Recent advances in natural anti‐HIV triterpenoids and analogs
- 14 July 2020
- journal article
- review article
- Published by Wiley in Medicinal Research Reviews
- Vol. 40 (6) , 2339-2385
Abstract
The human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS) epidemic is one of the world's most serious health challenges. Although combination antiretroviral therapy provides effective viral suppression, current medicines used against HIV cannot completely eradicate the infectious disease and often have associated toxicities and severe side effects in addition to causing drug resistance. Therefore, the continued development of new antiviral agents with diverse structures and novel mechanisms of action remains a vital need for the management of HIV/AIDS. Natural products are an important source of drug discovery, and certain triterpenes and their analogs have demonstrated potential as pharmaceutical precursors for the treatment of HIV. Over the past decade, natural triterpenoids and analogs have been extensively studied to find new anti‐HIV drugs. This review discusses the anti‐HIV triterpenoids and analogs reported during the period of 2009–2019. The article includes not only a comprehensive review of the recent anti‐HIV agent development from the perspective of medicinal chemistry, but also discusses structure–activity relationship analyses of the described triterpenoids.Keywords
Funding Information
- National Institute of Allergy and Infectious Diseases (AI‐033066)
This publication has 114 references indexed in Scilit:
- Protostane and Fusidane Triterpenes: A Mini-ReviewMolecules, 2013
- Anti-AIDS agents 88. Anti-HIV conjugates of betulin and betulinic acid with AZT prepared via click chemistryTetrahedron Letters, 2012
- Celastrol Inhibits Tat-Mediated Human Immunodeficiency Virus (HIV) Transcription and ReplicationJournal of Molecular Biology, 2011
- Efficient synthesis and biological evaluation of epiceanothic acid and related compoundsBioorganic & Medicinal Chemistry Letters, 2011
- Triterpene derivatives that inhibit human immunodeficiency virus type 1 replicationBioorganic & Medicinal Chemistry Letters, 2011
- Conjugates of betulin derivatives with AZT as potent anti-HIV agentsBioorganic & Medicinal Chemistry, 2010
- Anti-AIDS Agents 81. Design, Synthesis, and Structure−Activity Relationship Study of Betulinic Acid and Moronic Acid Derivatives as Potent HIV Maturation InhibitorsJournal of Medicinal Chemistry, 2010
- Discovery and Development of Natural Product-Derived Chemotherapeutic Agents Based on a Medicinal Chemistry ApproachJournal of Natural Products, 2010
- Betulinic Acid Derivatives as Human Immunodeficiency Virus Type 2 (HIV-2) InhibitorsJournal of Medicinal Chemistry, 2009
- Anti-AIDS Agents. 78. Design, Synthesis, Metabolic Stability Assessment, and Antiviral Evaluation of Novel Betulinic Acid Derivatives as Potent Anti-Human Immunodeficiency Virus (HIV) AgentsJournal of Medicinal Chemistry, 2009