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Draginja Mrvoš-Sermek

Researcher at University of Zagreb

Publications -  35
Citations -  266

Draginja Mrvoš-Sermek is an academic researcher from University of Zagreb. The author has contributed to research in topics: Hydrogen bond & Crystal structure. The author has an hindex of 9, co-authored 34 publications receiving 249 citations.

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Synthesis, crystal structure and antiproliferative evaluation of some new substituted benzothiazoles and styrylbenzothiazoles.

TL;DR: The multistep synthesis of a series of new substituted-benzothiazoles as hydrochloride or quaternary salts exerted a different inhibitory effect, depended on concentration and type of the cells.
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Synthesis, structural studies, and cytostatic evaluation of 5,6-di-O-modified l-ascorbic acid derivatives

TL;DR: 6-Chloro derivative of 2,3-di-O-benzyl-5, 6-epoxy- and 5,6-isopropylidene-l-ascorbic acid showed the best cytostatic effects against all tested malignant tumor cells (IC50: approximately 18 microM).
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Mercury(II) Compounds with 1,3-Benzothiazole-2-thione. Spectral, Thermal, and Crystal Structure Studies

TL;DR: In this article, the influence of steric requirements of the ligands on the distortion of the coordination polyhedra accompanied with the relative strength of Hg...N contacts is considered, revealing strong influence of hydrogen bonds on their relative strengths as well as crystal packing requirements of a ligand.
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Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation.

TL;DR: Of all the compounds of this series, spirobipyridopyran (1) inhibited specifically the growth of human melanoma (HBL) cells but not the grow of normal fibroblasts (WI38), and Indolinospirobenzopyrans showed significant cytostatic activities against all tumor cell lines.
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Synthesis and Biological Evaluation of Iodinated and Fluorinated 9-(2-Hydroxypropyl) and 9-(2-Hydroxyethoxy)methyl Purine Nucleoside Analogues

TL;DR: The novel fluorinated and iodinated purine derivatives, and particularly 9a and 9b, appear to demonstrate sufficient cytostatic potency and selectivity to justify further evaluation of their potential.