Lucjusz Zaprutko
Lucjusz Zaprutko
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Synthesis of novel thiazolone-based compounds containing pyrazoline moiety and evaluation of their anticancer activity
D Havrylyuk, B Zimenkovsky, O Vasylenko, L Zaprutko, A Gzella, R Lesyk
European journal of medicinal chemistry 44 (4), 1396-1404, 2009
New 5-substituted thiazolo [3, 2-b][1, 2, 4] triazol-6-ones: synthesis and anticancer evaluation
R Lesyk, O Vladzimirska, S Holota, L Zaprutko, A Gzella
European journal of medicinal chemistry 42 (5), 641-648, 2007
A facile synthesis and anticancer activity evaluation of spiro [thiazolidinone-isatin] conjugates
D Kaminskyy, D Khyluk, O Vasylenko, L Zaprutko, R Lesyk
Scientia pharmaceutica 79 (4), 763-778, 2011
Synthesis of some N-substituted nitroimidazole derivatives as potential antioxidant and antifungal agents
D Olender, J Żwawiak, V Lukianchuk, R Lesyk, A Kropacz, A Fojutowski, ...
European journal of medicinal chemistry 44 (2), 645-652, 2009
Synthesis of new potential anticancer agents based on 4-thiazolidinone and oleanane scaffolds
D Kaminskyy, B Bednarczyk-Cwynar, O Vasylenko, O Kazakova, ...
Medicinal Chemistry Research 21 (11), 3568-3580, 2012
Multidirectional efficacy of biologically active nitro compounds included in medicines
D Olender, J Żwawiak, L Zaprutko
Pharmaceuticals 11 (2), 54, 2018
Methyl 3-hydroxyimino-11-oxoolean-12-en-28-oate (HIMOXOL), a synthetic oleanolic acid derivative, induces both apoptosis and autophagy in MDA-MB-231 breast cancer cells
N Lisiak, A Paszel-Jaworska, B Bednarczyk-Cwynar, L Zaprutko, ...
Chemico-biological interactions 208, 47-57, 2014
Triterpenoids. Part 21: Oleanolic acid azaderivatives as percutaneous transport promoters
L Zaprutko, D Partyka, B Bednarczyk-Cwynar
Bioorganic & medicinal chemistry letters 14 (18), 4723-4726, 2004
The analgesic and anti-inflammatory effect of new oleanolic acid acyloxyimino derivative
B Bednarczyk-Cwynar, L Zaprutko, J Marciniak, G Lewandowski, M Szulc, ...
European journal of pharmaceutical sciences 47 (3), 549-555, 2012
Microwave assisted synthesis of fragrant jasmone heterocyclic analogues
A Pawełczyk, L Zaprutko
European journal of medicinal chemistry 41 (5), 586-591, 2006
Anticancer effect of A-ring or/and C-ring modified oleanolic acid derivatives on KB, MCF-7 and HeLa cell lines
B Bednarczyk–Cwynar, L Zaprutko, P Ruszkowski, B Hładoń
Organic & biomolecular chemistry 10 (11), 2201-2205, 2012
Recent advances in synthesis and biological activity of triterpenic acylated oximes
B Bednarczyk-Cwynar, L Zaprutko
Phytochemistry Reviews 14 (2), 203-231, 2015
Targeting Nrf2-mediated gene transcription by triterpenoids and their derivatives
A Loboda, E Rojczyk-Golebiewska, B Bednarczyk-Cwynar, Z Lucjusz, ...
Biomolecules & therapeutics 20 (6), 499, 2012
Strong and long-lasting antinociceptive and anti-inflammatory conjugate of naturally occurring oleanolic acid and aspirin
B Bednarczyk-Cwynar, N Wachowiak, M Szulc, E Kamińska, A Bogacz, ...
Frontiers in pharmacology 7, 202, 2016
Nitrogenous triterpene derivatives. 10. Hemisuccinates of some oleanolic acid derivatives and their antiulcer effect
U Wrzeciono, I Malecki, J Budzianowski, H Kierylowicz, L Zaprutko, ...
Die Pharmazie 40 (8), 542-544, 1985
Beckmann rearrangement of oxime obtained from oleanolic acid. Structure elucidation of the initial oxime
B Bednarczyk-Cwynar, L Zaprutko, A Froelich
Journal of Molecular Structure 1053, 115-121, 2013
A brief history of taxol
J Żwawiak, L Zaprutko
Journal of Medical Science 83 (1), 47-52, 2014
Synthesis of triterpenoid acylates: effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses
OB Kazakova, NI Medvedeva, IP Baikova, GA Tolstikov, TV Lopatina, ...
Russian journal of bioorganic chemistry 36 (6), 771-778, 2010
Molecular consortia—Various structural and synthetic concepts for more effective therapeutics synthesis
A Pawełczyk, K Sowa-Kasprzak, D Olender, L Zaprutko
International journal of molecular sciences 19 (4), 1104, 2018
Azoles. 27. Nitroimidazole derivatives, their antibacterial and fungicidal activity and electron affinity
L Zaprutko, M Gajdziński, W Michalska, K Pietkiewicz, K Lutomski, ...
Die Pharmazie 44 (12), 817-820, 1989
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