<i>N</i>-Substituted Bicyclic Carbamoyl Pyridones: Integrase Strand Transfer Inhibitors that Potently Inhibit Drug-Resistant HIV-1 Integrase Mutants-Reference-Cited by-同舟云学术

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N-Substituted Bicyclic Carbamoyl Pyridones: Integrase Strand Transfer Inhibitors that Potently Inhibit Drug-Resistant HIV-1 Integrase Mutants

Published:2024-02-12 Issue:3 Volume:10 Page:917-927
ISSN:2373-8227
Container-title:ACS Infectious Diseases
language:en
Short-container-title:ACS Infect. Dis.

Author:

Mahajan Pankaj S.¹^ORCID,Smith Steven J.¹,Li Min²,Craigie Robert²,Hughes Stephen H.³^ORCID,Zhao Xue Zhi¹,Burke Terrence R.¹^ORCID

Affiliation:

1. Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States

2. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, United States

3. HIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States

Funder

National Cancer Institute

National Institute of Diabetes and Digestive and Kidney Diseases

National Institutes of Health, Intramural AIDS Targeted Antiviral Program

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acsinfecdis.3c00525

Reference69 articles.

1. Retroviral DNA Integration

2. Integrase inhibitors to treat HIV/Aids

3. Integrase Strand Transfer Inhibitors Are Effective Anti-HIV Drugs

4. A platform for designing HIV integrase inhibitors. Part 2: A two-metal binding model as a potential mechanism of HIV integrase inhibitors

5. Advances in two-metal chelation inhibitors of HIV integrase

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