Title
Natural products and synthetic analogues against HIV: A perspective to develop new potential anti-HIV drugs
Date Issued
05 April 2022
Access level
metadata only access
Resource Type
review
Author(s)
Popović-Djordjević J.
Giordo R.
Kostić A.
Katanić Stanković J.S.
Tsouh Fokou P.V.
Carbone K.
Martorell M.
Kumar M.
Pintus G.
Sharifi-Rad J.
Docea A.O.
Calina D.
Universidad Arturo Prat
Publisher(s)
Elsevier Masson s.r.l.
Abstract
The human immunodeficiency virus (HIV) is responsible for acquired immune deficiency syndrome (AIDS), one of the major pandemic diseases. Highly active antiretroviral therapy (HAART) is the standard HIV-treatment regimen that usually comprises a combination of three or more antiretroviral drugs. HIV reverse transcriptase inhibitors are the main HAART target, which involves the use of both nucleoside reverse transcriptase inhibitors (NRTIs) and non-nucleoside reverse transcriptase inhibitors (NNRTIs). However, compounds affecting other aspects of HIV replication, such as virus entry and fusion or important viral enzymes, such as integrases and proteases, have also been developed. Natural compounds from different sources, like plants, microbial and marine organisms, showed promising anti-HIV activities to the point of establishing the basis for developing new drugs. Indeed, natural compounds-based therapies have the potential to become more efficient than conventional HAART, with less or no side effects. This review aims to gather and discuss the current information about the anti-HIV activity of natural and synthetic compounds, their history and mechanism of action as well as the role of plants and their bioactive compounds as a source of new anti-HIV drugs.
Volume
233
Language
English
OCDE Knowledge area
Inmunología
Farmacología, Farmacia
Subjects
Scopus EID
2-s2.0-85125775750
PubMed ID
Source
European Journal of Medicinal Chemistry
ISSN of the container
02235234
Sponsor(s)
JPDj and AK acknowledge the Ministry of Education , Science, and Technological development of the Republic of Serbia for the support in the realization of this work (registration number contract: 451-03-68/2022-14/200116 ). JKS appreciates the support of the Ministry of Education, Science and Technological Development of the Republic of Serbia (Agreement No. 451-03-68/2022-14/200378 ). This work was also supported by [ CONICYT PIA/APOYO CCTE AFB170007 ], [Seed #2001050151 and Collaborative #2101050160 – University of Sharjah ] and [Fondo di Ateneo per la Ricerca 2020, University of Sassari ].
Sources of information:
Directorio de Producción Científica
Scopus