Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Eva Havránková"'
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:
Molecules, Vol 25, Iss 9, p 2168 (2020)
We reported a novel simplified synthetic procedure for the preparation of monosubstituted piperazine derivatives which can now be easily prepared in a one-pot-one-step way from a protonated piperazine with no need of introduction of a protecting grou
Externí odkaz:
https://doaj.org/article/7e79032224ba4af7848f6dd6d847bf3f
Autor:
Eva Havránková, Nikola Čalkovská, Tereza Padrtová, Jozef Csöllei, Radka Opatřilová, Pavel Pazdera
Publikováno v:
Molecules, Vol 25, Iss 8, p 1787 (2020)
A series of 1,3,5-triazine analogues, incorporating aminobenzene sulfonamide, aminoalcohol/phenol, piperazine, chalcone, or stilbene structural motifs, were evaluated as potential antioxidants. The compounds were prepared by using step-by-step nucleo
Externí odkaz:
https://doaj.org/article/c764328cea0a4b9689ac75b2b3ca9ed3
Publikováno v:
Molecules, Vol 24, Iss 19, p 3586 (2019)
An efficient and simple methodology for Ullmann Cu(I)-catalyzed synthesis of di- and trisubstituted 1,3,5-triazine derivatives from dichlorotriazinyl benzenesulfonamide and corresponding nucleophiles is reported. Cations Cu(I) supported on macroporou
Externí odkaz:
https://doaj.org/article/79789a06215f4dee9e0ec8cbe6e7dca8
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
Publikováno v:
Bioorganic chemistry. 107
Simple molecular descriptors of extensive series of 1,3,5-triazinyl sulfonamide derivatives, based on the structure of sulfonamides and their physicochemical properties, were designed and calculated. These descriptors were successfully applied as inp
Publikováno v:
Molecules
Volume 25
Issue 9
Molecules, Vol 25, Iss 2168, p 2168 (2020)
Volume 25
Issue 9
Molecules, Vol 25, Iss 2168, p 2168 (2020)
We reported a novel simplified synthetic procedure for the preparation of monosubstituted piperazine derivatives which can now be easily prepared in a one-pot-one-step way from a protonated piperazine with no need of introduction of a protecting grou
Autor:
Pavel Pazdera, Nikola Čalkovská, Tereza Padrtova, Radka Opatřilová, Eva Havránková, Jozef Csöllei
Publikováno v:
Molecules
Volume 25
Issue 8
Molecules, Vol 25, Iss 1787, p 1787 (2020)
Volume 25
Issue 8
Molecules, Vol 25, Iss 1787, p 1787 (2020)
A series of 1,3,5-triazine analogues, incorporating aminobenzene sulfonamide, aminoalcohol/phenol, piperazine, chalcone, or stilbene structural motifs, were evaluated as potential antioxidants. The compounds were prepared by using step-by-step nucleo
Publikováno v:
Proceedings of The 23rd International Electronic Conference on Synthetic Organic Chemistry.
We report a novel sophisticated synthetic method for preparation of monosubstituted piperazine derivatives, which can now be easily prepared in a one-pot-one-step way from a free piperazine with no need of introduction of a protecting group bringing
Autor:
Tereza Padrtova, Pavel Pazdera, Nikola Čalkovská, Jozef Csöllei, Eva Havránková, Radka Opatřilová
Publikováno v:
The 23rd International Electronic Conference on Synthetic Organic Chemistry.
A series of 1,3,5-triazine derivatives, incorporating aminobenzenesulfonamide, aminoalcohol/phenol, piperazine, chalcone, or stilbene structural motifs, were evaluated as potential antioxidants. The compounds were prepared by using step by step nucle