Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Karolina Królewska-Golińska"'
Autor:
Marcin Cieślak, Mariola Napiórkowska, Julia Kaźmierczak-Barańska, Karolina Królewska-Golińska, Anna Hawrył, Iwona Wybrańska, Barbara Nawrot
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4318 (2021)
Based on previously identified dicarboximides with significant anticancer and immunomodulatory activities, a series of 26 new derivatives were designed and synthesized by the Diels–Alder reaction between appropriate diene and maleimide or hydroxyma
Externí odkaz:
https://doaj.org/article/1d7532d8de3d4321ad554ee1388a9d5e
Autor:
Angelika A. Adamus-Grabicka, Magdalena Markowicz-Piasecka, Marcin Cieślak, Karolina Królewska-Golińska, Paweł Hikisz, Joachim Kusz, Magdalena Małecka, Elzbieta Budzisz
Publikováno v:
Molecules, Vol 25, Iss 7, p 1613 (2020)
A series of 3-benzylidenechrmanones 1, 3, 5, 7, 9 and their spiropyrazoline analogues 2, 4, 6, 8, 10 were synthesized. X-ray analysis confirms that compounds 2 and 8 crystallize in a monoclinic system in P21/n space groups with one and three molecule
Externí odkaz:
https://doaj.org/article/0110b97906a9475e8c3219c4e2df286a
Autor:
Marcin Cieślak, Julia Kaźmierczak-Barańska, Karolina Królewska-Golińska, Mariola Napiórkowska, Iga Stukan, Urszula Wojda, Barbara Nawrot
Publikováno v:
Biomolecules, Vol 9, Iss 9, p 446 (2019)
We identified novel dicarboximides that were selectively cytotoxic towards human leukemia cells. Using chemical and biological methods, we characterized the biological activity, identified cellular protein targets and defined the mechanism of action
Externí odkaz:
https://doaj.org/article/fbc68bbab05b4cfc9d48c259115ea71c
Publikováno v:
Proceedings, Vol 22, Iss 1, p 62 (2019)
In continuation of synthetic pursuit of metallo-nucleosides, in particular dicobalt hexacarbonyl 5-alkynyl-2′-deoxyuridines, novel compounds with alkynyl groups were synthesized, starting from 5-iodo-2′-deoxyuridine. Reactions of dicobalt octacar
Externí odkaz:
https://doaj.org/article/d33bca8e92534ff3890e216dd22b3d96
Autor:
Dorota Krasowska, Nunzio Iraci, Claudio Santi, Józef Drabowicz, Marcin Cieslak, Julia Kaźmierczak-Barańska, Martina Palomba, Karolina Królewska-Golińska, Jakub Magiera, Luca Sancineto
Publikováno v:
Molecules, Vol 24, Iss 16, p 2914 (2019)
A series of variously functionalized selenium-containing compounds were purposely synthesized and evaluated against a panel of cancer cell lines. Most of the compounds showed an interesting cytotoxicity profile with compound 5 showing a potent activi
Externí odkaz:
https://doaj.org/article/539d20c995264d4ebc45dd888023c498
Autor:
Mariola Napiórkowska, Marcin Cieślak, Julia Kaźmierczak-Barańska, Karolina Królewska-Golińska, Barbara Nawrot
Publikováno v:
Molecules, Vol 24, Iss 8, p 1529 (2019)
The results of our previous research indicated that some derivatives of benzofurans, particularly halogeno-derivatives, are selectively toxic towards human leukemia cells. Continuing our work with this group of compounds we here report new data on th
Externí odkaz:
https://doaj.org/article/0f23eb1df3084dbea540081b273f67a3
Autor:
Iga, Stukan, Marek, Gryzik, Grażyna, Hoser, Andrew, Want, Wioleta, Grabowska-Pyrzewicz, Mikolaj, Zdioruk, Mariola, Napiórkowska, Marcin, Cieślak, Karolina, Królewska-Golińska, Barbara, Nawrot, Grzegorz, Basak, Urszula, Wojda
Publikováno v:
Cancers. 14(15)
The search is ongoing for new anticancer therapeutics that would overcome resistance to chemotherapy. This includes chronic myeloid leukemia, particularly suitable for the studies of novel anticancer compounds due to its homogenous and well-known gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::78fc6c3828b619f620058765a15f1739
https://pubmed.ncbi.nlm.nih.gov/35892900
https://pubmed.ncbi.nlm.nih.gov/35892900
Autor:
M. Richert, Karolina Królewska-Golińska, Marcin Cieślak, Julia Kaźmierczak-Barańska, Stanisław Biniak, Janusz W. Sobczak, Mariusz Walczyk, Grzegorz Trykowski
Publikováno v:
Dalton Transactions. 49:16791-16800
Functionalized carbon nanotubes are interesting, promising and unique delivery systems for anticancer drugs, which are now in the spotlight of nanomedicine. Connecting nanotubes with anticancer drugs or new compounds with anticancer properties aims a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1af42f5f22be75ee0ae1f09a7c92d1cd
https://doi.org/10.1039/d0dt03528a
https://doi.org/10.1039/d0dt03528a
Autor:
Tadeusz Muzioł, Julia Kaźmierczak-Barańska, Karolina Królewska-Golińska, Marcin Cieślak, Stanisław Biniak, Mariusz Walczyk, Renata Mikstacka, M. Richert
Publikováno v:
Processes; Volume 9; Issue 12; Pages: 2100
Processes, Vol 9, Iss 2100, p 2100 (2021)
Processes, Vol 9, Iss 2100, p 2100 (2021)
Gold(I) complexes with phosphine ligands—[Au(TrippyPhos)Cl] (1) (TrippyPhos = 1-[2-[bis(tert-butyl)phosphino]phenyl]-3,5-diphenyl-1H-pyrazole), [Au(BippyPhos)Cl]0.5CH2Cl2 (2) (BippyPhos = 5-(di-tert-butylphosphino)-1′, 3′, 5′-triphenyl-1′H-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dea33c9fe22cf9a1e17050da23917bb7
Autor:
Grzegorz Wrzeszcz, Tadeusz Muzioł, Stanisław Biniak, Mariusz Walczyk, Karolina Królewska-Golińska, M. Richert, Marcin Cieślak, Julia Kaźmierczak-Barańska
Publikováno v:
Dalton Transactions. 48:10689-10702
Two mononuclear ruthenium(iii) mer- and fac-isomers of the formula [RuCl3(PPh3)(dmpbt)] (where PPh3 = triphenylphosphine, dmpbt = 2-(3,5-dimethylpyrazoll-yl)benzothiazole) have been synthesised from the reaction of [RuCl3(PPh3)3] with a bidentate lig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe33dfc39ea0c617de64dfa00008c0b9
https://doi.org/10.1039/c9dt01803d
https://doi.org/10.1039/c9dt01803d