Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Šárka Mascaretti"'
Autor:
Jana Čurillová, Mária Pecháčová, Tereza Padrtová, Daniel Pecher, Šárka Mascaretti, Josef Jampílek, Ľudmila Pašková, František Bilka, Gustáv Kováč, Ivan Malík
Publikováno v:
Applied Sciences, Vol 12, Iss 1, p 300 (2021)
This research focused on a three-step synthesis, analytical, physicochemical, and biological evaluation of hybrid molecules 6a–g, containing a lipophilic 3-trifluoromethylphenyl moiety, polar carbamoyloxy bridge, 2-hydroxypropan-1,3-diyl chain and
Externí odkaz:
https://doaj.org/article/3b7a2e01565f4fd98f8600142b84c427
Autor:
Eva Havránková, Vladimír Garaj, Šárka Mascaretti, Andrea Angeli, Zuzana Soldánová, Miroslav Kemka, Jozef Motyčka, Marie Brázdová, Jozef Csöllei, Josef Jampílek, Claudiu T. Supuran
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 1, p 231 (2021)
A series of 1,3,5-triazinyl aminobenzenesulfonamides substituted by aminoalcohol, aminostilbene, and aminochalcone structural motifs was synthesized as potential human carbonic anhydrase (hCA) inhibitors. The compounds were evaluated on their inhibit
Externí odkaz:
https://doaj.org/article/b5e2c1473ecf40f9ac258763a34d8457
Publikováno v:
Antioxidants, Vol 10, Iss 8, p 1288 (2021)
Nature has been a source of inspiration for the development of new pharmaceutically active agents. A series of new unnatural gallotannins (GTs), derived from d-lyxose, d-ribose, l-rhamnose, d-mannose, and d-fructose have been designed and synthesized
Externí odkaz:
https://doaj.org/article/2730f808e6ec4d869d5097fc93f2f807
Autor:
Eva Havránková, Vladimír Garaj, Šárka Mascaretti, Andrea Angeli, Zuzana Soldánová, Miroslav Kemka, Jozef Motyčka, Marie Brázdová, Jozef Csöllei, Josef Jampílek, Claudiu T. Supuran
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 231, p 231 (2022)
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 231
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 231
A series of 1,3,5-triazinyl aminobenzenesulfonamides substituted by aminoalcohol, aminostilbene, and aminochalcone structural motifs was synthesized as potential human carbonic anhydrase (hCA) inhibitors. The compounds were evaluated on their inhibit
Autor:
Dominika Pindjakova, Sarka Mascaretti, Jana Hricoviniova, Jan Hosek, Jana Gregorova, Jiri Kos, Alois Cizek, Zuzana Hricoviniova, Josef Jampilek
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e29051- (2024)
A series of nine 2,3-disubstituted-quinazolin-4(3H)-one derived Schiff bases and their three Cu(II) complexes was prepared and tested for their antimicrobial activities against reference strains Staphylococcus aureus ATCC 29213 and Enterococcus faeca
Externí odkaz:
https://doaj.org/article/c93bbeea697947a7bae249ccc816211c