Phase I and II study of the safety, virologic effect, and pharmacokinetics/pharmacodynamics of single-dose 3-o-(3',3'-dimethylsuccinyl)betulinic acid (bevirimat) against human immunodeficiency virus infection
about
Potent activity of the HIV-1 maturation inhibitor bevirimat in SCID-hu Thy/Liv miceIn vitro selection of clinically relevant bevirimat resistance mutations revealed by "deep" sequencing of serially passaged, quasispecies-containing recombinant HIV-1A single polymorphism in HIV-1 subtype C SP1 is sufficient to confer natural resistance to the maturation inhibitor bevirimatHIV type 1 Gag as a target for antiviral therapyVirus maturation as a new HIV-1 therapeutic targetEbselen, a Small-Molecule Capsid Inhibitor of HIV-1 Replication.Structural and functional insights into the HIV-1 maturation inhibitor binding pocketMechanistic Studies and Modeling Reveal the Origin of Differential Inhibition of Gag Polymorphic Viruses by HIV-1 Maturation InhibitorsIonic liquid solutions as extractive solvents for value-added compounds from biomassStructure-Activity Relationships of the Human Immunodeficiency Virus Type 1 Maturation Inhibitor PF-46396The Second-Generation Maturation Inhibitor GSK3532795 Maintains Potent Activity Toward HIV Protease Inhibitor-Resistant Clinical IsolatesNovel approaches to inhibiting HIV-1 replication.Virtual screening based identification of novel small-molecule inhibitors targeted to the HIV-1 capsid.Anti-AIDS agents 81. Design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitorsPolymorphisms in Gag spacer peptide 1 confer varying levels of resistance to the HIV- 1 maturation inhibitor bevirimatNon-linear mixed effects modeling of antiretroviral drug response after administration of lopinavir, atazanavir and efavirenz containing regimens to treatment-naïve HIV-1 infected patients.Inhibitory effect of aqueous Dandelion extract on HIV-1 replication and reverse transcriptase activityMetabolic and functional diversity of saponins, biosynthetic intermediates and semi-synthetic derivativesConjugates of betulin derivatives with AZT as potent anti-HIV agents.HIV entry inhibitors and their potential in HIV therapyBevirimat: a novel maturation inhibitor for the treatment of HIV-1 infection.New betulinic acid derivatives as potent proteasome inhibitorsHIV-1 Gag as an Antiviral Target: Development of Assembly and Maturation Inhibitors.Identification of an HIV-1 Mutation in Spacer Peptide 1 That Stabilizes the Immature CA-SP1 Lattice.HIV-1 antiretroviral drug therapy.Identification and Characterization of BMS-955176, a Second-Generation HIV-1 Maturation Inhibitor with Improved Potency, Antiviral Spectrum, and Gag Polymorphic Coverage.Anti-AIDS agents 88. Anti-HIV conjugates of betulin and betulinic acid with AZT prepared via click chemistrySynthesis of betulinic acid derivatives as entry inhibitors against HIV-1 and bevirimat-resistant HIV-1 variantsAnti-AIDS agents 90. novel C-28 modified bevirimat analogues as potent HIV maturation inhibitors.HIV-1 Capsid Inhibitors as Antiretroviral AgentsCritical role of conserved hydrophobic residues within the major homology region in mature retroviral capsid assembly.New betulinic acid derivatives for bevirimat-resistant human immunodeficiency virus type-1.Recent progress in antiretrovirals--lessons from resistanceDiscovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity.Isolation and characterization of a small antiretroviral molecule affecting HIV-1 capsid morphology.Impact of human immunodeficiency virus type 1 resistance to protease inhibitors on evolution of resistance to the maturation inhibitor bevirimat (PA-457)Anti-AIDS agents. 78. Design, synthesis, metabolic stability assessment, and antiviral evaluation of novel betulinic acid derivatives as potent anti-human immunodeficiency virus (HIV) agentsNew small-molecule inhibitor class targeting human immunodeficiency virus type 1 virion maturation.Insights into the activity of maturation inhibitor PF-46396 on HIV-1 clade CPediatric antiretroviral therapy.
P2860
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P2860
Phase I and II study of the safety, virologic effect, and pharmacokinetics/pharmacodynamics of single-dose 3-o-(3',3'-dimethylsuccinyl)betulinic acid (bevirimat) against human immunodeficiency virus infection
description
2007 nî lūn-bûn
@nan
2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Phase I and II study of the sa ...... munodeficiency virus infection
@ast
Phase I and II study of the sa ...... munodeficiency virus infection
@en
Phase I and II study of the sa ...... munodeficiency virus infection
@nl
type
label
Phase I and II study of the sa ...... munodeficiency virus infection
@ast
Phase I and II study of the sa ...... munodeficiency virus infection
@en
Phase I and II study of the sa ...... munodeficiency virus infection
@nl
prefLabel
Phase I and II study of the sa ...... munodeficiency virus infection
@ast
Phase I and II study of the sa ...... munodeficiency virus infection
@en
Phase I and II study of the sa ...... munodeficiency virus infection
@nl
P2093
P2860
P921
P3181
P356
P1476
Phase I and II study of the sa ...... munodeficiency virus infection
@en
P2093
Abayomi Ogundele
Alan Forrest
David E Martin
Graham P Allaway
John Wilton
Karl Salzwedel
Patrick F Smith
P2860
P304
P3181
P356
10.1128/AAC.00152-07
P407
P577
2007-10-01T00:00:00Z