In silico repurposed drugs against monkeypox virus

Monkeypox is an emerging epidemic of concern. The disease is caused by the monkeypox virus and an increasing global incidence with a 2022 outbreak that has spread to Europe amid the COVID-19 pandemic. The new outbreak is associated with novel, previously undiscovered mutations and variants. Currentl...

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Main Authors: Lam, Hilbert Yuen In, Guan, Jia Sheng, Mu, Yuguang
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/167020
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1670202023-05-15T15:33:07Z In silico repurposed drugs against monkeypox virus Lam, Hilbert Yuen In Guan, Jia Sheng Mu, Yuguang School of Biological Sciences Skin Research Lab, A*STAR Science::Biological sciences In Silico Monkeypox Monkeypox is an emerging epidemic of concern. The disease is caused by the monkeypox virus and an increasing global incidence with a 2022 outbreak that has spread to Europe amid the COVID-19 pandemic. The new outbreak is associated with novel, previously undiscovered mutations and variants. Currently, the US Food and Drug Administration (FDA) approved poxvirus treatment involves the use of tecovirimat. However, there is otherwise limited pharmacopoeia and research interest in monkeypox. In this study, virtual screening and molecular dynamics were employed to explore the potential repurposing of multiple drugs previously approved by the FDA or other jurisdictions for other applications. Several drugs are predicted to tightly bind to viral proteins, which are crucial in viral replication, including molecules which show high potential for binding the monkeypox D13L capsid protein, whose inhibition has previously been demonstrated to suppress viral replication. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Skin Research Institute of Singapore (SRIS) Published version This work is supported by the Singapore Ministry of Education (MOE) Tier 1 grant RG27/21 and Tier 2 grant MOE-T2EP30120-0007. Thomas Larry Dawson and Hilbert Lam Yuen In weresupported by funding from the Agency for Science, Technology and Research (A*STAR) and A*STARBMRC EDB IAF-PP grants (H17/01/a0/004, Skin Research Institute of Singapore, and H18/01a0/016,Asian Skin Microbiome Program). 2023-05-10T01:20:21Z 2023-05-10T01:20:21Z 2022 Journal Article Lam, H. Y. I., Guan, J. S. & Mu, Y. (2022). In silico repurposed drugs against monkeypox virus. Molecules, 27(16), 5277-. https://dx.doi.org/10.3390/molecules27165277 1420-3049 https://hdl.handle.net/10356/167020 10.3390/molecules27165277 36014515 2-s2.0-85136545165 16 27 5277 en RG27/21 MOE-T2EP30120-0007 H17/01/a0/004 H18/01a0/016 Molecules © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
In Silico
Monkeypox
spellingShingle Science::Biological sciences
In Silico
Monkeypox
Lam, Hilbert Yuen In
Guan, Jia Sheng
Mu, Yuguang
In silico repurposed drugs against monkeypox virus
description Monkeypox is an emerging epidemic of concern. The disease is caused by the monkeypox virus and an increasing global incidence with a 2022 outbreak that has spread to Europe amid the COVID-19 pandemic. The new outbreak is associated with novel, previously undiscovered mutations and variants. Currently, the US Food and Drug Administration (FDA) approved poxvirus treatment involves the use of tecovirimat. However, there is otherwise limited pharmacopoeia and research interest in monkeypox. In this study, virtual screening and molecular dynamics were employed to explore the potential repurposing of multiple drugs previously approved by the FDA or other jurisdictions for other applications. Several drugs are predicted to tightly bind to viral proteins, which are crucial in viral replication, including molecules which show high potential for binding the monkeypox D13L capsid protein, whose inhibition has previously been demonstrated to suppress viral replication.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Lam, Hilbert Yuen In
Guan, Jia Sheng
Mu, Yuguang
format Article
author Lam, Hilbert Yuen In
Guan, Jia Sheng
Mu, Yuguang
author_sort Lam, Hilbert Yuen In
title In silico repurposed drugs against monkeypox virus
title_short In silico repurposed drugs against monkeypox virus
title_full In silico repurposed drugs against monkeypox virus
title_fullStr In silico repurposed drugs against monkeypox virus
title_full_unstemmed In silico repurposed drugs against monkeypox virus
title_sort in silico repurposed drugs against monkeypox virus
publishDate 2023
url https://hdl.handle.net/10356/167020
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