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Current status of the small molecule anti-HIV drugs in the pipeline or recently approved

[Display omitted] Human Immunodeficiency Virus (HIV) is the causative agent of Acquired Immunodeficiency Syndrome (AIDS) with high morbidity and mortality rates. Treatment of AIDS/HIV is being complicated by increasing resistance to currently used antiretroviral (ARV) drugs, mainly in low- and middl...

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Published in:Bioorganic & medicinal chemistry 2024-09, Vol.111, p.117860, Article 117860
Main Authors: Umumararungu, Théoneste, Nyandwi, Jean Baptiste, Katandula, Jonathan, Twizeyimana, Eric, Claude Tomani, Jean, Gahamanyi, Noël, Ishimwe, Nestor, Olawode, Emmanuel Oladayo, Habarurema, Gratien, Mpenda, Matabishi, Uyisenga, Jeanne Primitive, Saeed, Shamsaldeen Ibrahim
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container_title Bioorganic & medicinal chemistry
container_volume 111
creator Umumararungu, Théoneste
Nyandwi, Jean Baptiste
Katandula, Jonathan
Twizeyimana, Eric
Claude Tomani, Jean
Gahamanyi, Noël
Ishimwe, Nestor
Olawode, Emmanuel Oladayo
Habarurema, Gratien
Mpenda, Matabishi
Uyisenga, Jeanne Primitive
Saeed, Shamsaldeen Ibrahim
description [Display omitted] Human Immunodeficiency Virus (HIV) is the causative agent of Acquired Immunodeficiency Syndrome (AIDS) with high morbidity and mortality rates. Treatment of AIDS/HIV is being complicated by increasing resistance to currently used antiretroviral (ARV) drugs, mainly in low- and middle-income countries (LMICs) due to drug misuse, poor drug supply and poor treatment monitoring. However, progress has been made in the development of new ARV drugs, targeting different HIV components (Fig. 1). This review aims at presenting and discussing the progress made towards the discovery of new ARVs that are at different stages of clinical trials as of July 2024. For each compound, the mechanism of action, target biomolecule, genes associated with resistance, efficacy and safety, class, and phase of clinical trial are discussed. These compounds include analogues of nucleoside reverse transcriptase inhibitors (NRTIs) – islatravir and censavudine; non-nucleoside reverse transcriptase inhibitors (NNRTIs) – Rilpivirine, elsulfavirine and doravirine; integrase inhibitors namely cabotegravir and dolutegravir and chemokine coreceptors 5 and 2 (CC5/CCR2) antagonists for example cenicriviroc. Also, fostemsavir is being developed as an attachment inhibitor while lenacapavir, VH4004280 and VH4011499 are capsid inhibitors. Others are maturation inhibitors such as GSK-254, GSK3532795, GSK3739937, GSK2838232, and other compounds labelled as miscellaneous (do not belong to the classical groups of anti-HIV drugs or to the newer classes) such as obefazimod and BIT225. There is a considerable progress in the development of new anti-HIV drugs and the effort will continue since HIV infections has no cure or vaccine till now. Efforts are needed to reduce the toxicity of available drugs or discover new drugs with new classes which can delay the development of resistance.
doi_str_mv 10.1016/j.bmc.2024.117860
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Treatment of AIDS/HIV is being complicated by increasing resistance to currently used antiretroviral (ARV) drugs, mainly in low- and middle-income countries (LMICs) due to drug misuse, poor drug supply and poor treatment monitoring. However, progress has been made in the development of new ARV drugs, targeting different HIV components (Fig. 1). This review aims at presenting and discussing the progress made towards the discovery of new ARVs that are at different stages of clinical trials as of July 2024. For each compound, the mechanism of action, target biomolecule, genes associated with resistance, efficacy and safety, class, and phase of clinical trial are discussed. 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1464-3391
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subjects Anti-HIV drugs
Drug discovery
HIV-1
HIV-2
Mechanism of action
title Current status of the small molecule anti-HIV drugs in the pipeline or recently approved
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