Department of Organic Chemistry
Faculty of Pharmacy
PUBLICATION ACTIVITIES
Main publications:
- Fedorowicz, J, Sączewski, J., Drażba, Z., Wiśniewska, P., Gdaniec, M., Wicher, B., Suwiński, G., Jalińska, A.
Synthesis and fluorescence of dihydro-[1,2,4]triazolo[4,3-a]pyridin-2-ium-carboxylates: An experimental and TD-DFT comparative study;
Dyes and Pigments 161 (2019), p. 347-359,
(go to article) - Fedorowicz, J., Sączewski, J., Konopacka, A., Waleron, K., Lejnowski, D., Ciura, K., Tomašič, T., Skok, Ž., Savijoki, K., Morawska, M.,Gilbert-Girard, S., Fallarero, A.
Synthesis and biological evaluation of hybrid quinolone-based quaternary ammonium antibacterial agents;
European Journal of Medicinal Chemistry 179, (2019), pp. 576-590,
(go to article) - Fedorowicz, J., Gzella, K., Wiśniewska, P., Sączewski, J.
2,2’-[(1,4-dimethoxy-1,4-dioxobutane-2,3-diylidene)bis(azanylylidene)]bis(quinoline-3-carboxylic acid);
MolBank. (2019), Article number M1093
(go to article) - Makowska, A., Saczewski, F., Bednarski, P.J., Saczewski, J., Balewski, Ł.
Hybrid molecules composed of 2,4-diamino-1,3,5-triazines and 2-imino-coumarins and coumarins. Synthesis and cytotoxic properties;
Molecules. 23 (2018), 1616,
(go to article) - Mazur, L., Saczewski, J., Jarzembska, K.N., Szwarc-Karabyka, K., Paprocka, R., Modzelewska-Banachiewicz, B.;
Synthesis, structural characterization and reactivity of new trisubstituted: N 1-acylamidrazones: Solid state and solution studies;
CrystEngComm. 20 (2018), 4179-4193,
(go to article) - Fedorowicz, J., Sączewski, J.
Modifications of quinolones and fluoroquinolones: hybrid compounds and dual-action molecules;
Monatshefte fur Chemie. 149 (2018), 1199-1245,
(go to article) - Krause, M., Foks, H., Augustynowicz-Kopeć, E., Napiórkowska, A., Szczesio, M., Gobis, K.
Synthesis and tuberculostatic activity evaluation of novel benzazoles with alkyl, cycloalkyl or pyridine moiety;
Molecules. 23 (2018), 985,
(go to article) - Szczesio, M., Gołka, J., Korona-Głowniak, I.,Gobis, K.,
Planarity of benzoyldithiocarbazate tuberculostatics.V antibacterial activities of diesters of benzoyldithiocarbazic acid;
Journal of Molecular Structure. 1167 (2018), 127-133,
(go to article) - Szczesio, M., Gołka, J., Korona-Głowniak, I., Orlewska, C., Gobis, K., Olczak, A.
