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2. Design, synthesis and bioevaluation of novel N-heterocyclic hydroxamic acids as histone deacetylase inhibitors and their antitumor activity study.

3. Correction: Novel (E)-3-(1-substituted-1H-indazol-5-yl)-N-hydroxypropenamides as histone deacetylase inhibitors: design, synthesis and structure–activity relationships

6. Determination of drug-related problems among type 2 diabetes outpatients in a hospital in Vietnam: A cross-sectional study

7. Novel (E)‐3‐(3‐oxo‐4‐substituted‐3,4‐dihydro‐2H‐benzo[b][1,4]oxazin‐6‐yl)‐N‐hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis and Bioevaluation

8. Novel (E)-3-(1- substituted-1H-indazol-5-yl)-N-hydroxypropenamides as Histone Deacetylase Inhibitors: Design, Synthesis and Structure-Activity Relationships

9. Identification of novel phenylalanine derivatives bearing a hydroxamic acid moiety as potent quorum sensing inhibitorsElectronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3md00670k

11. Benzo[d]thiazole-2-thiol bearing 2-oxo-2-substituted-phenylethan-1-yl as potent selective lasB quorum sensing inhibitors of Gram-negative bacteria

13. Fusaric acid and derivatives as novel antimicrobial agents

14. Drug Discovery and Development on Pma1, Where Are We Now? A Critical Review from 1995 to 2022

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24. The beneficial role of FeNO in association with GINA guidelines for titration of inhaled corticosteroids in adult asthma: A randomized study

25. Multi-indicators Multi-objective Evolutionary Algorithm with Q-Learning for Real-world Network Optimization

26. "Left-hand strategy" for the design, synthesis and discovery of novel triazole–mercaptobenzothiazole hybrid compounds as potent quorum sensing inhibitors and anti-biofilm formation of Pseudomonas aeruginosa.

28. Correction: Benzo[d]thiazole-2-thiol bearing 2-oxo-2-substituted-phenylethan-1-yl as potent selective lasB quorum sensing inhibitors of Gram-negative bacteria

29. Antimicrobial peptides – Advances in development of therapeutic applications

30. Resolving Micro-grid Energy Optimization Using Multi-objective Artificial Bee Colony Algorithm

31. Design, synthesis, and evaluation of novel N'-substituted-1-(4-chlorobenzyl)-1H-indol-3-carbohydrazides as antitumor agents

33. Cover Feature: LEGO-Inspired Drug Design: Unveiling a Class of Benzo[d ]thiazoles Containing a 3,4-Dihydroxyphenyl Moiety as Plasma Membrane H+ -ATPase Inhibitors (ChemMedChem 1/2018)

39. 2-Difluoromethylpyridine as a bioisosteric replacement of pyridine-N-oxide: the case of quorum sensing inhibitorsElectronic supplementary information (ESI) available. See DOI: 10.1039/d1md00245g

40. LEGO-inspired drug design: Discovery of novel fungal Plasma membrane H+-ATPase (Pma1) inhibitors from small molecule libraries: An introduction of HFSA-SBS_DOS-RD strategy in drug discovery.

41. Perturbing dissimilar biomolecular targets from natural product scaffolds and focused chemical decoration.

46. Metformin, an Anthropogenic Contaminant of Seidlitzia rosmarinusCollected in a Desert Region near the Gulf of Aqaba, Sinai Peninsula

48. Design, Synthesis and Evaluation of Novel (E)-N'-((1-(4-chlorobenzyl)-1H-indol-3-yl)methylene)-2-(4-oxoquinazolin-3(4H)-yl)acetohydrazides as Antitumor Agents.

49. Comparison between Three Techniques for Determining Glomerular Filtration Rates: 99m Tc-Diethylene Triamine Penta-Acetic Acid Renography, Double Plasma Sampling Method, and Single Plasma Sampling Method in Vietnamese Patients.

50. LEGO-Inspired Drug Design: Unveiling a Class of Benzo[d]thiazoles Containing a 3,4-Dihydroxyphenyl Moiety as Plasma Membrane H + -ATPase Inhibitors.

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