Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Marta Denel‐Bobrowska"'
Autor:
Magdalena Kowalewicz-Kulbat, Krzysztof T. Krawczyk, Izabela Szulc-Kielbik, Sebastian Rykowski, Marta Denel-Bobrowska, Agnieszka B. Olejniczak, Camille Locht, Magdalena Klink
Publikováno v:
Microbial Cell Factories, Vol 22, Iss 1, Pp 1-10 (2023)
Abstract Background Ovarian cancer is one of the most frequent and deadly gynaecological cancers, often resistant to platinum-based chemotherapy, the current standard of care. Halophilic microorganisms have been shown to produce a large variety of me
Externí odkaz:
https://doaj.org/article/41e508dc2a9341a78131de936959a070
Autor:
Carla Sardo, Giulia Auriemma, Carmela Mazzacano, Claudia Conte, Virgilio Piccolo, Tania Ciaglia, Marta Denel-Bobrowska, Agnieszka B. Olejniczak, Donatella Fiore, Maria Chiara Proto, Patrizia Gazzerro, Rita Patrizia Aquino
Publikováno v:
Pharmaceutics, Vol 16, Iss 8, p 971 (2024)
In this study, the structural attributes of nanoparticles obtained by a renewable and non-immunogenic “inulinated” analog of the “pegylated” PLA (PEG-PLA) were examined, together with the potential of these novel nanocarriers in delivering po
Externí odkaz:
https://doaj.org/article/1cc66af718814ce99ed1f1a5c0df29af
Autor:
Sebastian Rykowski, Dorota Gurda-Woźna, Agnieszka Fedoruk-Wyszomirska, Marta Orlicka-Płocka, Aleksandra Kowalczyk, Paweł Stączek, Marta Denel-Bobrowska, Katarzyna Biniek-Antosiak, Wojciech Rypniewski, Eliza Wyszko, Agnieszka B. Olejniczak
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 38, Iss 1 (2023)
The synthesis of carborane-1,8-naphthalimide conjugates and evaluation of their DNA-binding ability and anticancer activity were performed. A series of 4-carboranyl-3-nitro-1,8-naphthalimide derivatives, mitonafide and pinafide analogs, were synthesi
Externí odkaz:
https://doaj.org/article/da14e44f868943c69fa7db724c26232b
Autor:
Grzegorz Mlostoń, Mateusz Kowalczyk, Małgorzata Celeda, Marcin Jasiński, Marta Denel-Bobrowska, Agnieszka B. Olejniczak
Publikováno v:
Molecules, Vol 27, Iss 11, p 3524 (2022)
Starting with fluorinated benzylamines, a series of 2-unsubstituted imidazole N-oxides was prepared and subsequently deoxygenated in order to prepare the corresponding imidazoles. The latter were treated with benzyl halides yielding imidazolium salts
Externí odkaz:
https://doaj.org/article/f70b7cc0dfe3487db15412bddaab23dd
Autor:
Daria Różycka, Aleksandra Kowalczyk, Marta Denel‐Bobrowska, Olga Kuźmycz, Magdalena Gapińska, Paweł Stączek, Agnieszka B. Olejniczak
Publikováno v:
ChemMedChem. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6eefa5d42150682ea6400ab43505f46
https://doi.org/10.1002/cmdc.202200666
https://doi.org/10.1002/cmdc.202200666
Autor:
Agnieszka B. Olejniczak, Marzena Dzida, Edward Zorębski, Marta Denel-Bobrowska, Małgorzata Musiał
Publikováno v:
ACS Sustainable Chemistry & Engineering. 9:16459-16465
In the current work, we present a broad analysis of cytotoxicity toward normal (kidney and lung) and cancer (lung, liver, and cervix) cells of ionic liquids (ILs) with imidazolium cations and cyano-based or bis(trifluoromethylsulfonyl)imide anions. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761243e6eb69c04ba99c936327106934
https://doi.org/10.1021/acssuschemeng.1c06580
https://doi.org/10.1021/acssuschemeng.1c06580
Autor:
Franz Steppeler, Dominika Iwan, Radosław Gaida, Marta Denel-Bobrowska, Agnieszka B. Olejniczak, Elżbieta Wojaczyńska
Publikováno v:
Biomedicine & Pharmacotherapy. 164:114908
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f304646351bfbce087900bb24ec80c9
https://doi.org/10.1016/j.biopha.2023.114908
https://doi.org/10.1016/j.biopha.2023.114908
Autor:
Dominika Iwan, Karolina Kamińska, Marta Denel-Bobrowska, Agnieszka B. Olejniczak, Elżbieta Wojaczyńska
Publikováno v:
Biomedicinepharmacotherapy = Biomedecinepharmacotherapie. 153
Chiral sulfonamides with aromatic fragments are important chemical building blocks found widely in many natural products, catalysts, and molecules of biological importance. In this report, we describe the efficient synthesis of a series of chiral sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1960fe47f8f3997ca2ecb6bfe81c4fad
https://pubmed.ncbi.nlm.nih.gov/36076578
https://pubmed.ncbi.nlm.nih.gov/36076578
Publikováno v:
European Journal of Medicinal Chemistry
Nucleosides and their derivatives are a well-known and well-described class of compounds with antiviral activity. Currently, in the era of the COVID-19 pandemic, scientists are also looking for compounds not related to nucleosides with antiviral prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a68e1058951e3eb81b079fe2bc4f1a62
http://europepmc.org/articles/PMC8769541
http://europepmc.org/articles/PMC8769541
Publikováno v:
Life Sciences. 178:1-8
Doxorubicin (DOX) is one of the most commonly used and effective chemotherapeutic agents. Despite its clinical benefits, the use of DOX is often limited by serious adverse effects, such as severe cardiotoxicity and myelosuppression. Recent progress i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f397ff8adefa0c2632a27d557337bab
https://doi.org/10.1016/j.lfs.2017.04.009
https://doi.org/10.1016/j.lfs.2017.04.009