Planarity of heteroaryldithiocarbazic acid derivatives showing tuberculostatic activity: Structure-activity relationships;
Acta Crystallographica Section C: Structural Chemistry. 74 (2018), 400-405,
(go to article) - Główka M.L., Kałużyńska S., Krause, M., Gobis, K., Foks, H., Szczesio, M., Olczak, A ;
SThe structures of benzimidazole derivatives and their potential as tuberculostatics;
Acta Crystallographica Section C: Structural Chemistry. 74 (2018), 1684-1691,
(go to article) - Pogorzelska A., Żołnowska B., Bartoszewski R.;
Cysteine cathepsins as a prospective target for anticancer therapies—current progress and prospects;
Biochimie 151 (2018) 85-106,
(go to article) - Kawczak P., Belka M, Sławiński J, Bączek T.;
QSRR evaluation of the new anticancer sulfonamides in view of the cis-trans isomerism
Current Pharmaceutical Analysis 14 (2018) 35-40,
(go to article) - Pogorzelska A., Żołnowska B., Sławiński J., Kawiak A., Szafrański K., Belka M., Bączek T.;
Synthesis of 2-alkylthio-N-(quinazolin-2-yl)benzenesulfonamide derivatives: anticancer activity, QSAR studies, and metabolic stability;
Monatshefte fur Chemie 149 (2018) 1885-1898,
(go to article) - Pogorzelska A., Sławiński J., Kawiak A., Żołnowska B., Chojnacki J.,, Stasiłojć G., Ulenberg S., Szafrański K., Bączek T.; ISynthesis, molecular structure, and metabolic stability of new series of N’-(2-alkylthio-4-chloro-5-methylbenzenesulfonyl)-1-(5-phenyl-1H-pyrazol-1-yl)amidine as potential anti-cancer agents; European Journal of Medicinal Chemistry 155 (2018) 670-680, (go to article)
- Zuvela P., Liu J., Myunggi Y., Pomastowski P., Sagandykova G., Belka M., David J., Bączek T., Krzysztof Szafrański, Beata Żołnowska, Jarosław Sławiński, Supuran C., Wong M., Buszewski B.; Target-based drug discovery through inversion of quantitative structure-drug property relationships and molecular simulation: CA IX-sulphonamide complexes. J. Enz. Inhib. Med. Chem. 33 (2018) 1430‒1443; (go to article)
- Cieślik P., Woźniak M., Tokarski K., Kusek M., Pilca A., Płoska A., Radulska A., Pelikant-Małecka I, Beata Żołnowska, Jarosław Sławiński, Kalinowski L., Wierońska J.; Simultaneous activation of muscarinic and GABAB receptors as a bidirectional target for novel antipsychotic. Behav. Brain Res. (2018), (go to article)
- Żołnowska, B.; Sławiński, J.; Brzozowski, Z.; Kawiak, A.; Belka, M.; Zielińska, J.; Baczek˛, T.; Chojnacki, J. Synthesis, molecular structure, anticancer activity, and QSAR study of N-(Aryl/heteroaryl)-4-(1h-pyrrol-1-yl)benzenesulfonamide derivatives. Int. J. Mol. Sci. 2018, 19, 1–23, (go to article)
- Monti, S. M.; Meccariello, A.; Ceruso, M.; Szafrański, K.; Sławiński, J.; Supuran, C. T. Inhibition studies of Brucella suis β-carbonic anhydrases with a series of 4-substituted pyridine-3-sulphonamides. J. Enzyme Inhib. Med. Chem. 2018, 33, (go to article)
- Żołnowska B., Sławiński J, Szafrański K., Angeli A, Supuran C.T., Kawiak A., Wieczór M., Zielińska J., Bączek T.; Novel 2-(2-arylmethylthio-4-chloro-5-methylbenzenesulfonyl)-1-(1,3,5-triazin-2-ylamino)guanidine derivatives: Inhibition of human carbonic anhydrase cytosolic isozymes I and II and the transmembrane tumor-associated isozymes IX and XII, anticancer activity, and molecular modeling studies; European Journal of Medicinal Chemistry 143 (2018) 1931-1941, (go to article)
- Szafrański K., Sławiński J., Kędzia A., Kwapisz E.; Syntheses of Novel 4-Substituted N-(5-amino-1H-1,2,4-triazol-3-yl)pyridine-3-sulfonamide Derivatives with Potential Antifungal Activity; Molecules 22 (11) (2017), art 1926, (go to article)
