Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на этот ресурс: https://dspace.ncfu.ru/handle/123456789/33022
Название: he Structure of Zinc Chelidonate in the Crystalline Phase, Aqueous Solution and Assessment of the Interaction with Serum Albumin
Авторы: Aksenov, N. A.
Аксенов, Н. А.
Ключевые слова: 4-oxo-4H-pyrans;Bovine serum albumin;Chelidonic acid;Intrinsic protein fluorescence;Zinc;Zinc complexes
Дата публикации: 2026
Издатель: Multidisciplinary Digital Publishing Institute (MDPI)
Библиографическое описание: 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
Источник: Molecules
Краткий осмотр (реферат): 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 (Унифицированный идентификатор ресурса): https://dspace.ncfu.ru/handle/123456789/33022
Располагается в коллекциях:Статьи, проиндексированные в SCOPUS, WOS

Файлы этого ресурса:
Файл Описание РазмерФормат 
scopusresults 4018.pdf
  Доступ ограничен
130.2 kBAdobe PDFПросмотреть/Открыть
WoS 2341.pdf
  Доступ ограничен
113.33 kBAdobe PDFПросмотреть/Открыть


Все ресурсы в архиве электронных ресурсов защищены авторским правом, все права сохранены.