Publications by authors named "Beata Labuzek"

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Nutlin-3a-aa: Improving the Bioactivity of a p53/MDM2 Interaction Inhibitor by Introducing a Solvent-Exposed Methylene Group.
Florian Nietzold, Stefan Rubner, Beata Labuzek, Przemysław Golik, Ewa Surmiak

Chembiochem· March 2023

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Multicomponent Peptide Stapling as a Diversity-Driven Tool for the Development of Inhibitors of Protein-Protein Interactions.
Manuel G Ricardo, Ameena M Ali, Jacek Plewka, Ewa Surmiak, Beata Labuzek

Angew Chem Int Ed Engl· March 2020

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Optimized Inhibitors of MDM2 via an Attempted Protein-Templated Reductive Amination.
Ramon van der Vlag, M Yagiz Unver, Tommaso Felicetti, Aleksandra Twarda-Clapa, Fatima Kassim, Beata Labuzek

ChemMedChem· February 2020

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A fluorinated indole-based MDM2 antagonist selectively inhibits the growth of p53 osteosarcoma cells.
Lukasz Skalniak, Aleksandra Twarda-Clapa, Constantinos G Neochoritis, Ewa Surmiak, Monika Machula, Beata Labuzek

FEBS J· April 2019

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NMR fragment-based screening for development of the CD44-binding small molecules.
Marcin Pustuła, Mirosława Czub, Beata Łabuzek, Ewa Surmiak, Marcin Tomala

Bioorg Chem· February 2019

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Design of indole- and MCR-based macrocycles as p53-MDM2 antagonists.
Constantinos G Neochoritis, Maryam Kazemi Miraki, Eman M M Abdelraheem, Ewa Surmiak, Tryfon Zarganes-Tzitzikas

Beilstein J Org Chem· February 2019

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Crystal structure of the FAS1 domain of the hyaluronic acid receptor stabilin-2.
Aleksandra Twarda-Clapa, Beata Labuzek, Dobroslawa Krzemien, Bogdan Musielak, Przemyslaw Grudnik

Acta Crystallogr D Struct Biol· July 2018

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1,4,5-Trisubstituted Imidazole-Based p53-MDM2/MDMX Antagonists with Aliphatic Linkers for Conjugation with Biological Carriers.
Aleksandra Twarda-Clapa, Sylwia Krzanik, Katarzyna Kubica, Katarzyna Guzik, Beata Labuzek

J Med Chem· May 2017

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