- Pogorzelska A., Żołnowska B., Sławiński J., Szafrański K., Kawiak A., Chojnacki J., Ulenberg S., Zielińska J.,Bączek T.; Novel 2-(2-alkylthiobenzenesulfonyl)-3-(phenylprop-2-ynylideneamino)guanidine derivatives as potent anticancer agents – Synthesis, molecular structure, QSAR studies and metabolic stability; European Journal of Medicinal Chemistry 138 (2017) 357-370, (go to article)
- J. Sączewski, J. Fedorowicz, M. Gdaniec, P. Wiśniewska, E. Sieniawska, Z.Drażba, J. Rzewnicka, Ł. Balewski ; The Elusive Paal–Knorr Intermediates in the Trofimov Synthesis of Pyrroles: Experimental and Theoretical Studies; Journal of Organic Chemistry. 82, 2017, 9737-9743(go to article)
- Sławiński J., Szafrański K., Pogorzelska A., Żołnowska B., Kawiak A., Macur K., Belka M., Bączek T.; Novel 2-benzylthio-5-(1,3,4-oxadiazol-2-yl)benzenesulfonamides with anticancer activity: Synthesis, QSAR study, and metabolic stability; European Journal of Medicinal Chemistry 132 (2017) 236-248, (go to article)
- Zołnowska B., Sławiński J., Pogorzelska A., Szafrański K., Kawiak A., Stasiłojć G., Belka M., Zielińska J., Bączek T.; Synthesis, QSAR studies, and metabolic stability of novel 2-alkylthio-4-chloro-N-(5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)benzenesulfonamide derivatives as potential anticancer and apoptosis-inducing agents; Chem Biol Drug Des. 2017;1–17. (go to article)
- Zołnowska B., Sławiński J., Pogorzelska A., Szafrański K., Kawiak A., Stasiłojć G., Belka M., Ulenberg S., Baczek T., Chojnacki J. Novel 5-substituted 2-(aylmethylthio)-4-chloro-N-(5-aryl-1,2,4-triazin-3-yl)benzenesulfonamides: Synthesis, molecular structure, anticancer activity, apoptosis-inducing activity and metabolic stability(Article) Molecules 21 (1) (2016), art 808, (go to article)
- J. Sławiński, A. Grzonek, B. Żołnowska, A. Kawiak; Synthesis of novel pyrido[4,3-e][1,2,4]triazino[3,2-c][1,2,4]thiadiazine 6,6-dioxide derivatives with potential anticancer activity; Molecules 21 (1) (2016), art 41, s. 1-16 (go to article)
- A. Pogorzelska, J. Sławiński, K. Brożewicz, Sz. Ulenberg, T. Bączek; Novel 3-Amino-6-chloro-7-(azol-2 or 5-yl)-1,1-dioxo-1,4,2-benzodithiazine Derivatives with Anticancer Activity: Synthesis and QSAR Study; Molecules 20(12) (2015), 21960-21970 (go to article)
- B. Żołnowska, J. Sławiński, A. Grzonek, A. Kędzia, E. Kwapisz, A. Kawiak; N-Substituted N′-(2-alkylthio-4-chloro-5-methylbenzenesulfonyl)guanidines – Antibacterial, Cytotoxic Activities and Some Structure-Activity Relationships; Pol. J. Microbiol. 63 (3) 2015 299-305; (go to article)
- B. Żołnowska, J. Sławiński, M. Belka, T. Bączek, A. Kawiak, J. chojnacki, A. Pogorzelska, K. Szafrański Synthesis, Molecular Structure, Metabolic Stability and QSAR Studies of a Novel Series of Anticancer N-Acylbenzenesulfonamides; Molecules 20(10) 2015, 19101-19129; (go to article)
- J. Sączewski, J. Fedorowicz, M. Korcz, F. Sączewski, B. Wicher, M. Gdaniec, A. Konopacka; Experimental and theoretical studies on the tautomerism and reactivity of isoxazolo[3,4-b]quinolin-3(1H)-ones; Tetrahedron. 2015; (go to article)
- A. Bułakowska, M. Konieczny; Synthesis of vinyl sulfones by ring opening of 4,4-dioxo-2,3-dihydrobenzo[b][1,4]oxathiines and their in situ reactions with nucleophilic or electrophilic agents; J. Het. Chem. 2015; vol. 52, nr 2, s. 440-444; (go to article)
- M. Konieczny, A. Bułakowska, D. Pirska, W. Konieczny, A. Składanowski, M. Sabisz, M. Wojciechowski, K. Lemke, A. Pieczykolan, W. Strożek, Structural factors affecting affinity of cytotoxic oxathiole-fused chalcones toward tubulin, Eur. J. Med. Chem. 2015; vol. 89, s. 733-742 (go to article)
