Literature DB >> 16495277

In vitro development of resistance to human immunodeficiency virus protease inhibitor GW640385.

P J Yates1, R Hazen, M St Clair, L Boone, M Tisdale, R C Elston.   

Abstract

Development of in vitro resistance to GW640385, a new human immunodeficiency virus type 1 protease inhibitor, was studied. Variants characterized included one with <4-fold resistance and amino acid substitutions Q58E/A71V (protease) and P452K (Gag) and one with >50-fold resistance and amino acid substitutions L10F/G16E/E21K/A28S/M46I/F53L/A71V (protease) and L449F/P453T (Gag). The A28S substitution substantially reduced replication capacity.

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Year:  2006        PMID: 16495277      PMCID: PMC1426426          DOI: 10.1128/AAC.50.3.1092-1095.2006

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  17 in total

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4.  Amino acid substitutions in Gag protein at non-cleavage sites are indispensable for the development of a high multitude of HIV-1 resistance against protease inhibitors.

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Journal:  J Biol Chem       Date:  2001-12-10       Impact factor: 5.157

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Journal:  J Virol       Date:  2003-04       Impact factor: 5.103

6.  A potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site.

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Journal:  J Virol       Date:  2002-08       Impact factor: 5.103

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  9 in total

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Journal:  J Virol       Date:  2010-09-01       Impact factor: 5.103

4.  A novel HIV-1 protease inhibitor, GRL-044, has potent activity against various HIV-1s with an extremely high genetic barrier to the emergence of HIV-1 drug resistance.

Authors:  Manabu Aoki; Simon B Chang; Debananda Das; Cuthbert Martyr; Nicole S Delino; Yuki Takamatsu; Arun K Ghosh; Hiroaki Mitsuya
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5.  Novel Protease Inhibitors Containing C-5-Modified bis-Tetrahydrofuranylurethane and Aminobenzothiazole as P2 and P2' Ligands That Exert Potent Antiviral Activity against Highly Multidrug-Resistant HIV-1 with a High Genetic Barrier against the Emergence of Drug Resistance.

Authors:  Yuki Takamatsu; Manabu Aoki; Haydar Bulut; Debananda Das; Masayuki Amano; Venkata Reddy Sheri; Ladislau C Kovari; Hironori Hayashi; Nicole S Delino; Arun K Ghosh; Hiroaki Mitsuya
Journal:  Antimicrob Agents Chemother       Date:  2019-07-25       Impact factor: 5.191

6.  Drug-associated changes in amino acid residues in Gag p2, p7(NC), and p6(Gag)/p6(Pol) in human immunodeficiency virus type 1 (HIV-1) display a dominant effect on replicative fitness and drug response.

Authors:  Sarah K Ho; Roxana M Coman; Joshua C Bunger; Stephanie L Rose; Patricia O'Brien; Isabel Munoz; Ben M Dunn; John W Sleasman; Maureen M Goodenow
Journal:  Virology       Date:  2008-07-02       Impact factor: 3.616

7.  In vitro antiviral activity of the novel, tyrosyl-based human immunodeficiency virus (HIV) type 1 protease inhibitor brecanavir (GW640385) in combination with other antiretrovirals and against a panel of protease inhibitor-resistant HIV.

Authors:  Richard Hazen; Robert Harvey; Robert Ferris; Charles Craig; Phillip Yates; Philip Griffin; John Miller; Istvan Kaldor; John Ray; Vincente Samano; Eric Furfine; Andrew Spaltenstein; Michael Hale; Roger Tung; Marty St Clair; Mary Hanlon; Lawrence Boone
Journal:  Antimicrob Agents Chemother       Date:  2007-07-09       Impact factor: 5.191

8.  Added value of deep sequencing relative to population sequencing in heavily pre-treated HIV-1-infected subjects.

Authors:  Francisco M Codoñer; Christian Pou; Alexander Thielen; Federico García; Rafael Delgado; David Dalmau; Miguel Álvarez-Tejado; Lidia Ruiz; Bonaventura Clotet; Roger Paredes
Journal:  PLoS One       Date:  2011-05-13       Impact factor: 3.240

Review 9.  Human Immunodeficiency Virus Gag and protease: partners in resistance.

Authors:  Axel Fun; Annemarie M J Wensing; Jens Verheyen; Monique Nijhuis
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  9 in total

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