A False-Positive Screening Hit in Fragment-Based Lead Discovery: Watch out for the Red Herring.
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 7, p. 1908, doi. 10.1002/anie.201609824
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- Publication type:
- Article
Works matching DE "ENDOTHIAPEPSIN"
Results: 6
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Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment-Based Drug Design Facilitated by Dynamic Combinatorial Chemistry.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 32, p. 9422, doi. 10.1002/anie.201603074
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- Article
3
Tracing Binding Modes in Hit-to-Lead Optimization: Chameleon-Like Poses of Aspartic Protease Inhibitors.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 9, p. 2849, doi. 10.1002/anie.201411206
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- Publication type:
- Article
4
Structure-Based Design of Inhibitors of the Aspartic Protease Endothiapepsin by Exploiting Dynamic Combinatorial Chemistry.
- Published in:
- Angewandte Chemie International Edition, 2014, v. 53, n. 12, p. 3259, doi. 10.1002/anie.201309682
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- Publication type:
- Article
5
Structure-Based Optimization of Inhibitors of the Aspartic Protease Endothiapepsin.
- Published in:
- International Journal of Molecular Sciences, 2015, v. 16, n. 8, p. 19184, doi. 10.3390/ijms160819184
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- Article
6
Structures of endothiapepsin-fragment complexes from crystallographic fragment screening using a novel, diverse and affordable 96-compound fragment library.
- Published in:
- Acta Crystallographica: Section F, Structural Biology Communications, 2016, v. 72, n. 5, p. 346, doi. 10.1107/S2053230X16004623
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- Publication type:
- Article