Literature DB >> 22095518

HIV-1 integrase inhibitors: a review of their chemical development.

Kundan B Ingale1, Manish S Bhatia.   

Abstract

Highly active antiretroviral therapy (HAART) significantly decreases plasma viral load, increases CD4+ T-cell counts in HIV-1-infected patients and has reduced progression to AIDS in developed countries. However, adverse side effects, and emergence of drug resistance, mean there is still a demand for new anti-HIV agents. The HIV integrase (IN) is a target that has been the focus of rational drug design over the past decade. In 2007, raltegravir was the first IN inhibitor approved by the US Food and Drug Administration for antiretroviral combination therapy, while another IN inhibitor, elvitegravir, is currently in Phase III clinical trials. This article reviews the development and resistance profiling of small molecule HIV-1 IN inhibitors.

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Year:  2011        PMID: 22095518     DOI: 10.3851/IMP1740

Source DB:  PubMed          Journal:  Antivir Chem Chemother        ISSN: 0956-3202


  7 in total

Review 1.  Targeting Metalloenzymes for Therapeutic Intervention.

Authors:  Allie Y Chen; Rebecca N Adamek; Benjamin L Dick; Cy V Credille; Christine N Morrison; Seth M Cohen
Journal:  Chem Rev       Date:  2018-09-07       Impact factor: 60.622

2.  Recombinant rabbit single-chain antibodies bind to the catalytic and C-terminal domains of HIV-1 integrase protein and strongly inhibit HIV-1 replication.

Authors:  Frederico Aires da Silva; Min Li; Sylvie Rato; Sara Maia; Rui Malhó; Kylie Warren; David Harrich; Robert Craigie; Carlos Barbas; Joao Goncalves
Journal:  Biotechnol Appl Biochem       Date:  2012-10-10       Impact factor: 2.431

3.  Evaluation of novel N'-(3-hydroxybenzoyl)-2-oxo-2H-chromene-3-carbohydrazide derivatives as potential HIV-1 integrase inhibitors.

Authors:  Omobolanle J Jesumoroti; Dumisani Mnkandhla; Michelle Isaacs; Heinrich C Hoppe; Rosalyn Klein
Journal:  Medchemcomm       Date:  2018-12-10       Impact factor: 3.597

4.  Development of elvitegravir resistance and linkage of integrase inhibitor mutations with protease and reverse transcriptase resistance mutations.

Authors:  Mark A Winters; Robert M Lloyd; Robert W Shafer; Michael J Kozal; Michael D Miller; Mark Holodniy
Journal:  PLoS One       Date:  2012-07-18       Impact factor: 3.240

5.  Identification of a novel type of small molecule inhibitor against HIV-1.

Authors:  Byung Soo Kim; Jung Ae Park; Min-Jung Kim; Seon Hee Kim; Kyung Lee Yu; Ji Chang You
Journal:  BMB Rep       Date:  2015-02       Impact factor: 4.778

6.  Molecular docking study of lamellarin analogues and identification of potential inhibitors of HIV-1 integrase strand transfer complex by virtual screening.

Authors:  Chatchakorn Eurtivong; Kiattawee Choowongkomon; Poonsakdi Ploypradith; Somsak Ruchirawat
Journal:  Heliyon       Date:  2019-11-14

7.  Quinolines from the cyclocondensation of isatoic anhydride with ethyl acetoacetate: preparation of ethyl 4-hydroxy-2-methylquinoline-3-carboxylate and derivatives.

Authors:  Nicholas G Jentsch; Jared D Hume; Emily B Crull; Samer M Beauti; Amy H Pham; Julie A Pigza; Jacques J Kessl; Matthew G Donahue
Journal:  Beilstein J Org Chem       Date:  2018-09-28       Impact factor: 2.544

  7 in total

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