Synthetic Approaches to a Key Pyridone-carboxylic Acid Precursor Common to the HIV-1 Integrase Strand Transfer Inhibitors Dolutegravir, Bictegravir, and Cabotegravir
Author:
Affiliation:
1. Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States
Funder
National Cancer Institute
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.3c00063
Reference28 articles.
1. HIV Fact Sheet. World Health Organization, November 9, 2022. https://www.who.int/news-room/fact-sheets/detail/hiv-aids (accessed 2023-02-14).
2. Human Immunodeficiency Virus/AIDS in the Era of Coronavirus Disease 2019: A Juxtaposition of 2 Pandemics
3. Update and latest advances in antiretroviral therapy
4. New designs for HIV-1 integrase inhibitors: a patent review (2018-present)
5. Retroviral DNA Integration
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1. Carbamoyl 1,4-Dihydropyridine Derivatives: Synthesis and Impressive Antidiabetic Activity;Russian Journal of Organic Chemistry;2024-05
2. N-Substituted Bicyclic Carbamoyl Pyridones: Integrase Strand Transfer Inhibitors that Potently Inhibit Drug-Resistant HIV-1 Integrase Mutants;ACS Infectious Diseases;2024-02-12
3. Synthetic approaches and application of clinically approved small-molecule Anti-HIV drugs: An update;European Journal of Medicinal Chemistry;2023-12
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