Loading…
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...
Saved in:
Published in: | Bioorganic & medicinal chemistry 2024-09, Vol.111, p.117860, Article 117860 |
---|---|
Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c235t-59fe2f37cb51f229aba38b1fe1488e1210db5bc445f737c6455516f9a71113dc3 |
container_end_page | |
container_issue | |
container_start_page | 117860 |
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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3087561798</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0968089624002748</els_id><sourcerecordid>3087561798</sourcerecordid><originalsourceid>FETCH-LOGICAL-c235t-59fe2f37cb51f229aba38b1fe1488e1210db5bc445f737c6455516f9a71113dc3</originalsourceid><addsrcrecordid>eNp9kLlOxDAQQC0EguX4ABrkkiaLJ46TWFRoxSUh0QCisxxnDF45B3aCxN9jWKCkmubNG80j5BjYEhiUZ-tl05llzvJiCVDVJdsiCyjKIuNcwjZZMFnWGatluUf2Y1wzlkgJu2SPSyYLkVcL8ryaQ8B-onHS0xzpYOn0ijR22nvaDR7N7JHqfnLZze0TbcP8Eqnrv6HRjehdj3QINKBJFv9B9TiG4R3bQ7JjtY949DMPyOPV5cPqJru7v75dXdxlJudiyoS0mFtemUaAzXOpG83rBixCUdcIObC2EY0pCmGrRJWFEAJKK3UFALw1_ICcbrzp7NuMcVKdiwa91z0Oc1Sc1ZUooZJ1QmGDmjDEGNCqMbhOhw8FTH0FVWuVgqqvoGoTNO2c_OjnpsP2b-O3YALONwCmJ98dBhWNw95g61KTSbWD-0f_CRUEhac</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3087561798</pqid></control><display><type>article</type><title>Current status of the small molecule anti-HIV drugs in the pipeline or recently approved</title><source>ScienceDirect Freedom Collection 2022-2024</source><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</creator><creatorcontrib>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</creatorcontrib><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.</description><identifier>ISSN: 0968-0896</identifier><identifier>ISSN: 1464-3391</identifier><identifier>EISSN: 1464-3391</identifier><identifier>DOI: 10.1016/j.bmc.2024.117860</identifier><identifier>PMID: 39094527</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Anti-HIV drugs ; Drug discovery ; HIV-1 ; HIV-2 ; Mechanism of action</subject><ispartof>Bioorganic & medicinal chemistry, 2024-09, Vol.111, p.117860, Article 117860</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c235t-59fe2f37cb51f229aba38b1fe1488e1210db5bc445f737c6455516f9a71113dc3</cites><orcidid>0000-0002-5684-9607</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39094527$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Umumararungu, Théoneste</creatorcontrib><creatorcontrib>Nyandwi, Jean Baptiste</creatorcontrib><creatorcontrib>Katandula, Jonathan</creatorcontrib><creatorcontrib>Twizeyimana, Eric</creatorcontrib><creatorcontrib>Claude Tomani, Jean</creatorcontrib><creatorcontrib>Gahamanyi, Noël</creatorcontrib><creatorcontrib>Ishimwe, Nestor</creatorcontrib><creatorcontrib>Olawode, Emmanuel Oladayo</creatorcontrib><creatorcontrib>Habarurema, Gratien</creatorcontrib><creatorcontrib>Mpenda, Matabishi</creatorcontrib><creatorcontrib>Uyisenga, Jeanne Primitive</creatorcontrib><creatorcontrib>Saeed, Shamsaldeen Ibrahim</creatorcontrib><title>Current status of the small molecule anti-HIV drugs in the pipeline or recently approved</title><title>Bioorganic & medicinal chemistry</title><addtitle>Bioorg Med Chem</addtitle><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.</description><subject>Anti-HIV drugs</subject><subject>Drug discovery</subject><subject>HIV-1</subject><subject>HIV-2</subject><subject>Mechanism of action</subject><issn>0968-0896</issn><issn>1464-3391</issn><issn>1464-3391</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kLlOxDAQQC0EguX4ABrkkiaLJ46TWFRoxSUh0QCisxxnDF45B3aCxN9jWKCkmubNG80j5BjYEhiUZ-tl05llzvJiCVDVJdsiCyjKIuNcwjZZMFnWGatluUf2Y1wzlkgJu2SPSyYLkVcL8ryaQ8B-onHS0xzpYOn0ijR22nvaDR7N7JHqfnLZze0TbcP8Eqnrv6HRjehdj3QINKBJFv9B9TiG4R3bQ7JjtY949DMPyOPV5cPqJru7v75dXdxlJudiyoS0mFtemUaAzXOpG83rBixCUdcIObC2EY0pCmGrRJWFEAJKK3UFALw1_ICcbrzp7NuMcVKdiwa91z0Oc1Sc1ZUooZJ1QmGDmjDEGNCqMbhOhw8FTH0FVWuVgqqvoGoTNO2c_OjnpsP2b-O3YALONwCmJ98dBhWNw95g61KTSbWD-0f_CRUEhac</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Umumararungu, Théoneste</creator><creator>Nyandwi, Jean