- I. Łącka, M. Konieczny, A. Bułakowska, M. Kodedová, D. Gašková, I. K. Maurya, R. Prasad, S. Milewski, Chemosensitization of multidrug resistant Candida albicans by the oxathiolone fused chalcone derivatives, Front. Microbiol. 2015; vol. 6, art. 783 (go to article)
- K. Gobis H. Foks,M. Serocki, E. Augustynowicz-Kopeć, A. Napiórkowska ;Synthesis and evaluation of in vitro antimycobacterial activity of novel 1H-benzo[d]imidazole derivatives and analogues ; Eur. J. Med. Chem. 89 (2015), 13-20,
(go to article) - K.Szafrański, J. Sławiński, Synthesis of Novel 1-(4-Substituted pyridine-3-sulfonyl)-3-phenylureas with Potential Anticancer Activity; Molecules 20(7) 2015, 12029-12044 (go to full text)
- K. Gobis H. Foks, K. Suchan, E. Augustynowicz-Kopeć, A. Napiórkowska, K. Bojanowski ; Novel 2-(2-phenalkyl)-1H-benzo[d]imidazoles as antitubercular agents. Synthesis, biological evaluation and structure-activity relationship; Bioorg. Med. Chem. 23 (2015), 2112–2120,
(go to article) - J. Sławiński, B. Żołnowska, Z. Brzozowski, A. Kawiak, M. Belka, T. Bączek Synthesis and QSAR Study of Novel 6-Chloro-3-(2-Arylmethylene-1-methylhydrazino)-1,4,2-benzodithiazine 1,1-Dioxide Derivatives with Anticancer Activity; Molecules 20(4) 2015, 5754-5770 (go to full text)
- M.. Konieczny, A. Bułakowska, J. Polak, D. Pirska, W. Konieczny, P. Gryń, A. Składanowski, M. Sabisz, K. Lemke, A. Pieczykolan, M. Gałązka, K. Wiciejowska, J. Wietrzyk, Structural factors affecting cytotoxic activity of (E)-1-(benzo[d ][1,3]oxathiol-6-yl)-3-phenylprop-2-en-1-one derivatives, Chem. Biol. Drug Des. 2014; vol. 84, nr 1, 86-91 (go to article)
- B. Żołnowska, J. Sławiński, A. Pogorzelska, J. Chojnacki, D. Vullo, C.T. Supuran; Carbonic anhydrase inhibitors. Synthesis, and molecular structure of novel series N-substituted N′-(2-arylmethylthio-4-chloro-5- methylbenzenesulfonyl)guanidines and their inhibition of human cytosolic isozymes i and II and the transmembrane tumor-associated isozymes IX and XII; Eur. J. Med. Chem. 71 (2014), 135-147. (go to article)
- J. Sławiński, A. Pogorzelska, B. Żołnowska, A. Kędzia, M. Ziółkowska-Klinkosz, E. Kwapisz; Synthesis and Anti-Yeast Evaluation of Novel 2-Alkylthio-4-chloro-5-methyl-N-[imino-(1-oxo-(1H)-phthalazin-2-yl)methyl]benzenesulfonamide Derivatives; Molecules 19 (2014), 13704-13723 (go to article)
- E. Sikorska, M. Dawgul, K. Greber, E. Iłowska, A. Pogorzelska, W. Kamysz; Self-assembly and interactions of short antimicrobial cationic lipopeptides with membrane lipids: ITC, FTIR and molecular dynamics studies;BBA-Biomembranes 2625-2635. (go to article)
- M. Belka, W. Hewelt-Belka, J. Sławiński, T.Bączek; Mass Spectrometry Based Identification of Geometric Isomers during Metabolic Stability Study of a New Cytotoxic Sulfonamide Derivatives Supported by Quantitative Structure-Retention Relationships; PLOS ONE 9 (2014), e98096. (go to article)
- M. Konieczny, A. Bułakowska, J. Polak, D. Pirska, W. Konieczny, P. Gryń, A. Skladanowski, M. Sabisz, K. Lemke, A. Pieczykolan, M. Gałązka, K. Wiciejowska, J. Wietrzyk; Structural Factors Affecting Cytotoxic Activity of (E)-1-(Benzo[d ][1,3]oxathiol-6-yl)-3-phenylprop-2-en-1-one Derivatives; Chem. Biol. Drug Des. 84 (2014), 86-91. (go to article)
- J. Sączewski, A. Kędzia, A. Jalińska; New derivatives of 4,6-dimethylisoxazolo[3,4-b] pyridin-3(1H)-one: synthesis, tautomerism, electronic structure and antibacterial activity; Heterocycl. Commun. 51 (2014), 215-223. (go to article)
- J. Sączewski, M. Korcz; Synthesis and reactivity of heterocyclic hydroxylamine-O-sulfonates; Heterocycl. Commun. 51 (2014), 133-147.
