Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Beata, Żołnowska"'
Autor:
Katarzyna Górska, Marta Maskey-Warzęchowska, Małgorzata Barnaś, Adam Białas, Adam Barczyk, Hanna Jagielska-Len, Ewa Jassem, Aleksander Kania, Katarzyna Lewandowska, Sebastian Majewski, Magdalena M. Martusewicz-Boros, Wojciech J. Piotrowski, Alicja Siemińska, Krzysztof Sładek, Małgorzata Sobiecka, Marzena Trzaska-Sobczak, Witold Tomkowski, Beata Żołnowska, Rafał Krenke
Publikováno v:
Therapeutic Advances in Chronic Disease, Vol 13 (2022)
Background: Pirfenidone and nintedanib are considered as the standard of care in idiopathic pulmonary fibrosis (IPF), but there is no consensus as to which of these two agents should be regarded as first-line treatment. Objective: To provide real-wor
Externí odkaz:
https://doaj.org/article/f292078d43f34b2ea0136d89cf7f4dc6
Autor:
Sebastian Majewski, Adam J. Białas, Małgorzata Buchczyk, Paweł Gomółka, Katarzyna Górska, Hanna Jagielska-Len, Agnieszka Jarzemska, Ewa Jassem, Dariusz Jastrzębski, Aleksander Kania, Marek Koprowski, Rafał Krenke, Jan Kuś, Katarzyna Lewandowska, Magdalena M. Martusewicz-Boros, Kazimierz Roszkowski-Śliż, Alicja Siemińska, Krzysztof Sładek, Małgorzata Sobiecka, Karolina Szewczyk, Małgorzata Tomczak, Witold Tomkowski, Elżbieta Wiatr, Dariusz Ziora, Beata Żołnowska, Wojciech J. Piotrowski
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-12 (2020)
Abstract Background Pirfenidone is an antifibrotic agent approved for the treatment of idiopathic pulmonary fibrosis (IPF). The drug is available for Polish patients with IPF since 2017. The PolExPIR study aimed to describe the real-world data (RWD)
Externí odkaz:
https://doaj.org/article/819a0c653b2745e99c064475c66a7334
Publikováno v:
Medical Sciences Forum, Vol 14, Iss 1, p 42 (2022)
Cancer is a disease that has spread widely throughout the world and requires the development of new anticancer drugs. Curing cancer is a complicated process as the drugs that are used target human cells and cells that have undergone genetic changes a
Externí odkaz:
https://doaj.org/article/797ab774a15c4b4aab9fe21960caa007
Autor:
Monika Pastewska, Beata Żołnowska, Strahinja Kovačević, Hanna Kapica, Maciej Gromelski, Filip Stoliński, Jarosław Sławiński, Wiesław Sawicki, Krzesimir Ciura
Publikováno v:
Molecules, Vol 27, Iss 13, p 3965 (2022)
Sulfonamides are a classic group of chemotherapeutic drugs with a broad spectrum of pharmacological action, including anticancer activity. In this work, reversed-phase high-performance liquid chromatography and biomimetic chromatography were applied
Externí odkaz:
https://doaj.org/article/e80ded7d0fcf4212a75d42b975af059c
Autor:
Petar Žuvela, J. Jay Liu, Myunggi Yi, Paweł P. Pomastowski, Gulyaim Sagandykova, Mariusz Belka, Jonathan David, Tomasz Bączek, Krzysztof Szafrański, Beata Żołnowska, Jarosław Sławiński, Claudiu T. Supuran, Ming Wah Wong, Bogusław Buszewski
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 1430-1443 (2018)
In this work, a target-based drug screening method is proposed exploiting the synergy effect of ligand-based and structure-based computer-assisted drug design. The new method provides great flexibility in drug design and drug candidates with consider
Externí odkaz:
https://doaj.org/article/10af111bcd05473b8f60c43ce8cbd7a1
Autor:
Kawiak, Beata Żołnowska, Jarosław Sławiński, Mariusz Belka, Tomasz Bączek, Jarosław Chojnacki, Anna
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 11; Pages: 9768
A series of novel 2-alkythio-4-chloro-N-[imino-(heteroaryl)methyl]benzenesulfonamide derivatives, 8–24, were synthesized in the reaction of the N-(benzenesulfonyl)cyanamide potassium salts 1–7 with the appropriate mercaptoheterocycles. All the sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::fe018555dc2543ca9907c1cda88442ef
Autor:
Beata Żołnowska, Jarosław Sławiński, Mariusz Belka, Tomasz Bączek, Anna Kawiak, Jarosław Chojnacki, Aneta Pogorzelska, Krzysztof Szafrański
Publikováno v:
Molecules, Vol 20, Iss 10, Pp 19101-19129 (2015)
A series of novel N-acyl-4-chloro-5-methyl-2-(R1-methylthio)benzenesulfonamides 18–47 have been synthesized by the reaction of N-[4-chloro-5-methyl-2-(R1-methylthio) benzenesulfonyl]cyanamide potassium salts with appropriate carboxylic acids. Some
Externí odkaz:
https://doaj.org/article/cfa356af1eb141edbe3ed4a952c6af57
Autor:
Jarosław Sławiński, Beata Żołnowska, Zdzisław Brzozowski, Anna Kawiak, Mariusz Belka, Tomasz Bączek
Publikováno v:
Molecules, Vol 20, Iss 4, Pp 5754-5770 (2015)
A series of new 6-chloro-3-(2-arylmethylene-1-methylhydrazino)-1,4,2-benzodithiazine 1,1-dioxide derivatives were effectively synthesized from N-methyl-N-(6-chloro-1,1-dioxo-1,4,2-benzodithiazin-3-yl)hydrazines. The intermediate compounds as well as
Externí odkaz:
https://doaj.org/article/58de604fa7484b7eb2293c6d839840c7
Autor:
Jarosław Sławiński, Aneta Pogorzelska, Beata Żołnowska, Anna Kędzia, Marta Ziółkowska-Klinkosz, Ewa Kwapisz
Publikováno v:
Molecules, Vol 19, Iss 9, Pp 13704-13723 (2014)
Pathogenic fungi are one of the main causes of hospital-related infections. Since conventional antifungals have become less effective because of the increasing fungal resistance to the standard drugs, the need for new agents is becoming urgent. Herei
Externí odkaz:
https://doaj.org/article/1da3e5b9da6e49e794086010bfd35b1b
Autor:
Łukasz, Tomorowicz, Beata, Żołnowska, Krzysztof, Szafrański, Jarosław, Chojnacki, Ryszard, Konopiński, Ewa A, Grzybowska, Jarosław, Sławiński, Anna, Kawiak
Publikováno v:
International journal of molecular sciences. 23(13)
In the search for new compounds with antitumor activity, new potential anticancer agents were designed as molecular hybrids containing the structures of a triazine ring and a sulfonamide fragment. Applying the synthesis in solution, a base of new sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::528aab1240d9a0c9efdbef12135eabba
https://pubmed.ncbi.nlm.nih.gov/35806186
https://pubmed.ncbi.nlm.nih.gov/35806186