Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Eszter, Kalydi"'
Publikováno v:
Molecules, Vol 29, Iss 4, p 876 (2024)
The characteristic alkaloid component of the leaves of the catnip shrub (Catha edulis) is cathinone, and its synthetic analogs form a major group of recreational drugs. Cathinone derivatives are chiral compounds. In the literature, several chiral met
Externí odkaz:
https://doaj.org/article/dfe7b13ce3544242bc4f79d0421353c8
Publikováno v:
Molecules, Vol 26, Iss 17, p 5271 (2021)
In order to better understand the chiral recognition mechanisms of positively charged cyclodextrin (CD) derivatives, the synthesis, the pKa determination by 1H nuclear magnetic resonance (NMR)-pH titration and a comparative chiral capillary electroph
Externí odkaz:
https://doaj.org/article/6741a5203120440082082559c0791c09
Publikováno v:
Chemistry – A European Journal. 29
With the aim of developing green synthetic protocols for the photooxygenation of hydrophobic molecules in water, a combination of supramolecular and photo-chemistries was exploited. The photochemical synthesis of aromatic endoperoxides is a very well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04dc97b38c4090e33c38a90c6374d1ca
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 22; Pages: 14448
Acid-base properties of cyclodextrins (CDs), persubstituted at C-6 by 3-mercaptopropionic acid, sualphadex (Suα-CD), subetadex (Suβ-CD) and sugammadex (Suγ-CD, the antidote of neuromuscular blocking steroids) were studied by 1H NMR-pH titrations.
Autor:
Marco, Agnes, Mazza Arianna, Eszter, Kalydi, Beni, Szabolcs, Francesco, Manoli, Milo, Malanga, Julia, Manet Ilse Gert
Cyclodextrin (CyD)-polymers have been demonstrated to improve the water solubility and stability of conventional hydrophobic drugs and to be able to load in a single, biocompatible platform multiple therapeutic agents for cancer treatment. Photodynam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fc643458917e6836221929fb5211d4b
Sugammadex Analogue Cyclodextrins as Chiral Selectors for Enantioseparation of Cathinone Derivatives
Autor:
Dóra Ujj, Eszter Kalydi, Erzsébet Varga, Milo Malanga, Szabolcs Béni, Tamás Sohajda, Gabor Benkovics
Publikováno v:
SSRN Electronic Journal.
Autor:
Dóra Ujj, Eszter Kalydi, Milo Malanga, Erzsébet Varga, Tamás Sohajda, Szabolcs Béni, Gábor Benkovics
Publikováno v:
Journal of Chromatography A. 1683:463506
The present contribution describes the application of three single-isomeric cyclodextrin derivatives for the first time - Sugammadex, Subetadex and Sualphadex as chiral selectors. Their recognition ability was investigated by means of chiral capillar
Publikováno v:
Molecules, Vol 26, Iss 5271, p 5271 (2021)
Molecules
Volume 26
Issue 17
Molecules
Volume 26
Issue 17
In order to better understand the chiral recognition mechanisms of positively charged cyclodextrin (CD) derivatives, the synthesis, the pKa determination by 1H nuclear magnetic resonance (NMR)-pH titration and a comparative chiral capillary electroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c32cdc097103857921fc51a3c4f32329
http://hdl.handle.net/11562/1070217
http://hdl.handle.net/11562/1070217
Autor:
Sara Payamifar, Petr Kasal, Aurore Fraix, Fabiana Quaglia, Ovidio Catanzano, Salvatore Sortino, Eszter Kalydi, Mimimorena Seggio, Claudia Conte
This contribution reports the design, synthesis, photochemical properties and drug inclusion capability of two novel β-cyclodextrin (βCD) conjugates, βCD-NBFNO1 and βCD-NBFNO2, covalently integrating an N-nitroso amino-nitro-benzofurazan in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ef1c8abb61009cc2b2da96666c8376c
https://hdl.handle.net/11588/920951
https://hdl.handle.net/11588/920951