{"title":"Unsymmetrical salen-based oxido VIV: Synthesis, characterization, biomolecular interactions, and anticancer activity","authors":"Deepika Mohapatra , Pratikshya Das Pattanayak , Souvik Chatterjee , Werner Kaminsky , Takahiro Sasamori , Takashi Nakamura , Rupam Dinda","doi":"10.1016/j.jinorgbio.2024.112818","DOIUrl":null,"url":null,"abstract":"<div><div>Three stable oxidovanadium(IV) [V<sup>IV</sup>OL<sup>1–3</sup>] complexes (<strong>1</strong>–<strong>3</strong>) were synthesized through the incorporation of unsymmetrical salen ligands (H<sub>2</sub>L<sup>1−3</sup>). All the ligands are synthesized, and their vanadium compounds were thoroughly characterized by CHNS analysis, various spectroscopy methods (IR, UV–Vis, NMR spectroscopy), and HR–ESI–MS. The structures of <strong>1</strong>–<strong>3</strong> were validated through the single-crystal X-ray analysis. UV–Vis and HR–ESI–MS were used to determine the solution stability of the complexes in the aqueous phase, revealing their stability in aqueous/biological medium. Various spectroscopy techniques were used to study the DNA/BSA binding abilities, and the results indicate that <strong>1</strong>–<strong>3</strong> shows effective biomolecular interactions. The partition coefficient result indicates that <strong>1</strong>–<strong>3</strong> are highly hydrophobic and may easily permeate the cells. Finally, the <em>in vitro</em> anticancer properties of <strong>1</strong>–<strong>3</strong> were determined with two cancerous (HT-29 and A549), and the NIH-3T3 normal cell lines. Among the series, <strong>3</strong> is the most cytotoxic, with IC<sub>50</sub> values of 6.2 ± 0.2 and 5.3 ± 0.4 μM against HT-29 and A549 cell lines respectively. Moreover, the apoptotic cell death mechanism of <strong>1</strong>–<strong>3</strong> was assessed through DAPI, AO/EB, and double staining apoptosis experiments.</div></div>","PeriodicalId":364,"journal":{"name":"Journal of Inorganic Biochemistry","volume":"264 ","pages":"Article 112818"},"PeriodicalIF":3.8000,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inorganic Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S016201342400343X","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Three stable oxidovanadium(IV) [VIVOL1–3] complexes (1–3) were synthesized through the incorporation of unsymmetrical salen ligands (H2L1−3). All the ligands are synthesized, and their vanadium compounds were thoroughly characterized by CHNS analysis, various spectroscopy methods (IR, UV–Vis, NMR spectroscopy), and HR–ESI–MS. The structures of 1–3 were validated through the single-crystal X-ray analysis. UV–Vis and HR–ESI–MS were used to determine the solution stability of the complexes in the aqueous phase, revealing their stability in aqueous/biological medium. Various spectroscopy techniques were used to study the DNA/BSA binding abilities, and the results indicate that 1–3 shows effective biomolecular interactions. The partition coefficient result indicates that 1–3 are highly hydrophobic and may easily permeate the cells. Finally, the in vitro anticancer properties of 1–3 were determined with two cancerous (HT-29 and A549), and the NIH-3T3 normal cell lines. Among the series, 3 is the most cytotoxic, with IC50 values of 6.2 ± 0.2 and 5.3 ± 0.4 μM against HT-29 and A549 cell lines respectively. Moreover, the apoptotic cell death mechanism of 1–3 was assessed through DAPI, AO/EB, and double staining apoptosis experiments.
期刊介绍:
The Journal of Inorganic Biochemistry is an established international forum for research in all aspects of Biological Inorganic Chemistry. Original papers of a high scientific level are published in the form of Articles (full length papers), Short Communications, Focused Reviews and Bioinorganic Methods. Topics include: the chemistry, structure and function of metalloenzymes; the interaction of inorganic ions and molecules with proteins and nucleic acids; the synthesis and properties of coordination complexes of biological interest including both structural and functional model systems; the function of metal- containing systems in the regulation of gene expression; the role of metals in medicine; the application of spectroscopic methods to determine the structure of metallobiomolecules; the preparation and characterization of metal-based biomaterials; and related systems. The emphasis of the Journal is on the structure and mechanism of action of metallobiomolecules.