Abstract
Our structure-based design strategies which specifically target the HIV-1 protease backbone, resulted in a number of exceedingly potent nonpeptidyl inhibitors. One of these inhibitors, darunavir (TMC114), contains a privileged, structure-based designed high-affinity P2 ligand, 3(R),3a(S),6a(R)-bis-tetrahydrofuranylurethane (bis-THF). Darunavir has recently been approved for the treatment of HIV/AIDS patients harboring multidrug-resistant HIV-1 variants that do not respond to previously existing HAART regimens.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, N.I.H., Intramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Clinical Trials as Topic
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Crystallography, X-Ray
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Darunavir
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Drug Design*
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Drug Resistance, Viral*
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HIV Infections / drug therapy*
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HIV Protease Inhibitors / chemistry
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HIV Protease Inhibitors / therapeutic use
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HIV-1 / drug effects*
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Humans
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Ligands
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Molecular Structure
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Structure-Activity Relationship
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Sulfonamides / chemistry*
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Sulfonamides / therapeutic use
Substances
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HIV Protease Inhibitors
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Ligands
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Sulfonamides
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Darunavir