(go to article) - H. Foks, D. Pancechowska-Ksepko, K. Gobis; Synthesis and Characterization of Novel N-Alkylamine- and N-Cycloalkylamine-Derived 2-Benzoyl-N-aminohydrazinecarbothioamides, 1,3,4-Thiadiazoles and 1,2,4-Triazole-5(4H)thiones; J. Het. Chem. 51 (2014), 98-105,
(go to article) - R. Hałasa, K. Turecka, Cz. Orlewska, W. Werel; Comparison of fluorescence optical respirometry and microbroth dilution methods for testing antimicrobial compounds; J. Microbiol. Methods. 107 (2014), 98-105.
(go to article) - E. Słomińska, T. Borkowski, I. Rybakowska, M. Abramowicz-Glinka, Cz. Orlewska, R. Smolenski; In Vitro and Cellular Effects of 4-Pyridone-3-Carboxamide Riboside on Enzymes of Nucleotide Metabolism; Nucleos. Nucleot. Nucleic Acids. 33 (2014), 353-357.
(go to article) - J. Sławiński, Z. Brzozowski , B. Żołnowska, K. Szafrański, A. Pogorzelska, D. Vullo, C.T. Suipuran; Synthesis of a new series of N4-substituted 4-(2-aminoethyl)benzenesulfonamides and their inhibitory effect on human carbonic anhydrase cytosolic isozymes I and II and transmembrane tumor-associated isozymes IX and XII Eur. J. Med. Chem. 84 (2014), 59-67 (go to full text)
- J. Sławiński, A. Pogorzelska, B. Żołnowska, K. Brożewicz, D. Vullo, C.T. Suipuran Carbonic anhydrase inhibitors. Synthesis of a novel series of 5-substituted 2,4-dichlorobenzenesulfonamides and their inhibition of human cytosolic isozymes i and II and the transmembrane tumor-associated isozymes IX and XII Eur. J. Med. Chem. 82 (2014), 47-55 (full version)
- Z. Brzozowski, J. Sławiński, K. Szafrański On the reactioj products of 4-substituted 3-pyridinesulfonamides with some benzenesulfonyl chloride derivatives J. Heterocyclic Chem. 51 (2014), 11-17 (przejdź do artykułu)
- A. bogdanowicz, H. Foks, K. Gobis, A. Kędzia, E. Kwapisz, A. Olczak, M.L. Główka; The Synthesis and Antibacterial Activity of Novel 4-Pyrrolidin-3-cyanopyridine Derivatives; J. Het. Chem. 50 (2013), 544-550
(go to article) - J. Saczewski, M. Korcz, P. Karczewska, M. Gdaniec; Reactivity of cyclic alkoxyguanidines – experimental and theoretical studies; Arkivoc, part IV (2013), 346-362.
