Agata J Pacula
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Explore the profile of Agata J Pacula including associated specialties, affiliations and a list of published articles.
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6
Citations
47
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Recent Articles
1.
Obieziurska-Fabisiak M, Pacula A, Capoccia L, Drogosz-Stachowicz J, Janecka A, Santi C, et al.
Molecules
. 2020 Jul;
25(15).
PMID: 32722043
The ability of organoselenium molecules to mimic the activity of the antioxidant selenoenzyme glutathione peroxidase (GPx) allows for their use as antioxidant or prooxidant modulators in several diseases associated with...
2.
Obieziurska M, Pacula A, Laskowska A, Dlugosz-Pokorska A, Janecka A, Scianowski J
Materials (Basel)
. 2020 Feb;
13(3).
PMID: 32024274
Organoselenium compounds are well-known glutathione peroxidase (GPx) mimetics that possess antioxidants/prooxidant properties and are able to modulate the concentration of reactive oxygen species (ROS), preventing oxidative stress in normal cells...
3.
Obieziurska M, Pacula A, Dlugosz-Pokorska A, Krzeminski M, Janecka A, Scianowski J
Materials (Basel)
. 2019 Nov;
12(21).
PMID: 31683558
A series of new chiral benzisoselenazol-3(2H)-ones substituted on the nitrogen atom with three monoterpene moieties--menthane, pinane and carane-was synthesized. The compounds were obtained by the reaction of 2-(chloroseleno)benzoyl chloride with...
4.
Scianowski J, Pacula A, Skowronek P
Chirality
. 2017 Aug;
29(10):599-602.
PMID: 28771847
The twisted structure of ditellurides, in a similar way as in other dichalcogenes, leads to different absorption of circularly polarized light by quasi-enantiomeric chiral orbitals. Chiral optically active ditellurides are...
5.
Pacula A, Kaczor K, Antosiewicz J, Janecka A, Dlugosz A, Janecki T, et al.
Molecules
. 2017 Mar;
22(3).
PMID: 28335518
New chiral camphane-derived benzisoselenazol-3(2H)-ones and corresponding diselenides have been synthetized using a convenient one-pot procedure. Se-N bond was efficiently converted to an Se-Se bond, which could also be easily re-oxidized...
6.
Pacula A, Kaczor K, Wojtowicz A, Antosiewicz J, Janecka A, Dlugosz A, et al.
Bioorg Med Chem
. 2016 Dec;
25(1):126-131.
PMID: 28029457
A series of N-alkyl benzisoselenazol-3(2H)-ones has been obtained and transformed to corresponding diselenides by the reduction with sodium borohydride. Additionally, efficient methodology for the oxidative Se-N bond formation by potassium...