Supaporn Seetaha

发表

Synthesis, HIV-1 RT inhibitory, antibacterial, antifungal and binding mode studies of some novel N-substituted 5-benzylidine-2,4-thiazolidinediones

K. Choowongkomon, S. Ganguly, R. S. Bahare, 2015, DARU Journal of Pharmaceutical Sciences.

Discovery of New and Potent InhA Inhibitors as Anti-tuberculosis Agents: Structure Based Virtual Screening Validated by Biological Assays and X-ray Crystallography. Journal of Chemical Information and Modeling, 60 (2020)(1), 226-234.

Rosemary A Blood, P. Srimanote, S. Hannongbua, 2020 .

Application of Site‐Specific Spin Labeling for NMR Detecting Inhibitor‐Induced Conformational Change of HIV‐1 Reverse Transcriptase

Takumi Yamaguchi, Koichi Kato, M. Yagi-Utsumi, 2016, ChemMedChem.

Synthesis, evaluation and binding mode analysis of some novel triazole derivatives as antimicrobials

K. Sen, Subhasis Banerjee, K. Choowongkomon, 2013 .

Synthesis, HIV-1 RT inhibitory, antibacterial, antifungal and binding mode studies of some novel N-substituted 5-benzylidine-2,4-thiazolidinediones

K. Choowongkomon, S. Ganguly, R. S. Bahare, 2015, DARU Journal of Pharmaceutical Sciences.

Anti-HIV-1 reverse transcriptase activities of hexane extracts from some Asian medicinal plants

S. Hannongbua, K. Silprasit, K. Choowongkomon, 2011 .

Computational screening of chalcones acting against topoisomerase IIα and their cytotoxicity towards cancer cell lines

T. Rungrotmongkol, P. Wolschann, N. Kungwan, 2018, Journal of Enzyme Inhibition and Medicinal Chemistry.

Ecological effects on food utilization, trypsin isozymes, and performance qualities of growth and maturation in Northeast Arctic cod (Gadus morhua L.)

K. Thongprajukaew, U. Kovitvadhi, K. Choowongkomon, 2012 .

Discovery of potent antiproliferative agents from selected oxygen heterocycles as EGFR tyrosine kinase inhibitors from the U.S. National Cancer Institute database by in silico screening and bioactivity evaluation.

K. Choowongkomon, S. Ruchirawat, Chatchakorn Eurtivong, 2022, Bioorganic & medicinal chemistry letters.

Discovery of New and Potent InhA Inhibitors as Antituberculosis Agents: Structure-Based Virtual Screening Validated by Biological Assays and X-ray Crystallography

Pharit Kamsri, Chayanin Hanwarinroj, Naruedon Phusi, 2019, J. Chem. Inf. Model..

Disassembly of the self-assembled, double-ring structure of proteasome α7 homo-tetradecamer by α6

Koichi Kato, Kentaro Ishii, H. Yagi, 2015, Scientific Reports.

Disassembly of the self-assembled, double-ring structure of proteasome alpha 7 homo-tetradecamer by alpha 6

Koichi Kato, Kentaro Ishii, H. Yagi, 2015 .