2,3,4-Trihydroxybenzyl-hydrazide analogues as novel potent coxsackievirus B3 3C protease inhibitors-Reference-Cited by-同舟云学术

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2,3,4-Trihydroxybenzyl-hydrazide analogues as novel potent coxsackievirus B3 3C protease inhibitors

Published:2016-09 Issue: Volume:120 Page:202-216
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Kim Bo-Kyoung,Ko Hyojin,Jeon Eun-Seok,Ju Eun-Seon,Jeong Lak Shin,Kim Yong-Chul

Funder

National Research Foundation of South Korea

Ministry of Education, Science and Technology

National Research Foundation (NRF) of Korea

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference28 articles.

1. Inhibition of coxsackievirus B3 in cell cultures and in mice by peptide-conjugated morpholino oligomers targeting the internal ribosome entry site;Yuan;J. Virol.,2006

2. Development of anti-coxsackievirus agents targeting 3C protease;Kim;Bioorg. Med. Chem. Lett.,2012

3. Coxsackievirus B3 VLPs purified by ion exchange chromatography elicit strong immune responses in mice;Koho;Antivir. Res.,2014

4. Structural basis of inhibition specificities of 3C and 3C-like proteases by zinc-coordinating and peptidomimetic compounds;Lee;J. Biol. Chem.,2009

5. Virus-receptor interactions of coxsackie B viruses and their putative influence on cardiotropism;Selinka;Med. Microbiol. Immunol.,2004

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