Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Miroslava Martinková"'
Autor:
Natália Nosálová, Alexandra Kešeľáková, Martin Kello, Miroslava Martinková, Dominika Fábianová, Martina Bago Pilátová
Background A series of experiments on colorectal cancer cells (Caco-2 and HCT116) were conducted to provide new information about the antiproliferative and pro-apoptotic effect of newly synthesized (2S,3S,4R)-2-Tridecylpyrrolidine-3,4-diol hydrochlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddd10259d6f3c30122537c2937e78aea
https://doi.org/10.21203/rs.3.rs-2915671/v1
https://doi.org/10.21203/rs.3.rs-2915671/v1
Autor:
Simona Fazekašová, Jozef Gonda, Miroslava Martinková, Martina Bago Pilátová, Monika Majirská, Veronika Turčanová, Dávid Jáger
Publikováno v:
Tetrahedron. 137:133391
Autor:
Kristína Vargová, Miroslava Martinková, Jana Špaková Raschmanová, Martina Bago Pilátová, Alexandra Kešeľáková, Dávid Jáger
Publikováno v:
Carbohydrate Research. 526:108789
Autor:
Miroslava Martinková, Jozef Gonda, Tatiana Mitríková, Simona Fazekašová, Dávid Roman, Martina Pilátová
Publikováno v:
Organic & Biomolecular Chemistry. 17:3361-3373
A flexible synthetic approach towards biologically active sphingoid base-like compounds with an integrated azobenzene framework was achieved via installing a chiral amino-alcohol fragment into the azobenzene system by utilizing the Wittig olefination
Autor:
Sergej Šesták, Martina Pilátová, Michael Široký, Miroslava Martinková, Mária Vilková, Samuel Homolya, Jozef Gonda
Publikováno v:
Tetrahedron. 75:398-408
A straightforward stereoselective route towards (3aR,5R,6S,7R,7aR)- and (3aR,5R,6S,7R,7aR)-octahydro-1H-indole-5,6,7-triol, analogues of castanospermine, starting from the corresponding shikimic acid derivatives is described. The key transformations
Autor:
Miroslava Martinková, Miroslava Čonková, Jozef Gonda, Martina Pilátová, Daniel Kupka, Dominika Jacková, Dávid Jáger
Publikováno v:
Carbohydrate Research. 472:76-85
A flexible synthetic approach to biologically active sphingoid base-like compounds with a 3-amino-1,2-diol framework was achieved through a [3,3]-sigmatropic rearrangement and late stage olefin cross-metathesis as the key transformations. The stereoc
Autor:
Tatiana Pončáková, Martin Fábian, Miroslava Martinková, Michaela Novotná, Milica Fabišíková, Monika Tvrdoňová, Martina Bago Pilátová, Natália Nosálová, Juraj Kuchár, Dávid Jáger, Miroslava Litecká
Publikováno v:
Tetrahedron. 121:132910
Autor:
Martina Pilátová, Eva Mezeiová, Peter Petik, Petr Gál, Alexandra Bogdanova, Miroslava Martinková, Ladislav Mirossay, Martin Kello, Alexandra Macejova, Natalia Nosalova, Peter Takáč
Publikováno v:
Anticancer research. 41(6)
Background/aim A series of experiments on HeLa cells were conducted to provide new information concerning the anti-cancer properties of jaspine B hydrochloride (JBH). Materials and methods HeLa cells treated with 0.5 μmol/l JBH for 24, 48, and 72 h
Autor:
Martina Pilátová, Miroslava Martinková, Jana Špaková Raschmanová, Miroslava Litecká, Michaela Novotná, Dávid Jáger, Juraj Kuchár
Publikováno v:
Tetrahedron. 103:132570
A successful strategy for the construction of novel isomeric aza-analogues 13. HCl and 14. HCl of natural jaspine B was developed by constructing a vicinal diamino motif via a sequential Overman rearrangement, followed by a pyrrolidine core formation
Autor:
Martina Pilátová, Dominika Jacková, Milica Fabišíková, Jozef Gonda, Juraj Kuchár, Miroslava Martinková
Publikováno v:
Carbohydrate Research. 468:51-63
Two approaches to a small library of cytotoxic dihydrosphingosine analogues are described. [3,3]-Sigmatropic rearrangements along with an OCM reaction were used as the key steps for the construction of the two isodihydrosphingosines ent-6 and 10, whe