Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/33022
Title: he Structure of Zinc Chelidonate in the Crystalline Phase, Aqueous Solution and Assessment of the Interaction with Serum Albumin
Authors: Aksenov, N. A.
Аксенов, Н. А.
Keywords: 4-oxo-4H-pyrans;Bovine serum albumin;Chelidonic acid;Intrinsic protein fluorescence;Zinc;Zinc complexes
Issue Date: 2026
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
Citation: Kozin S., Dotsenko V., Aksenov N., Bespalov A., Kravtsov A., Lyasota O., Dorohova A., Kindop V., Bobrovnik S., Moiseev A., Ivashchenko L., Gerasimenko E., Huy T.Q., Dzhimak S. The Structure of Zinc Chelidonate in the Crystalline Phase, Aqueous Solution and Assessment of the Interaction with Serum Albumin // Molecules. - 2026. - 31 (9). - art. no. 1378. - DOI: 10.3390/molecules31091378
Series/Report no.: Molecules
Abstract: A zinc complex of chelidonic acid (4-oxo-4H-pyran-2,6-dicarboxylic acid) was obtained by reaction with zinc oxide under isothermal conditions. Its composition was confirmed by elemental and thermogravimetric analyses, and its molecular structure was characterized using NMR and IR spectroscopy. Single-crystal X-ray diffraction revealed that the complex crystallizes as a one-dimensional coordination polymer, [ZnChel(H2O)4]n, in the triclinic space group P-1, featuring a distorted octahedral Zn(II) center coordinated by two chelidonate ligands and four water molecules. This six-coordinate arrangement contrasts with previously described tetra-coordinated Zn–chelidonate complexes. Quantum-chemical calculations and molecular dynamics simulations indicated that, in aqueous solution, Zn(II) preferentially forms a monodentate ZnChel(H2O)5 species, consistent with the solid-state coordination environment. The interaction of the complex with bovine serum albumin (BSA) was examined by fluorescence, UV–Vis absorption, and circular dichroism spectroscopy, revealing a mixed static–dynamic quenching mechanism, moderate binding affinity, and hydrogen-bonding/van der Waals contributions accompanied by alterations in BSA secondary structure. These results expand the structural chemistry of chelidonic acid and provide biophysical insight into the protein-binding behavior of zinc chelidonate, supporting its potential relevance as a zinc-based bioactive compound.
URI: https://dspace.ncfu.ru/handle/123456789/33022
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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