TY - JOUR
T1 - Discovery and Optimization of Quinoline Analogues as Novel Potent Antivirals against Enterovirus D68
AU - Li, Xiaoyuan
AU - Li, Yuexiang
AU - Fan, Shiyong
AU - Cao, Ruiyuan
AU - Li, Xiaojia
AU - He, Xiaomeng
AU - Li, Wei
AU - Xu, Longfa
AU - Cheng, Tong
AU - Li, Honglin
AU - Zhong, Wu
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/11/10
Y1 - 2022/11/10
N2 - 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 EC50value 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 (Clint= 10.8 mL/min/kg, t1/2= 148 min) indicated that compound 19 with a novel scaffold was worth further investigation.
AB - 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 EC50value 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 (Clint= 10.8 mL/min/kg, t1/2= 148 min) indicated that compound 19 with a novel scaffold was worth further investigation.
UR - https://www.scopus.com/pages/publications/85140313474
U2 - 10.1021/acs.jmedchem.2c01311
DO - 10.1021/acs.jmedchem.2c01311
M3 - 文章
C2 - 36254462
AN - SCOPUS:85140313474
SN - 0022-2623
VL - 65
SP - 14792
EP - 14808
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 21
ER -