Search Results - "Hendrickson, T F"
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Structure-Assisted Design of Mechanism-Based Irreversible Inhibitors of Human Rhinovirus 3C Protease with Potent Antiviral Activity against Multiple Rhinovirus Serotypes
Published in Proceedings of the National Academy of Sciences - PNAS (28-09-1999)“…Human rhinoviruses, the most important etiologic agents of the common cold, are messenger-active single-stranded monocistronic RNA viruses that have evolved a…”
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Design, Synthesis, and Evaluation of Nonpeptidic Inhibitors of Human Rhinovirus 3C Protease
Published in Journal of medicinal chemistry (20-12-1996)“…The design, synthesis, and biological evaluation of reversible, nonpeptidic inhibitors of human rhinovirus (HRV) 3C protease (3CP) are reported. A novel series…”
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Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 4. Incorporation of P1 Lactam Moieties as l-Glutamine Replacements
Published in Journal of medicinal chemistry (08-04-1999)“…The structure-based design, chemical synthesis, and biological evaluation of various human rhinovirus (HRV) 3C protease (3CP) inhibitors which incorporate P1…”
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Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 6. Structure−Activity Studies of Orally Bioavailable, 2-Pyridone-Containing Peptidomimetics
Published in Journal of medicinal chemistry (11-04-2002)“…The structure-based design, chemical synthesis, and biological evaluation of various 2-pyridone-containing human rhinovirus (HRV) 3C protease (3CP) inhibitors…”
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Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease: Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P1 Glutamine Isosteric Replacements
Published in Journal of medicinal chemistry (16-07-1998)“…The investigation of tripeptide aldehydes as reversible covalent inhibitors of human rhinovirus (HRV) 3C protease (3CP) is reported. Molecular models based on…”
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Substituted Benzamide Inhibitors of Human Rhinovirus 3C Protease: Structure-Based Design, Synthesis, and Biological Evaluation
Published in Journal of medicinal chemistry (04-05-2000)“…A series of nonpeptide benzamide-containing inhibitors of human rhinovirus (HRV) 3C protease was identified using structure-based design. The design,…”
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Interaction of a Novel GDP Exchange Inhibitor with the Ras Protein
Published in Biochemistry (Easton) (10-11-1998)“…Mutated, tumorigenic Ras is present in a variety of human tumors. Compounds that inhibit tumorigenic Ras function may be useful in the treatment of Ras-related…”
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Experimental and computer modeling studies of micellar diastereoselectivity
Published in Journal of the American Chemical Society (01-07-1987)Get full text
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Backbone entropy of loops as a measure of their flexibility: Application to a Ras protein simulated by molecular dynamics
Published in Proteins, structure, function, and bioinformatics (01-10-1997)“…The flexibility of surface loops plays an important role in protein–protein and protein–peptide recognition; it is commonly studied by Molecular Dynamics or…”
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Esterolytic chemistry of vesicular thiocholine surfactant
Published in Journal of the American Chemical Society (01-09-1986)Get full text
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Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 4. Incorporation of P sub(1) Lactam Moieties as L-Glutamine Replacements
Published in Journal of medicinal chemistry (01-04-1999)“…The structure-based design, chemical synthesis, and biological evaluation of various human rhinovirus (HRV) 3C protease (3CP) inhibitors which incorporate P…”
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Structure-Based Design of a Parallel Synthetic Array Directed Toward the Discovery of Irreversible Inhibitors of Human Rhinovirus 3C Protease
Published in Journal of medicinal chemistry (09-05-2002)“…Utilizing the tools of parallel synthesis and structure-based design, a new class of Michael acceptor-containing, irreversible inhibitors of human rhinovirus…”
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Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease: Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P sub(1) Glutamine Isosteric Replacements
Published in Journal of medicinal chemistry (01-07-1998)“…The investigation of tripeptide aldehydes as reversible covalent inhibitors of human rhinovirus (HRV) 3C protease (3CP) is reported. Molecular models based on…”
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Electrostatic contributions to solvation energies: comparison of free energy perturbation and continuum calculations
Published in Journal of the American Chemical Society (01-02-1991)Get full text
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