Inhibition of hepatitis B virus replication by N -hydroxyisoquinolinediones and related polyoxygenated heterocycles-Reference-Cited by-同舟云学术

Inhibition of hepatitis B virus replication by N -hydroxyisoquinolinediones and related polyoxygenated heterocycles

Published:2017-07 Issue: Volume:143 Page:205-217
ISSN:0166-3542
Container-title:Antiviral Research
language:en
Short-container-title:Antiviral Research

Author:

Edwards Tiffany C.,Lomonosova Elena,Patel Jenny A.,Li Qilan,Villa Juan A.,Gupta Ankit K.,Morrison Lynda A.^ORCID,Bailly Fabrice,Cotelle Philippe,Giannakopoulou Erofili,Zoidis Grigoris^ORCID,Tavis John E.

Funder

JET

Saint Louis University Cancer Center

Ministère de l’Enseignement Supérieur et de la Recherche Française

l’Agence Nationale de la Recherche contre le Sida

Publisher

Elsevier BV

Subject

Virology,Pharmacology

Reference44 articles.

1. Design, synthesis, and biological evaluation of a series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as dual inhibitors of human immunodeficiency virus type 1 integrase and the reverse transcriptase RNase H domain;Billamboz;J. Med. Chem.,2008

2. 2-hydroxyisoquinoline-1,3(2H,4H)-diones as inhibitors of HIV-1 integrase and reverse transcriptase RNase H domain: influence of the alkylation of position 4;Billamboz;Eur. J. Med. Chem.,2011

3. Magnesium chelating 2-hydroxyisoquinoline-1,3(2H,4H)-diones, as inhibitors of HIV-1 integrase and/or the HIV-1 reverse transcriptase ribonuclease H domain: discovery of a novel selective inhibitor of the ribonuclease H function;Billamboz;J. Med. Chem.,2011

4. 2-hydroxyisoquinoline-1, 3 (2H, 4H)-diones (HIDs) as human immunodeficiency virus type 1 integrase inhibitors: influence of the alkylcarboxamide substitution of position 4;Billamboz;Eur. J. Med. Chem.,2016

5. 4-Substituted 2-hydroxyisoquinoline-1,3(2H,4H)-diones, as a novel class of HIV-1 integrase inhibitors;Billamboz;Acs. Med. Chem. Lett.,2013

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