Publications by authors named "G Orgovan"

Article Synopsis
  • The study focuses on adrenaline, noradrenaline, and related compounds, analyzing their acid-base properties through H NMR-pH titrations.
  • Three macroscopic and twelve microscopic protonation constants for these molecules were quantified, providing insight into their basicities.
  • The research suggests that understanding these basicities could be essential for interpreting the biochemical behavior of catecholamines, including dopamine.
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Article Synopsis
  • A new method for determining pH using 1H NMR was created, eliminating the need for traditional glass or electrode measurements.
  • The method involves organic compounds with known basicity, allowing for accurate tracking of how their proton shifts change with pH.
  • Six selected indicator molecules can cover the entire pH scale, and the technique was tested at two different ionic strengths (1.00 and 0.15 M).
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Dopamine and 4 related compounds were studied by H NMR-pH titrations and a case-tailored evaluation method. The resulting acid-base properties of dopamine are quantified in terms of 3 macroscopic and 12 microscopic protonation constants and the concomitant 3 interactivity parameters. The species- and site-specific basicities are interpreted by means of inductive and shielding effects through various intra- and intermolecular comparisons.

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In the present study, several Cu chelators [2,2'-biquinoline, 8-hydroxiquinoline (oxine), ammonium pyrrolidinedithiocarbamate (APDTC), Dp44mT, dithizone, neocuproine] were used to study Cu uptake, depletion and localization in different cancer cell lines. To better understand the concentration dependent fluctuations in the Cu intracellular metal content and Cu-dependent in vitro antiproliferative data, the conditional stability constants of the Cu complex species of the investigated ligands were calculated. Each investigated chelator increased the intracellular Cu content on HT-29 cells causing Cu accumulation depending on the amount of the free Cu(II).

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Biorelevant, isomer-specific physicochemical parameters of resveratrol, a multifunctional component in red wines, with cardioprotective, anti-Alzheimer and several other pharmacologic activities were determined. The parameters include site-specific basicities, lipophilicities, solubilities and diffusion constants for the two geometric isomers. The protonation equilibria of (E)- and (Z)-resveratrol were monitored by H NMR-pH titrations.

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