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Zhongguo Fei AI Za Zhi = Chinese Journal of Lung Cancer|January 12, 2025
[Non-small Cell Lung Cancer Cell Line PC-9 Drug-resistant Mutant Cell Line Establishment and Validation of Their Sensitivity to EGFR Inhibitors]Tao Hu, Yang Lou, Mingbo Su
Molecules (Basel, Switzerland)|June 6, 2013
The design and synthesis of a new class of RTK/HDAC dual-targeted inhibitorsXuan Zhang, Mingbo Su, Yi Chen, et al.
Expert Opinion on Therapeutic Patents|August 18, 2025
A patent review of CHK1 inhibitors (2019 - present)Tao Liu, Mingbo Su, Yuxuan Wang, et al.
Chemical Biology & Drug Design|June 26, 2012
Discovering novel α-aminoacyl-containing proline derivatives with potent and selective inhibitory activity against dipeptidyl peptidase IV: design, synthesis, biological evaluation, and molecular modelingXiaodong Zhang, Jiang Wang, Mingbo Su, et al.
Chemical Biology & Drug Design|September 22, 2012
Design, synthesis, structure-activity relationships, and docking studies of 1-(γ-1,2,3-triazol substituted prolyl)-(S)-3,3-difluoropyrrolidines as a novel series of potent and selective dipeptidyl peptidase-4 inhibitorsLei Zhang, Mingbo Su, Jingya Li, et al.
Bioorganic & Medicinal Chemistry|December 3, 2014
(R)-3-amino-1-((3aS,7aS)-octahydro-1H-indol-1-yl)-4-(2,4,5-trifluorophenyl)butan-1-one derivatives as potent inhibitors of dipeptidyl peptidase-4: design, synthesis, biological evaluation, and molecular modelingSinan Wang, Mingbo Su, Jiang Wang, et al.
Organic Letters|April 24, 2012
Streptocarbazoles A and B, two novel indolocarbazoles from the marine-derived actinomycete strain Streptomyces sp. FMAPeng Fu, Chunli Yang, Yi Wang, et al.
Bioorganic & Medicinal Chemistry|September 29, 2014
Design, synthesis and biological evaluation of 4-anilinothieno[2,3-d]pyrimidine-based hydroxamic acid derivatives as novel histone deacetylase inhibitorsWei Yang, Lixuan Li, Xun Ji, et al.
European Journal of Medicinal Chemistry|February 19, 2017
Design, synthesis and biological evaluation of thienopyrimidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitorsJiang Wang, Mingbo Su, Tingting Li, et al.
Bioorganic & Medicinal Chemistry|August 18, 2018
A series of camptothecin prodrugs exhibit HDAC inhibition activityQiwen Zhu, Xumeng Yu, Qianqian Shen, et al.
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