(go to article) - M. Belka, J. Slawinski, L. Konieczna, P. Kawczak, T. Ciesielski, T. Baczek; Antitumor Activity of Novel Benzensulfonamide Derivatives in View of their Physiochemical Properties Searched by Principal Component Analysis; Med. Chem. 9 (2013), 517-525 (go to article)
- J. Sławiński, K. Szafrański, D. Vullo, C.T. Supuran, Carbonic anhydrase inhibitors. Synthesis of heterocyclic 4-substituted pyridine-3-sulfonamide derivativesband their inhibition of the human cytosolic isozymes I and II and transmembrane tumor-associated isozymes IX and XII, Eur. J. Med. Chem. 69, (2013), 701-710 (go to article)
- Z. Brzozowski, J. Sławiński, Synthesis of Novel Series of 6-Chloro-1,1-dioxo-1,4,2-benzodithiazine derivatives with potential biological activity, J. Heterocyclic Chem., 50, 5, (2013) 1099–1107(go to article)
- J. Sławiński, A. Pogorzelska, B. Żołnowska, T. Laskowski, P. Sowiński, Synthesis and structure determination of 2,3-diaryl-9,9-dioxo-1H-9-thia-1,4,4a,7,10-pentaazaphenanthrene-2-ols, Tetrahedron 69 (2013) 8675-8679 (go to article)
- K. Gobis, H. Foks, J. Sławiński, E. Augustynowicz-Kopeć, A Napiórkowska, Synthesis and biological activity of novel 3-heteroaryl-2H-pyrido[4,3-e][1,2,4]thiadiazine and 3-heteroaryl-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxides. Monatsh. Chem. 144, 8 (2013) 1197-1203 (go to article)
- Z. Brzozowski, B. Żołnowska, J. Sławiński, Synthesis of a new series of biologically interesting 6'-chloro-1',1'-dioxospiro[4H-benzo[d[1,3,7]oxadizocine-4,3'(2H)-[1,4,2]benzodithiazine-2,6(1H,5H)dione derivatives Monatsh. Chem. 144, 9 (2013) 1397-1405 (go to article)
- K. Gobis, H. Foks, J. Sławiński, A. Sikorski, D. Trzybiński, E. Augustynowicz-Kopeć, A Napiórkowska, K. Bojanowski, Synthesis, structure and biological activity of novel heterocyclic sulfonyl-carboximidamides. Monatsh. Chem. 144, 5 (2013) 647-658 (go to article)
- J. Sławiński, B. Żołnowska, D. Pirska, A. Kędzia, E. Kwapisz, Synthesis and antibacterial activity of novel 4-chloro-2-mercaptobenzenesulfonamide derivatives, J. Enzyme Inhib. Med. Chem. 28 (2013) 41-51 (go to article)
- J. Sławiński, B. Żołnowska, Cz. Orlewska, J. Chojnacki, Synthesis and molecular structure of novel 2-alkylthio-4-chloro-N -(5-oxo-4,5-dihydro-1H -1,2,4-triazolo-3-yl)-5-methylbenzenesulfonamides with potential anticancer activity Monatsh. Chem. 143, 12 (2012) 1705-1718 (go to article)
- Z. Brzozowski, J. Sławiński, D. Vullo, C.T. Supuran, Carbonic anhydrase inhibitors, regioselective synthesis of novel series 1-substituted 1,4-dihydro-4-oxo-3-pyridinesulfonamides and their inhibition of the human cytosolic isozymes I and II and transmembrane cancer associated isozymes IX and XII, Eur. J. Med. Chem. 56, (2012) 282-291
- K.Brożewicz, J. Sławiński, , 1-(2-Mercaptobenzenesulfonyl)-3-hydroxyguanidines – Novel potent antiproliferatives, synthesis and in vitro biological activity, Eur. J. Med. Chem . 55, (2012) 384-394
- K. Gobis, H. Foks, K. Wiśniewska, M. Dąbrowska-Szponar, E. Augustynowicz-Kopeć, A. Napiórkowska, Synthesis, and antimicrobal activity of novel heterocyclic sulfamoyl-phenyl-carboximidamides derived from clinically applied sulfonamides, Arch. Pharm. 345, 11 (2012) 911-917
- K. Gobis, H. Foks, K. Bojanowski E. Augustynowicz-Kopeć, A. Napiórkowska, Synthesis, of novel 3-cyclohexylpropanoic acid-derived nitrogen heterocyclic compounds and their evaluation for tuberculostatic activity. Bioorg. Med. Chem. 20, 1 (2012) 137-144
