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Recent Developments in the Synthesis of HIV-1 Integrase Strand Transfer Inhibitors Incorporating Pyridine Moiety Review

Journal International Journal of Molecular Sciences
ISSN: 1661-6596 , E-ISSN: 1422-0067
Output data Year: 2023, Volume: 24, Number: 11, Article number : 9314, Pages count : DOI: 10.3390/ijms24119314
Authors Starosotnikov Alexey M. 1 , Bastrakov Maxim A. 1
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry RAS, Leninsky Prosp. 47, 119991 Moscow, Russia

Abstract: Human immunodeficiency virus (HIV) causes one of the most dangerous diseases—acquired immunodeficiency syndrome (AIDS). An estimated about 40 million people are currently living with HIV worldwide, most of whom are already on antiretroviral therapy. This makes the development of effective drugs to combat this virus very relevant. Currently, one of the dynamically developing areas of organic and medicinal chemistry is the synthesis and identification of new compounds capable of inhibiting HIV-1 integrase—one of the HIV enzymes. A significant number of studies on this topic are published annually. Many compounds inhibiting integrase incorporate pyridine core. Therefore, this review is an analysis of the literature on the methods for the synthesis of pyridine-containing HIV-1 integrase inhibitors since 2003 to the present.
Cite: Starosotnikov A.M. , Bastrakov M.A.
Recent Developments in the Synthesis of HIV-1 Integrase Strand Transfer Inhibitors Incorporating Pyridine Moiety
International Journal of Molecular Sciences. 2023. V.24. N11. 9314 . DOI: 10.3390/ijms24119314 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:001005642100001
Scopus: 2-s2.0-85161472526
OpenAlex: W4378574306
Citing:
DB Citing
OpenAlex 12
Web of science 13
Scopus 12
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