Baptiste</creator><creator>Katandula, Jonathan</creator><creator>Twizeyimana, Eric</creator><creator>Claude Tomani, Jean</creator><creator>Gahamanyi, Noël</creator><creator>Ishimwe, Nestor</creator><creator>Olawode, Emmanuel Oladayo</creator><creator>Habarurema, Gratien</creator><creator>Mpenda, Matabishi</creator><creator>Uyisenga, Jeanne Primitive</creator><creator>Saeed, Shamsaldeen Ibrahim</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5684-9607</orcidid></search><sort><creationdate>20240901</creationdate><title>Current status of the small molecule anti-HIV drugs in the pipeline or recently approved</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c235t-59fe2f37cb51f229aba38b1fe1488e1210db5bc445f737c6455516f9a71113dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anti-HIV drugs</topic><topic>Drug discovery</topic><topic>HIV-1</topic><topic>HIV-2</topic><topic>Mechanism of action</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Umumararungu, Théoneste</creatorcontrib><creatorcontrib>Nyandwi, Jean Baptiste</creatorcontrib><creatorcontrib>Katandula, Jonathan</creatorcontrib><creatorcontrib>Twizeyimana, Eric</creatorcontrib><creatorcontrib>Claude Tomani, Jean</creatorcontrib><creatorcontrib>Gahamanyi, Noël</creatorcontrib><creatorcontrib>Ishimwe, Nestor</creatorcontrib><creatorcontrib>Olawode, Emmanuel Oladayo</creatorcontrib><creatorcontrib>Habarurema, Gratien</creatorcontrib><creatorcontrib>Mpenda, Matabishi</creatorcontrib><creatorcontrib>Uyisenga, Jeanne Primitive</creatorcontrib><creatorcontrib>Saeed, Shamsaldeen Ibrahim</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic & medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Umumararungu, Théoneste</au><au>Nyandwi, Jean Baptiste</au><au>Katandula, Jonathan</au><au>Twizeyimana, Eric</au><au>Claude Tomani, Jean</au><au>Gahamanyi, Noël</au><au>Ishimwe, Nestor</au><au>Olawode, Emmanuel Oladayo</au><au>Habarurema, Gratien</au><au>Mpenda, Matabishi</au><au>Uyisenga, Jeanne Primitive</au><au>Saeed, Shamsaldeen Ibrahim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current status of the small molecule anti-HIV drugs in the pipeline or recently approved</atitle><jtitle>Bioorganic & medicinal chemistry</jtitle><addtitle>Bioorg Med Chem</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>111</volume><spage>117860</spage><pages>117860-</pages><artnum>117860</artnum><issn>0968-0896</issn><issn>1464-3391</issn><eissn>1464-3391</eissn><abstract>[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.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39094527</pmid><doi>10.1016/j.bmc.2024.117860</doi><orcidid>https://orcid.org/0000-0002-5684-9607</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0968-0896 |
ispartof | Bioorganic & medicinal chemistry, 2024-09, Vol.111, p.117860, Article 117860 |
issn | 0968-0896 1464-3391 1464-3391 |
language | eng |
recordid | cdi_proquest_miscellaneous_3087561798 |
source | ScienceDirect Freedom Collection 2022-2024 |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-31T23%3A48%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Current%20status%20of%20the%20small%20molecule%20anti-HIV%20drugs%20in%20the%20pipeline%20or%20recently%20approved&rft.jtitle=Bioorganic%20&%20medicinal%20chemistry&rft.au=Umumararungu,%20Th%C3%A9oneste&rft.date=2024-09-01&rft.volume=111&rft.spage=117860&rft.pages=117860-&rft.artnum=117860&rft.issn=0968-0896&rft.eissn=1464-3391&rft_id=info:doi/10.1016/j.bmc.2024.117860&rft_dat=%3Cproquest_cross%3E3087561798%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c235t-59fe2f37cb51f229aba38b1fe1488e1210db5bc445f737c6455516f9a71113dc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3087561798&rft_id=info:pmid/39094527&rfr_iscdi=true |