P. Dung

发表

New benzothiazole/thiazole-containing hydroxamic acids as potent histone deacetylase inhibitors and antitumor agents.

J. Hong, B. Han, S. H. Park, 2013, Medicinal chemistry (Shariqah (United Arab Emirates)).

Design, synthesis, and evaluation of novel (E)‐N'‐(3‐allyl‐2‐hydroxy)benzylidene‐2‐(4‐oxoquinazolin‐3(4H)‐yl)acetohydrazides as antitumor agents

S. Han, T. Tung, P. Dung, 2021, Archiv der Pharmazie.

Design, Synthesis and Evaluation of Novel Indirubin-based N-Hydroxybenzamides, N-Hydroxypropenamides and N-Hydroxyheptanamides as Histone Deacetylase Inhibitors and Antitumor Agents.

S. Han, T. Tung, P. Dung, 2020, Bioorganic & medicinal chemistry letters.

Quinazoline‐Based Hydroxamic Acids: Design, Synthesis, and Evaluation of Histone Deacetylase Inhibitory Effects and Cytotoxicity

S. Han, P. Dung, N. Nam, 2018, Chemistry & biodiversity.

Design, synthesis and evaluation of novel N-hydroxybenzamides/N-hydroxypropenamides incorporating quinazolin-4(3H)-ones as histone deacetylase inhibitors and antitumor agents.

S. Han, P. Dung, N. Nam, 2018, Bioorganic chemistry.

Novel 2-oxoindoline-based hydroxamic acids: synthesis, cytotoxicity, and inhibition of histone deacetylation

B. Han, S. Han, P. Dung, 2015 .

Novel isatin-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents.

B. Han, S. H. Park, S. Han, 2013, European journal of medicinal chemistry.

Synthesis and biological evaluation of a series of 2-(substitutedphenyl)benzothiazoles.

P. Thuong, P. Dung, N. Nam, 2011, Medicinal chemistry (Shariqah (United Arab Emirates)).

Exploration of some indole-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents

P. Huong, S. Han, P. Dung, 2017, Chemical Papers.

2-Aryl- and 2-amido-benzothiazoles as multifunctional vasodilators on rat artery preparations.

F. Fusi, N. Cuong, P. Dung, 2013, European journal of pharmacology.

Synthesis and bioevaluation of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety

B. Han, S. Han, P. Dung, 2015, Medicinal Chemistry Research.

5-aryl-1,3,4-thiadiazole-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents: synthesis, bioevaluation and docking study.

B. Han, S. Han, Youngsoo Kim, 2015, Medicinal chemistry (Shariqah (United Arab Emirates)).

Synthesis, bioevaluation and docking study of 5-substitutedphenyl-1,3,4-thiadiazole-based hydroxamic acids as histone deacetylase inhibitors and antitumor agents

B. Han, S. Han, Youngsoo Kim, 2014, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and bioevaluation of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety

S. Han, Youngsoo Kim, P. Dung, 2015, Medicinal Chemistry Research.

Exploration of novel 5′(7′)-substituted-2′-oxospiro[1,3]dioxolane-2,3′-indoline-based N-hydroxypropenamides as histone deacetylase inhibitors and antitumor agents

B. Han, S. Han, P. Dung, 2017 .