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Discovery of cyclic sulfone hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors: structure-based design and in vivo reduction of amyloid β-peptides. [electronic resource] by
- Rueeger, Heinrich
- Lueoend, Rainer
- Rogel, Olivier
- Rondeau, Jean-Michel
- Möbitz, Henrik
- Machauer, Rainer
- Jacobson, Laura
- Staufenbiel, Matthias
- Desrayaud, Sandrine
- Neumann, Ulf
Producer: 20120831
In:
Journal of medicinal chemistry vol. 55
Availability: No items available.
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13.
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Discovery of cyclic sulfoxide hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors: structure based design and in vivo reduction of amyloid β-peptides. [electronic resource] by
- Rueeger, Heinrich
- Lueoend, Rainer
- Machauer, Rainer
- Veenstra, Siem Jacob
- Jacobson, Laura Helen
- Staufenbiel, Matthias
- Desrayaud, Sandrine
- Rondeau, Jean-Michel
- Möbitz, Henrik
- Neumann, Ulf
Producer: 20140407
In:
Bioorganic & medicinal chemistry letters vol. 23
Availability: No items available.
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New Potent DOT1L Inhibitors for [electronic resource] by
- Stauffer, Frédéric
- Weiss, Andreas
- Scheufler, Clemens
- Möbitz, Henrik
- Ragot, Christian
- Beyer, Kim S
- Calkins, Keith
- Guthy, Daniel
- Kiffe, Michael
- Van Eerdenbrugh, Bernard
- Tiedt, Ralph
- Gaul, Christoph
Publication details: ACS medicinal chemistry letters Dec 2019
In:
ACS medicinal chemistry letters vol. 10
Availability: No items available.
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16.
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In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part II. [electronic resource] by
- Revesz, Laszlo
- Schlapbach, Achim
- Aichholz, Reiner
- Dawson, Janet
- Feifel, Roland
- Hawtin, Stuart
- Littlewood-Evans, Amanda
- Koch, Guido
- Kroemer, Markus
- Möbitz, Henrik
- Scheufler, Clemens
- Velcicky, Juraj
- Huppertz, Christine
Producer: 20101123
In:
Bioorganic & medicinal chemistry letters vol. 20
Availability: No items available.
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17.
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In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part I. [electronic resource] by
- Revesz, Laszlo
- Schlapbach, Achim
- Aichholz, Reiner
- Feifel, Roland
- Hawtin, Stuart
- Heng, Richard
- Hiestand, Peter
- Jahnke, Wolfgang
- Koch, Guido
- Kroemer, Markus
- Möbitz, Henrik
- Scheufler, Clemens
- Velcicky, Juraj
- Huppertz, Christine
Producer: 20101123
In:
Bioorganic & medicinal chemistry letters vol. 20
Availability: No items available.
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18.
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The Crystal Structure of Cancer Osaka Thyroid Kinase Reveals an Unexpected Kinase Domain Fold. [electronic resource] by
- Gutmann, Sascha
- Hinniger, Alexandra
- Fendrich, Gabriele
- Drückes, Peter
- Antz, Sylvie
- Mattes, Henri
- Möbitz, Henrik
- Ofner, Silvio
- Schmiedeberg, Niko
- Stojanovic, Aleksandar
- Rieffel, Sebastien
- Strauss, André
- Troxler, Thomas
- Glatthar, Ralf
- Sparrer, Helmut
Producer: 20150910
In:
The Journal of biological chemistry vol. 290
Availability: No items available.
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19.
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Discovery of Potent, Selective, and Structurally Novel Dot1L Inhibitors by a Fragment Linking Approach. [electronic resource] by
- Möbitz, Henrik
- Machauer, Rainer
- Holzer, Philipp
- Vaupel, Andrea
- Stauffer, Frédéric
- Ragot, Christian
- Caravatti, Giorgio
- Scheufler, Clemens
- Fernandez, Cesar
- Hommel, Ulrich
- Tiedt, Ralph
- Beyer, Kim S
- Chen, Chao
- Zhu, Hugh
- Gaul, Christoph
Publication details: ACS medicinal chemistry letters Mar 2017
In:
ACS medicinal chemistry letters vol. 8
Availability: No items available.
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20.
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Discovery of Imidazoquinolines as a Novel Class of Potent, Selective, and in Vivo Efficacious Cancer Osaka Thyroid (COT) Kinase Inhibitors. [electronic resource] by
- Glatthar, Ralf
- Stojanovic, Aleksandar
- Troxler, Thomas
- Mattes, Henri
- Möbitz, Henrik
- Beerli, Rene
- Blanz, Joachim
- Gassmann, Ernst
- Drückes, Peter
- Fendrich, Gabriele
- Gutmann, Sascha
- Martiny-Baron, Georg
- Spence, Fiona
- Hornfeld, Jeff
- Peel, John Edmonson
- Sparrer, Helmut
Producer: 20170606
In:
Journal of medicinal chemistry vol. 59
Availability: No items available.
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