Aryl diketoacids (ADK) selectively inhibit duplex DNA-unwinding activity of SARS coronavirus NTPase/helicase-Reference-Cited by-同舟云学术

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Aryl diketoacids (ADK) selectively inhibit duplex DNA-unwinding activity of SARS coronavirus NTPase/helicase

Published:2009-03 Issue:6 Volume:19 Page:1636-1638
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Lee Chaewoon,Lee Jin Moo,Lee Na-Ra,Jin Bong-Suk,Jang Kyoung Jin,Kim Dong-Eun,Jeong Yong-Joo,Chong Youhoon

Publisher

Elsevier BV

Subject

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

Reference17 articles.

1. Herpes simplex virus helicase-primase inhibitors are active in animal models of human disease

2. Nucleotide triphosphatase/helicase of hepatitis C virus as a target for antiviral therapy

3. The Adamantane-Derived Bananins Are Potent Inhibitors of the Helicase Activities and Replication of SARS Coronavirus

4. Tertiary structure prediction of SARS coronavirus helicase

5. The Severe Acute Respiratory Syndrome (SARS) Coronavirus NTPase/Helicase Belongs to a Distinct Class of 5′ to 3′ Viral Helicases

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2. Variable Inhibition of DNA Unwinding Rates Catalyzed by the SARS-CoV-2 Helicase Nsp13 by Structurally Distinct Single DNA Lesions;International Journal of Molecular Sciences;2024-07-19

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4. Diketo acid inhibitors of nsp13 of SARS-CoV-2 block viral replication;Antiviral Research;2023-09

5. Coronaviruses SARS-CoV, MERS-CoV, and SARS-CoV-2 helicase inhibitors: a systematic review of in vitro studies;Journal of Virus Eradication;2023-06

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