Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Paulina Strzyga-Łach"'
Autor:
Emilia Martula, Beata Morak-Młodawska, Małgorzata Jeleń, Paulina Strzyga-Łach, Marta Struga, Katarzyna Żurawska, Anna Kasprzycka, Weronika Bagrowska
Publikováno v:
Applied Sciences, Vol 14, Iss 16, p 7263 (2024)
Dimers of dipyridothiazines with an m-xylene moiety are presented in terms of a comparative analysis with anticancer active structural analogs containing a lutidine system. The synthesis of new isomeric dimers was described, the structure of which wa
Externí odkaz:
https://doaj.org/article/fee74264e36a48d4bcf5eddf2089f070
Autor:
Katarzyna Dziduch, Sara Janowska, Sylwia Andrzejczuk, Paulina Strzyga-Łach, Marta Struga, Marcin Feldo, Oleg Demchuk, Monika Wujec
Publikováno v:
Molecules, Vol 29, Iss 13, p 3023 (2024)
Heterocyclic compounds, particularly those containing azole rings, have shown extensive biological activity, including anticancer, antibacterial, and antifungal properties. Among these, the imidazole ring stands out due to its diverse therapeutic pot
Externí odkaz:
https://doaj.org/article/0404effa6aa048feb4f7ef19058cf88d
Autor:
Sara Janowska, Dmytro Khylyuk, Michał Janowski, Urszula Kosikowska, Paulina Strzyga-Łach, Marta Struga, Monika Wujec
Publikováno v:
Molecules, Vol 28, Iss 6, p 2718 (2023)
The treatment of infectious diseases is a challenging issue faced by the medical community. The emergence of drug-resistant strains of bacteria and fungi is a major concern. Researchers and medical professionals are working to develop new and innovat
Externí odkaz:
https://doaj.org/article/fbf79734c0b7426b8475768d22fda31f
Autor:
Grażyna Kubiak-Tomaszewska, Piotr Roszkowski, Emilia Grosicka-Maciąg, Paulina Strzyga-Łach, Marta Struga
Publikováno v:
Molecules, Vol 27, Iss 2, p 420 (2022)
Flavonoids and polyunsaturated fatty acids due to low cytotoxicity in vitro studies are suggested as potential substances in the prevention of diseases associated with oxidative stress. We examined novel 6-hydroxy-flavanone and 7-hydroxy-flavone conj
Externí odkaz:
https://doaj.org/article/55cfd283eeed452ebbcca117c1af0197
Publikováno v:
Pharmaceuticals, Vol 14, Iss 11, p 1097 (2021)
Substituted thiourea derivatives possess confirmed cytotoxic activity towards cancer but also normal cells. To develop new selective antitumor agents, a series of 3-(trifluoromethyl)phenylthiourea analogs were synthesized, and their cytotoxicity was
Externí odkaz:
https://doaj.org/article/c7197d877528405aa0fda44bf124f5f6
Autor:
Anna Bielenica, Giuseppina Sanna, Silvia Madeddu, Gabriele Giliberti, Joanna Stefańska, Anna E. Kozioł, Oleksandra Savchenko, Paulina Strzyga-Łach, Alicja Chrzanowska, Grażyna Kubiak-Tomaszewska, Marta Struga
Publikováno v:
Molecules, Vol 23, Iss 10, p 2428 (2018)
4-Chloro-3-nitrophenylthioureas 1–30 were synthesized and tested for their antimicrobial and cytotoxic activities. Compounds exhibited high to moderate antistaphylococcal activity against both standard and clinical strains (MIC values 2–64 μg/mL
Externí odkaz:
https://doaj.org/article/6a5e4fdbc088440281608bfbd13f9a5b
Publikováno v:
Pharmaceuticals
Volume 14
Issue 11
Pharmaceuticals, Vol 14, Iss 1097, p 1097 (2021)
Volume 14
Issue 11
Pharmaceuticals, Vol 14, Iss 1097, p 1097 (2021)
Substituted thiourea derivatives possess confirmed cytotoxic activity towards cancer but also normal cells. To develop new selective antitumor agents, a series of 3-(trifluoromethyl)phenylthiourea analogs were synthesized, and their cytotoxicity was
Autor:
Paulina, Strzyga-Łach, Hanna, Czeczot
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 40(236)
Chronic inflammation in the body leads to the formation and development many diseases, e.g. atherosclerosis, diabetes, neurodegenerative diseases or cancer and others. Therefore, the search for new and safe compounds of plant origin having antiinflam
Autor:
Paulina Strzyga-Łach, Czeczot, H.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6aaea459fdf252f1f5dfcc88a7f6976a
http://www.scopus.com/inward/record.url?eid=2-s2.0-84973409994&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84973409994&partnerID=MN8TOARS