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Anh-Tien Ton
Anh-Tien Ton
University of British Columbia
Verified email at prostatecentre.com
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Cited by
Year
Rapid identification of potential inhibitors of SARS‐CoV‐2 main protease by deep docking of 1.3 billion compounds
AT Ton, F Gentile, M Hsing, F Ban, A Cherkasov
Molecular informatics 39 (8), 2000028, 2020
5012020
Deep docking: a deep learning platform for augmentation of structure based drug discovery
F Gentile, V Agrawal, M Hsing, AT Ton, F Ban, U Norinder, ME Gleave, ...
ACS central science 6 (6), 939-949, 2020
255*2020
Crystallographic structure of wild-type SARS-CoV-2 main protease acyl-enzyme intermediate with physiological C-terminal autoprocessing site
J Lee, LJ Worrall, M Vuckovic, FI Rosell, F Gentile, AT Ton, NA Caveney, ...
Nature communications 11 (1), 5877, 2020
1622020
Artificial intelligence–enabled virtual screening of ultra-large chemical libraries with deep docking
F Gentile, JC Yaacoub, J Gleave, M Fernandez, AT Ton, F Ban, A Stern, ...
Nature Protocols 17 (3), 672-697, 2022
1562022
Automated discovery of noncovalent inhibitors of SARS-CoV-2 main protease by consensus Deep Docking of 40 billion small molecules
F Gentile, M Fernandez, F Ban, AT Ton, H Mslati, CF Perez, E Leblanc, ...
Chemical science 12 (48), 15960-15974, 2021
472021
X-ray crystallographic characterization of the SARS-CoV-2 main protease polyprotein cleavage sites essential for viral processing and maturation
J Lee, C Kenward, LJ Worrall, M Vuckovic, F Gentile, AT Ton, M Ng, ...
Nature Communications 13 (1), 5196, 2022
402022
Drugging the ‘undruggable’. therapeutic targeting of protein–DNA interactions with the use of computer-aided drug discovery methods
M Radaeva, AT Ton, M Hsing, F Ban, A Cherkasov
Drug Discovery Today, 2021
292021
Targeting SARS-CoV-2 papain-like protease in the postvaccine era
AT Ton, M Pandey, JR Smith, F Ban, M Fernandez, A Cherkasov
Trends in Pharmacological Sciences 43 (11), 906-919, 2022
282022
Molecular basis of interactions between SH3 domain-containing proteins and the proline-rich region of the ubiquitin ligase Itch
G Desrochers, L Cappadocia, M Lussier-Price, AT Ton, R Ayoubi, ...
Journal of Biological Chemistry 292 (15), 6325-6338, 2017
212017
Dual-inhibitors of N-Myc and AURKA as potential therapy for neuroendocrine prostate cancer
AT Ton, K Singh, H Morin, F Ban, E Leblanc, J Lee, N Lallous, ...
International journal of molecular sciences 21 (21), 8277, 2020
192020
A functional substitution in the L‐aromatic amino acid decarboxylase enzyme worsens somatic symptoms via a serotonergic pathway
S Khoury, MH Piltonen, AT Ton, T Cole, A Samoshkin, SB Smith, I Belfer, ...
Annals of neurology 86 (2), 168-180, 2019
122019
Development of VPC-70619, a small-molecule N-Myc inhibitor as a potential therapy for neuroendocrine prostate cancer
AT Ton, J Foo, K Singh, J Lee, A Kalyta, H Morin, C Perez, F Ban, ...
International Journal of Molecular Sciences 23 (5), 2588, 2022
102022
Large-scale virtual screening for the discovery of SARS-CoV-2 papain-like protease (PLpro) non-covalent inhibitors
O Garland, AT Ton, S Moradi, JR Smith, S Kovacic, K Ng, M Pandey, ...
Journal of Chemical Information and Modeling 63 (7), 2158-2169, 2023
82023
A novel class of broad-spectrum active-site-directed 3C-like protease inhibitors with nanomolar antiviral activity against highly immune-evasive SARS-CoV-2 Omicron subvariants
J Pérez-Vargas, LJ Worrall, AD Olmstead, AT Ton, J Lee, I Villanueva, ...
Emerging microbes & infections 12 (2), 2246594, 2023
62023
Myc-max inhibitor compound therapeutics for cancer treatment, methods and uses associated therewith
A Tcherkassov, PS Rennie, F Ban, EJJ Leblanc, LA Carabet, N Lallous, ...
US Patent App. 17/250,810, 2022
12022
Inferring the selection window in antimicrobial resistance using deep mutational scanning data and biophysics-based fitness models
P Dasmeh, AT Ton, C Quach, AWR Serohijos
Biorxiv, 189019, 2017
12017
Structure-based development of a novel MYC inhibitor for neuroendocrine prostate cancer
J Foo, AT Ton, K Singh, F Ban, H Morin, J Lee, E LeBlanc, N Lallous, ...
Cancer Research 82 (12_Supplement), 5731-5731, 2022
2022
Development and application of consensus hit-calling protocols for the virtual screening of ‘undruggable’and difficult drug targets
AT Ton
University of British Columbia, 2022
2022
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