- K. Gobis, H. Foks, K. Wiśniewska, M. Dąbrowska-Szponar, E. Augustynowicz-Kopeć, A. Napiórkowska, A. Sikorski, Synthesis, structure, and antimicrobal activity of heterocyclic phenylsulfonyl- and 4-aminophenylsulfonyl-carboximidamides, Monatsh. Chem. 143, 8 (2012) 1161-1169
- K. Gobis, H. Foks, E. Augustynowicz-Kopeć, A. Napiórkowska, M. Szczesio, A. Olczak, M.L. Główka, Synthesis, characterization, and tuberculostatic activity of novel 2-(4-nitrobenzoyl)hydrazinecarbodithioic acid derivatives , Monatsh. Chem. 143, 4 (2012) 607-617
- K. Gobis, H. Foks, E. Augustynowicz-Kopeć, A. Napiórkowska; Synthesis and tuberculostatic activity of novel diverse heterocyclic compounds derived from heterocyclic carbohydrazides and methyl 2-heteroaroylhydrazinecarbodithioates, Heterocycles, 58, 4 (2012) 871–885
- K. Brożewicz, J. Sławiński, Synthesis and in vitro activity of novel 2-benzylthio-4-chloro-5-(1,3,4-oxadiazol-2-yl)benzenesulfonamide derivatives, Monatsh. Chem., 143, 6 (2012) 975-984
- Z. Brzozowski, J. Sławiński, M. Gdaniec, A. Innocenti, C.T. Supuran, Carbonic anhydrase inhibitors. Synthesis, molecular structures, and inhibition of the human cytosolic isozymes I and II and transmembrane isozymes IX, XII (cancer-associated) and XIV with novel 3-pyridinesulfonamide derivatives, Eur. J. Med. Chem., 46, 9 (2011) 4403–4410
- J. Sławiński, K. Brożewicz, A. Fruziński, M.L. Główka, Synthesis and antitumor activity of novel N'-(2-benzylthiobenzenesulfonyl)-1H-pyrazole-1-amidine derivatives, Heterocycles, 83, 5 (2011) 1093–1109
- Z. Brzozowski, J. Sławiński, A. Innocenti, C.T. Supuran, Carbonic anhydrase inhibitors, regioselective synthesis of novel 1-substituted 1,4-dihydro-4-oxo-3-pyridinesulfonamides and their inhibition of the human cytosolic isozymes I and II and transmembrane cancer associated isozymes IX and XII, Eur. J. Med. Chem., 45, 9 (2010) 3656–3661
- Z. Brzozowski, J. Sławiński, F. Sączewski, A. Innocenti, C.T. Supuran, Carbonic anhydrase inhibitors: Synthesis and inhibition of the human cytosolic isozymes I and II and transmembrane isozymes IX, XII (cancer-associated) and XIV with 4-substituted 3-pyridinesulfonamides, Eur. J. Med. Chem., 45, 6 (2010) 2396–2404
- Z. Brzozowski, J. Sławiński, Reaction products of activated aromatic and heteroaromatic chlorides with N,_N_-disubstituted formamides, Synth. Commun., 40 (2010) 1639–1645
- K. Gobis, H. Foks, Microwave-assisted synthesis of novel 4-N,N-dimethylamino- and 4-cycloamino- substituted 1,2,4-triazole-3-thiones, Heteroatom, 21, 3 (2010) 188–195
- B. Pilarski, A. Dobkowska, H. Foks, T. Michałowski, Modelling of acid-base equilibria in binary-solvent systems: a comparative study, Talanta, 80 (2010) 1073–1080
- Z. Brzozowski, J. Sławiński, A. Kędzia, E. Kwapisz, M. Gdaniec, Application of 3-methylthiopyrido[4,3-e]-1,4,2-dithiazine 1,1-dioxide to the synthesis of novel series of 4H-pyrido[4,3-e]-1,2,4-thiadiazine derivatives with potential biological activity, J. Heterocyclic Chem., 46, 6 (2009) 1396–1403
- Z. Brzozowski, F. Sączewski, J. Sławiński, T. Sanchez, N. Neamati, Synthesis and anti-HIV-1 integrase activities of 3-aroyl-2,3-dihydro-1,1-dioxo-1,4,2-benzodithiazines, Eur. J. Med. Chem., 44, 1 (2009) 190–196
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