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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...

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Autores principales: Li, Xiaoyuan, Li, Yuexiang, Fan, Shiyong, Cao, Ruiyuan, Li, Xiaojia, He, Xiaomeng, Li, Wei, Xu, Longfa, Cheng, Tong, Li, Honglin, Zhong, Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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