives
This study reports two novel 5-fluorouracil-substituted ampelopsin derivatives. The structures of two new derivatives were characterized by elemental analysis, 1H-NMR, 13C-NMR, IR and MS. Their anticancer activities in vitro against two cancer cell lines, K562 and K562/ADR, were investigated using the MTT assay, and the results showed that the two new compounds were more effective than reference drugs such as ampelopsin and verapamil.