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Chemistry & Biology|September 1, 2015
Identification and Characterization of an Irreversible Inhibitor of CDK2Elizabeth Anscombe, Elisa Meschini, Regina Mora-Vidal, et al.Bioorganic & Medicinal Chemistry|June 30, 2012
Experimental and 'in silico' analysis of the effect of pH on HIV-1 protease inhibitor affinity: implications for the charge state of the protein ionogenic groupsJosé L Domínguez, Thomas Gossas, M Carmen Villaverde, et al.Antiviral Research|January 12, 2013
Resolution of the interaction mechanisms and characteristics of non-nucleoside inhibitors of hepatitis C virus polymeraseJohan Winquist, Eldar Abdurakhmanov, Vera Baraznenok, et al.Bioorganic & Medicinal Chemistry|June 6, 2003
Peptide-based inhibitors of hepatitis C virus full-length NS3 (protease-helicase/NTPase): model compounds towards small molecule inhibitorsKarin Oscarsson, Anton Poliakov, Stefan Oscarson, et al.Journal of Medicinal Chemistry|February 12, 2014
Identification of weak points of hepatitis C virus NS3 protease inhibitors using surface plasmon resonance biosensor-based interaction kinetic analysis and genetic variantsSofia Svahn Gustafsson, Angelica Ehrenberg, Benjamin Schmuck, et al.Biochemistry|October 14, 2024
Unraveling the Bivalent and Rapid Interactions Between a Multivalent RNA Recognition Motif and RNA: A Kinetic ApproachGuillermo Pérez-Ropero, Anna Pérez-Ràfols, Tommasso Martelli, et al.Biochemical Pharmacology|July 6, 2010
Inhibition of HIV-1 by non-nucleoside reverse transcriptase inhibitors via an induced fit mechanism-Importance of slow dissociation and relaxation rates for antiviral efficacyMalin Elinder, Philippe Selhorst, Guido Vanham, et al.Biochemical Pharmacology|April 26, 2012
Histaminergic pharmacology of homo-oligomeric β3 γ-aminobutyric acid type A receptors characterized by surface plasmon resonance biosensor technologyChristian Seeger, Tony Christopeit, Karoline Fuchs, et al.Bioorganic & Medicinal Chemistry|April 25, 2008
Beta-amino acid substitutions and structure-based CoMFA modeling of hepatitis C virus NS3 protease inhibitorsJohanna Nurbo, Shane D Peterson, Göran Dahl, et al.Biomolecules|December 23, 2023
The Allosteric Regulation of Β-Ureidopropionase Depends on Fine-Tuned Stability of Active-Site Loops and Subunit InterfacesDaniela Cederfelt, Dilip Badgujar, Ayan Au Musse, et al.Pageof 13