Synthesis, structure–activity relationship and in vitro biological evaluation of N-arylethyl isoquinoline derivatives as Coxsackievirus B3 inhibitors-Reference-Cited by-同舟云学术

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Synthesis, structure–activity relationship and in vitro biological evaluation of N-arylethyl isoquinoline derivatives as Coxsackievirus B3 inhibitors

Published:2011-10 Issue:19 Volume:21 Page:5787-5790
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Wang Yan-Xiang,Li Yu-Huan,Li Ying-Hong,Gao Rong-Mei,Wang Hui-Qiang,Liu Yan-Xin,Gao Li-Mei,Lu Qiao-Ni,Jiang Jian-Dong,Song Dan-Qing

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference20 articles.

1. Molecular epidemiology and evolution of coxsackievirus A9

2. The group B coxsackieviruses and myocarditis

3. Treatment of picornavirus infections

4. Myocarditis and dilated cardiomyopathy An inflammatory link

5. The Impact of CVB3 Infection on Host Cell Biology

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3. Antiviral spirooliganones C and D with a unique spiro[bicyclo[2.2.2]octane-2,2′-bicyclo[3.1.0]hexane] carbon skeleton from the roots of Illicium oligandrum;Chinese Chemical Letters;2022-09

4. Prenylated C6–C3 derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity;Phytochemistry;2021-12

5. Library construction of stereochemically diverse isomers of spirooliganin: their total synthesis and antiviral activity;Chemical Science;2021

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