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    TMC310911, a Novel Human Immunodeficiency Virus Type 1 Protease Inhibitor, Shows In Vitro an Improved Resistance Profile and Higher Genetic Barrier to Resistance Compared with Current Protease Inhibitors

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    Authors
    Dierynck, Inge
    Van Marck, Herwig
    Van Ginderen, Marcia
    Jonckers, Tim H. M.
    Nalam, Madhavi N. L.
    Schiffer, Celia A.
    Raoof, Araz
    Kraus, Guenter
    Picchio, Gaston
    UMass Chan Affiliations
    Department of Biochemistry and Molecular Pharmacology
    Document Type
    Journal Article
    Publication Date
    2011-12-08
    Keywords
    Drug Resistance, Viral
    HIV Antigens
    HIV Protease Inhibitors
    HIV-1
    Humans
    Virus Replication
    gag Gene Products, Human Immunodeficiency Virus
    Biochemistry, Biophysics, and Structural Biology
    Microbiology
    
    Metadata
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    Link to Full Text
    http://dx.doi.org/10.1128/AAC.00748-11
    Abstract
    TMC310911 is a novel human immunodeficiency virus type 1 (HIV-1) protease inhibitor (PI) structurally closely related to darunavir (DRV) but with improved virological characteristics. TMC310911 has potent activity against wild-type (WT) HIV-1 (median 50% effective concentration [EC(50)], 14 nM) and a wide spectrum of recombinant HIV-1 clinical isolates, including multiple-PI-resistant strains with decreased susceptibility to currently approved PIs (fold change [FC] in EC(50), >10). For a panel of 2,011 recombinant clinical isolates with decreased susceptibility to at least one of the currently approved PIs, the FC in TMC310911 EC(50) was
    Source
    Antimicrob Agents Chemother. 2011 Dec;55(12):5723-31. Epub 2011 Sep 6. Link to article on publisher's site
    DOI
    10.1128/AAC.00748-11
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/26001
    PubMed ID
    21896904
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1128/AAC.00748-11
    Scopus Count
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    UMass Chan Faculty and Researcher Publications
    Schiffer Lab Publications

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