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Martin Empting

Showing results (1-10 of 80) with videos related to

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Future Medicinal Chemistry|May 26, 2021
KSHV-specific antivirals targeting the protein-DNA interaction of the latency-associated nuclear antigenAylin Berwanger, Martin Empting
Beilstein Journal of Organic Chemistry|November 10, 2018
Targeting the <i>Pseudomonas</i> quinolone signal quorum sensing system for the discovery of novel anti-infective pathoblockersChristian Schütz, Martin Empting
Journal of Peptide Science : an Official Publication of the European Peptide Society|April 12, 2014
Potent inhibitors of human matriptase-1 based on the scaffold of sunflower trypsin inhibitorHeiko Fittler, Olga Avrutina, Martin Empting, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2019
Restriction-Free Construction of a Phage-Presented Very Short Macrocyclic Peptide LibraryValentin Jakob, Saskia Helmsing, Michael Hust, et al.
European Journal of Medicinal Chemistry|December 2, 2014
Catechol-based substrates of chalcone synthase as a scaffold for novel inhibitors of PqsDGiuseppe Allegretta, Elisabeth Weidel, Martin Empting, et al.
Organic & Biomolecular Chemistry|August 21, 2012
Between two worlds: a comparative study on in vitro and in silico inhibition of trypsin and matriptase by redox-stable SFTI-1 variants at near physiological pHOlga Avrutina, Heiko Fittler, Bernhard Glotzbach, et al.
Organic & Biomolecular Chemistry|January 31, 2013
Combinatorial tuning of peptidic drug candidates: high-affinity matriptase inhibitors through incremental structure-guided optimizationHeiko Fittler, Olga Avrutina, Bernhard Glotzbach, et al.
Molecules (Basel, Switzerland)|November 30, 2019
Concepts and Core Principles of Fragment-Based Drug DesignPhiline Kirsch, Alwin M Hartman, Anna K H Hirsch, et al.
Future Medicinal Chemistry|December 23, 2014
Composing compound libraries for hit discovery--rationality-driven preselection or random choice by structural diversity?Elisabeth Weidel, Matthias Negri, Martin Empting, et al.
Immunopharmacology and Immunotoxicology|November 10, 2015
Single-domain antibodies for biomedical applicationsSimon Krah, Christian Schröter, Stefan Zielonka, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Future Medicinal Chemistry|May 26, 2021
KSHV-specific antivirals targeting the protein-DNA interaction of the latency-associated nuclear antigenAylin Berwanger, Martin Empting
Beilstein Journal of Organic Chemistry|November 10, 2018
Targeting the <i>Pseudomonas</i> quinolone signal quorum sensing system for the discovery of novel anti-infective pathoblockersChristian Schütz, Martin Empting
Journal of Peptide Science : an Official Publication of the European Peptide Society|April 12, 2014
Potent inhibitors of human matriptase-1 based on the scaffold of sunflower trypsin inhibitorHeiko Fittler, Olga Avrutina, Martin Empting, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2019
Restriction-Free Construction of a Phage-Presented Very Short Macrocyclic Peptide LibraryValentin Jakob, Saskia Helmsing, Michael Hust, et al.
European Journal of Medicinal Chemistry|December 2, 2014
Catechol-based substrates of chalcone synthase as a scaffold for novel inhibitors of PqsDGiuseppe Allegretta, Elisabeth Weidel, Martin Empting, et al.
Organic & Biomolecular Chemistry|August 21, 2012
Between two worlds: a comparative study on in vitro and in silico inhibition of trypsin and matriptase by redox-stable SFTI-1 variants at near physiological pHOlga Avrutina, Heiko Fittler, Bernhard Glotzbach, et al.
Organic & Biomolecular Chemistry|January 31, 2013
Combinatorial tuning of peptidic drug candidates: high-affinity matriptase inhibitors through incremental structure-guided optimizationHeiko Fittler, Olga Avrutina, Bernhard Glotzbach, et al.
Molecules (Basel, Switzerland)|November 30, 2019
Concepts and Core Principles of Fragment-Based Drug DesignPhiline Kirsch, Alwin M Hartman, Anna K H Hirsch, et al.
Future Medicinal Chemistry|December 23, 2014
Composing compound libraries for hit discovery--rationality-driven preselection or random choice by structural diversity?Elisabeth Weidel, Matthias Negri, Martin Empting, et al.
Immunopharmacology and Immunotoxicology|November 10, 2015
Single-domain antibodies for biomedical applicationsSimon Krah, Christian Schröter, Stefan Zielonka, et al.
Pageof 8