Publications by authors named "Marta Bugaj"

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Discovery of a series of ester-substituted NLRP3 inflammasome inhibitors.
David Harrison, Nicolas Boutard, Krzysztof Brzozka, Marta Bugaj, Stefan Chmielewski

Bioorg Med Chem Lett· December 2020

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N-Arylation of Diketopyrrolopyrroles with Aryl Triflates.
Krzysztof Gutkowski, Kamil Skonieczny, Marta Bugaj, Denis Jacquemin, Daniel T Gryko

Chem Asian J· April 2020

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5-Keto-3-cyano-2,4-diaminothiophenes as selective maternal embryonic leucine zipper kinase inhibitors.
Nicolas Boutard, Aleksandra Sabiniarz, Klaudia Czerwińska, Małgorzata Jarosz, Anna Cierpich, Marta Bugaj

Bioorg Med Chem Lett· February 2019

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A novel, dual pan-PIM/FLT3 inhibitor SEL24 exhibits broad therapeutic potential in acute myeloid leukemia.
Wojciech Czardybon, Renata Windak, Aniela Gołas, Michał Gałęzowski, Aleksandra Sabiniarz, Marta Bugaj

Oncotarget· March 2018

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Electron ionization and electrospray mass spectra of diaryl-substituted enaminoketones and their thio analogs.
Beata Wileńska, Witold Danikiewicz, Marta Bugaj, Krystyna Kamieńska-Trela, Adam Krówczyńsk

Eur J Mass Spectrom (Chichester)· February 2012

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Structural studies on aryl-substituted enaminoketones and their thio analogues. Part I. Analysis of high-resolution (1)H, (13)C NMR and (13)C CP MAS spectra combined with GIAO-DFT calculations.
Marta Bugaj, Piotr A Baran, Piotr Bernatowicz, Patrycja Brozek, Krystyna Kamieńska-Trela

Magn Reson Chem· October 2009

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Structural studies on aryl-substituted enaminoketones and their thio analogues. Part II. Experimental and DFT calculated carbon-carbon coupling constants, (n)J(CC)'s (n = 1-3).
Marta Bugaj, Piotr A Baran, Krystyna Kamieńska-Trela, Adam Krówczyński

Magn Reson Chem· October 2009

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Synthesis and biological activity of N(alpha)-[4-[N-[(3,4-dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl]-N-propargylamino]phenylacetyl]-L-glutamic acid.
Anna Kusakiewicz-Dawid, Marta Bugaj, Jolanta M Dzik, Barbara Gołos, Patrycja Wińska

Acta Biochim Pol· January 2003

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