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Discovery and Optimization of Quinoline Analogues as Novel Potent Antivirals against Enterovirus D68
[Image: see text] Enterovirus D68 (EV-D68) is a nonpolio enterovirus that is mainly transmitted through respiratory routes and poses a potential threat for large-scale spread. EV-D68 infections mostly cause moderate to severe respiratory diseases in children and potentially induce neurological disea...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661475/ https://www.ncbi.nlm.nih.gov/pubmed/36254462 http://dx.doi.org/10.1021/acs.jmedchem.2c01311 |
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author | Li, Xiaoyuan Li, Yuexiang Fan, Shiyong Cao, Ruiyuan Li, Xiaojia He, Xiaomeng Li, Wei Xu, Longfa Cheng, Tong Li, Honglin Zhong, Wu |
author_facet | Li, Xiaoyuan Li, Yuexiang Fan, Shiyong Cao, Ruiyuan Li, Xiaojia He, Xiaomeng Li, Wei Xu, Longfa Cheng, Tong Li, Honglin Zhong, Wu |
author_sort | Li, Xiaoyuan |
collection | PubMed |
description | [Image: see text] Enterovirus D68 (EV-D68) is a nonpolio enterovirus that is mainly transmitted through respiratory routes and poses a potential threat for large-scale spread. EV-D68 infections mostly cause moderate to severe respiratory diseases in children and potentially induce neurological diseases. However, there are no specific antiviral drugs or vaccines against EV-D68. Herein, through virtual screening and rational design, a series of novel quinoline analogues as anti-EV-D68 agents targeting VP1 were identified. Particularly, 19 exhibited potent antiviral activity with an EC(50) value ranging from 0.05 to 0.10 μM against various EV-D68 strains and showed inhibition of viral replication verified by Western blot, immunofluorescence, and plaque formation assay. Mechanistic studies indicated that the anti-EV-D68 agents work mainly by interacting with VP1. The acceptable bioavailability of 23.9% in rats and significant metabolic stability in human liver microsome (Cl(int) = 10.8 mL/min/kg, t(1/2) = 148 min) indicated that compound 19 with a novel scaffold was worth further investigation. |
format | Online Article Text |
id | pubmed-9661475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96614752022-11-15 Discovery and Optimization of Quinoline Analogues as Novel Potent Antivirals against Enterovirus D68 Li, Xiaoyuan Li, Yuexiang Fan, Shiyong Cao, Ruiyuan Li, Xiaojia He, Xiaomeng Li, Wei Xu, Longfa Cheng, Tong Li, Honglin Zhong, Wu J Med Chem [Image: see text] Enterovirus D68 (EV-D68) is a nonpolio enterovirus that is mainly transmitted through respiratory routes and poses a potential threat for large-scale spread. EV-D68 infections mostly cause moderate to severe respiratory diseases in children and potentially induce neurological diseases. However, there are no specific antiviral drugs or vaccines against EV-D68. Herein, through virtual screening and rational design, a series of novel quinoline analogues as anti-EV-D68 agents targeting VP1 were identified. Particularly, 19 exhibited potent antiviral activity with an EC(50) value ranging from 0.05 to 0.10 μM against various EV-D68 strains and showed inhibition of viral replication verified by Western blot, immunofluorescence, and plaque formation assay. Mechanistic studies indicated that the anti-EV-D68 agents work mainly by interacting with VP1. The acceptable bioavailability of 23.9% in rats and significant metabolic stability in human liver microsome (Cl(int) = 10.8 mL/min/kg, t(1/2) = 148 min) indicated that compound 19 with a novel scaffold was worth further investigation. American Chemical Society 2022-10-18 2022-11-10 /pmc/articles/PMC9661475/ /pubmed/36254462 http://dx.doi.org/10.1021/acs.jmedchem.2c01311 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Li, Xiaoyuan Li, Yuexiang Fan, Shiyong Cao, Ruiyuan Li, Xiaojia He, Xiaomeng Li, Wei Xu, Longfa Cheng, Tong Li, Honglin Zhong, Wu Discovery and Optimization of Quinoline Analogues as Novel Potent Antivirals against Enterovirus D68 |
title | Discovery and
Optimization
of Quinoline Analogues
as Novel Potent Antivirals against Enterovirus D68 |
title_full | Discovery and
Optimization
of Quinoline Analogues
as Novel Potent Antivirals against Enterovirus D68 |
title_fullStr | Discovery and
Optimization
of Quinoline Analogues
as Novel Potent Antivirals against Enterovirus D68 |
title_full_unstemmed | Discovery and
Optimization
of Quinoline Analogues
as Novel Potent Antivirals against Enterovirus D68 |
title_short | Discovery and
Optimization
of Quinoline Analogues
as Novel Potent Antivirals against Enterovirus D68 |
title_sort | discovery and
optimization
of quinoline analogues
as novel potent antivirals against enterovirus d68 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661475/ https://www.ncbi.nlm.nih.gov/pubmed/36254462 http://dx.doi.org/10.1021/acs.jmedchem.2c01311 |
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