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In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights
The HIV/AIDS pandemic is a serious threat to the health and development of mankind, which has affected about 37.9 million people worldwide. The increasing negative health, economic and social impacts of this disease have led to the search for new therapeutic candidates for the mitigation of AIDS/HIV...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033207/ https://www.ncbi.nlm.nih.gov/pubmed/35480193 http://dx.doi.org/10.1039/d0ra10655k |
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author | Kumar, Dinesh Sharma, Pooja Shabu, Kaur, Ramandeep Lobe, Maloba M. M. Gupta, Girish K. Ntie-Kang, Fidele |
author_facet | Kumar, Dinesh Sharma, Pooja Shabu, Kaur, Ramandeep Lobe, Maloba M. M. Gupta, Girish K. Ntie-Kang, Fidele |
author_sort | Kumar, Dinesh |
collection | PubMed |
description | The HIV/AIDS pandemic is a serious threat to the health and development of mankind, which has affected about 37.9 million people worldwide. The increasing negative health, economic and social impacts of this disease have led to the search for new therapeutic candidates for the mitigation of AIDS/HIV. However, to date, there is still no treatment that can cure this disease. Furthermore, the clinically available drugs have numerous severe side effects. Hence, the synthesis of novel agents from natural leads is one of the rational approaches to obtain new drugs in modern medicinal chemistry. This review article is an effort to summarize recent developments with regards to the discovery of novel analogs with promising biological potential against HIV/AIDS. Herein, we also aim to discuss prospective directions on the progress of more credible and specific analogues. Besides presenting design strategies, the present communication also highlights the structure–activity relationship together with the structural features of the most promising molecules, their IC(50) values, mechanistic insights and some interesting key findings revealed during their biological evaluation. The interactions with the amino acid residues of the enzymes responsible for HIV-1 inhibition are also discussed. This collection will be of great interest for researchers working in this area. |
format | Online Article Text |
id | pubmed-9033207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90332072022-04-26 In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights Kumar, Dinesh Sharma, Pooja Shabu, Kaur, Ramandeep Lobe, Maloba M. M. Gupta, Girish K. Ntie-Kang, Fidele RSC Adv Chemistry The HIV/AIDS pandemic is a serious threat to the health and development of mankind, which has affected about 37.9 million people worldwide. The increasing negative health, economic and social impacts of this disease have led to the search for new therapeutic candidates for the mitigation of AIDS/HIV. However, to date, there is still no treatment that can cure this disease. Furthermore, the clinically available drugs have numerous severe side effects. Hence, the synthesis of novel agents from natural leads is one of the rational approaches to obtain new drugs in modern medicinal chemistry. This review article is an effort to summarize recent developments with regards to the discovery of novel analogs with promising biological potential against HIV/AIDS. Herein, we also aim to discuss prospective directions on the progress of more credible and specific analogues. Besides presenting design strategies, the present communication also highlights the structure–activity relationship together with the structural features of the most promising molecules, their IC(50) values, mechanistic insights and some interesting key findings revealed during their biological evaluation. The interactions with the amino acid residues of the enzymes responsible for HIV-1 inhibition are also discussed. This collection will be of great interest for researchers working in this area. The Royal Society of Chemistry 2021-05-18 /pmc/articles/PMC9033207/ /pubmed/35480193 http://dx.doi.org/10.1039/d0ra10655k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Kumar, Dinesh Sharma, Pooja Shabu, Kaur, Ramandeep Lobe, Maloba M. M. Gupta, Girish K. Ntie-Kang, Fidele In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
title | In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
title_full | In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
title_fullStr | In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
title_full_unstemmed | In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
title_short | In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
title_sort | in search of therapeutic candidates for hiv/aids: rational approaches, design strategies, structure–activity relationship and mechanistic insights |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033207/ https://www.ncbi.nlm.nih.gov/pubmed/35480193 http://dx.doi.org/10.1039/d0ra10655k |
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