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Supa Hannongbua

Explore the profile of Supa Hannongbua including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 117
Citations 454
Followers 0
Related Specialties
Chemistry
Biochemistry
Molecular Biology
Top 10 Co-Authors
Patchreenart Saparpakorn
Kiattawee Choowongkomon
Pornpan Pungpo
Auradee Punkvang
M Paul Gleeson
Pharit Kamsri
Peter Wolschann
James Spencer
Songwut Suramitr
Adrian J Mulholland
Published In
J Mol Graph Model
J Mol Model
J Chem Inf Model
Molecules
Chem Biol Interact
Affiliations
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Recent Articles
1.
Role of interaction mode of phenanthrene derivatives as selective PDE5 inhibitors using molecular dynamics simulations and quantum chemical calculations
Sainimnuan S, Chimprasit A, Hannongbua S, Saparpakorn P
Mol Divers . 2024 Jul; 29(2):1683-1696. PMID: 39080154
Phosphodiesterase type 5 (PDE5) inhibitors play a crucial role in blocking PDE5 to improve erectile dysfunction (ED). However, most PDE5 drugs revealed side effects including the loss of vision due...
2.
Ligand-Based Virtual Screening for Discovery of Indole Derivatives as Potent DNA Gyrase ATPase Inhibitors Active against and Hit Validation by Biological Assays
Pakamwong B, Thongdee P, Kamsri B, Phusi N, Taveepanich S, Chayajarus K, et al.
J Chem Inf Model . 2024 Jul; 64(15):5991-6002. PMID: 38993154
is the single most important global infectious disease killer and a World Health Organization critical priority pathogen for development of new antimicrobials. DNA gyrase is a validated target for anti-TB...
3.
Signal Propagation in the ATPase Domain of DNA Gyrase from Dynamical-Nonequilibrium Molecular Dynamics Simulations
Kamsri B, Kamsri P, Punkvang A, Chimprasit A, Saparpakorn P, Hannongbua S, et al.
Biochemistry . 2024 May; 63(11):1493-1504. PMID: 38742407
DNA gyrases catalyze negative supercoiling of DNA, are essential for bacterial DNA replication, transcription, and recombination, and are important antibacterial targets in multiple pathogens, including , which in 2021 caused...
4.
3D-QSAR and molecular docking studies of peptide-hybrids as dengue virus NS2B/NS3 protease inhibitors
Jitonnom J, Meelua W, Tue-Nguen P, Saparpakorn P, Hannongbua S, Chotpatiwetchkul W
Chem Biol Interact . 2024 May; 396:111040. PMID: 38735453
Global warming and climate change have made dengue disease a global health issue. More than 50 % of the world's population is at danger of dengue virus (DENV) infection, according...
5.
Comparison of feline and human immunodeficiency virus reverse transcriptase enzymes through chemical screening and computational analysis
Thammajong P, Aiebchun T, Boonyarattanakalin K, Gleeson D, Pobsuk N, Hannongbua S, et al.
Chem Biol Drug Des . 2024 May; 103(5):e14530. PMID: 38725091
Feline immunodeficiency virus (FIV) is a common infection found in domesticated and wild cats worldwide. Despite the wealth of therapeutic understanding of the disease in humans, considerably less information exists...
6.
Combining Deep Learning and Structural Modeling to Identify Potential Acetylcholinesterase Inhibitors from
Sutthibutpong T, Posansee K, Liangruksa M, Termsaithong T, Piyayotai S, Phitsuwan P, et al.
ACS Omega . 2024 Apr; 9(14):16311-16321. PMID: 38617639
Alzheimer's disease (AD) is the most common type of dementia, affecting over 50 million people worldwide. Currently, most approved medications for AD inhibit the activity of acetylcholinesterase (AChE), but these...
7.
Binding interactions and in silico ADME prediction of isoconessimine derivatives as potent acetylcholinesterase inhibitors
Tue-Ngeun P, Rakitikul W, Thinkumrob N, Hannongbua S, Meelua W, Jitonnom J
J Mol Graph Model . 2024 Feb; 129:108746. PMID: 38401250
In pursuit of new acetylcholinesterase (AChE) inhibitors for treating Alzheimer's disease (AD), a series of ten previously synthesized isoconessimine compounds (7a-7j) was in silico investigated for their binding interactions with...
8.
Combined Deep Learning and Molecular Modeling Techniques on the Virtual Screening of New mTOR Inhibitors from the Thai Mushroom Database
Posansee K, Liangruksa M, Termsaithong T, Saparpakorn P, Hannongbua S, Laomettachit T, et al.
ACS Omega . 2023 Oct; 8(41):38373-38385. PMID: 37867669
The mammalian target of rapamycin (mTOR) is a protein kinase of the PI3K/Akt signaling pathway that regulates cell growth and division and is an attractive target for cancer therapy. Many...
9.
Elucidation of benzene sulfonamide derivative binding at a novel interprotomer pocket of wild type and mutants of coxsackievirus B3 viral capsid using molecular dynamics simulations and density functional theory
Prapassornwattana P, Hannongbua S, Saparpakorn P
Biophys Chem . 2023 Sep; 302:107109. PMID: 37748430
Coxsackievirus B3 (CVB3), a serotype of enterovirus B, causes hand, foot, and mouth disease; pericarditis; and myocarditis. A benzene sulfonamide derivative is reported to have inhibitory activity against wild-type (WT)...
10.
Biophysical Characterization of p51 and p66 Monomers of HIV-1 Reverse Transcriptase with Their Inhibitors
Seetaha S, Kamonsutthipaijit N, Yagi-Utsumi M, Seako Y, Yamaguchi T, Hannongbua S, et al.
Protein J . 2023 Sep; 42(6):741-752. PMID: 37728788
Human immunodeficiency virus (HIV)-1 reverse transcriptase (HIV-1 RT) is responsible for the transcription of viral RNA genomes into DNA genomes and has become an important target for the treatment of...