Junwei Wang

发表

Efficient construction of novel D-ring modified steroidal dienamides and their cytotoxic activities.

Xiao-Jing Shi, Hong-min Liu, E. Zhang, 2013, European journal of medicinal chemistry.

Design, synthesis, and structure-activity relationship of novel LSD1 inhibitors based on pyrimidine-thiourea hybrids as potent, orally active antitumor agents.

Zhijia Wang, Lina Ding, Liying Ma, 2015, Journal of medicinal chemistry.

Generation and characterization of a paclitaxel-resistant human gastric carcinoma cell line

F. Yin, Hong-min Liu, Bing Han, 2018, Anti-cancer drugs.

Structurally novel steroidal spirooxindole by241 potently inhibits tumor growth mainly through ROS-mediated mechanisms

Xiao-Jing Shi, Hong-min Liu, Bin Yu, 2016, Scientific Reports.

Discovery of novel tertiary amide derivatives as NEDDylation pathway activators to inhibit the tumor progression in vitro and in vivo.

Dongjun Fu, Ting Zhu, Yan-Bing Zhang, 2020, European journal of medicinal chemistry.

The Antitumor Activity of the Novel Compound Jesridonin on Human Esophageal Carcinoma Cells

Y. Liu, Yu Ke, Cong Wang, 2015, PloS one.

Anti-proliferative effect of Jesridonin on paclitaxel-resistant EC109 human esophageal carcinoma cells

Yu Ke, Cong Wang, Ran Wang, 2017, International journal of molecular medicine.

JD enhances the anti-tumour effects of low-dose paclitaxel on gastric cancer MKN45 cells both in vitro and in vivo

Y. Liu, Yu Ke, Ran Wang, 2016, Cancer Chemotherapy and Pharmacology.

Multicomponent assembly of novel antiproliferative steroidal dihydropyridinyl spirooxindoles

Yan-ling Zhang, Hong-min Liu, Bin Yu, 2016, Steroids.

Synthesis, in vitro and in vivo anticancer activities of novel 4-substituted 1,2-bis(4-chlorophenyl)-pyrazolidine-3,5-dione derivatives

Wen-en Zhao, Hong-min Liu, Kun-Peng Shao, 2015 .

Inhibition of lysine-specific demethylase 1 enhances the sensitivity of the chemotherapeutic drug doxorubicin in gastric cancer cell

Wen-en Zhao, Junwei Wang, Hong-Min Liu, 2022, Molecular Biology Reports.

Structure-Activity Relationship Studies of β-Lactam-azide Analogues as Orally Active Antitumor Agents Targeting the Tubulin Colchicine Site

B. Zhao, Dongjun Fu, Yan-Bing Zhang, 2017, Scientific Reports.

D-ring modified novel isosteviol derivatives: design, synthesis and cytotoxic activity evaluation.

Tao Zhang, Hao Liu, Junwei Wang, 2012, Bioorganic & medicinal chemistry letters.

Triazole-dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration.

D. Mobley, Wen-en Zhao, X. Zi, 2013, Journal of medicinal chemistry.