Оlesya V. Pokidova , Veronika O. Novikova , Nina S. Emel’yanova , Ludmila M. Mazina , Alina S. Konyukhova , Alexander V. Kulikov , Gennadii V. Shilov , Nikolai S. Ovanesyan , Tatyana S. Stupina , Natalia A. Sanina
{"title":"一种新型亚硝基铁复合物与 2-甲氧基噻吩酚的结构、性质及在生物系统中的分解,有望用于治疗心血管疾病。","authors":"Оlesya V. Pokidova , Veronika O. Novikova , Nina S. Emel’yanova , Ludmila M. Mazina , Alina S. Konyukhova , Alexander V. Kulikov , Gennadii V. Shilov , Nikolai S. Ovanesyan , Tatyana S. Stupina , Natalia A. Sanina","doi":"10.1016/j.jinorgbio.2024.112747","DOIUrl":null,"url":null,"abstract":"<div><div>A new promising binuclear tetranitrosyl iron complex with 2-methoxythiophenolyl of the composition [Fe<sub>2</sub>(C<sub>7</sub>H<sub>7</sub>OS)<sub>2</sub>(NO)<sub>4</sub>] (complex <strong>1</strong>), which acts on the therapeutic targets of cardiovascular diseases, guanylate and adenylate cyclase, has been synthesized. X-ray diffraction data show the presence of two isoforms of complex <strong>1</strong>; according to quantum chemical calculations, the structure of only the <em>trans</em> isomer is stable in solutions.</div><div>The processes of transformation of complex <strong>1</strong> in DMSO, in aqueous solutions, as well as in the presence of bovine serum albumin, reduced glutathione, and mucin were studied. DMSO promotes the decomposition of the original complex <strong>1</strong> into mononuclear products. In biological systems, the mechanisms of decomposition of the complex <strong>1</strong> differ from aqueous solutions. In albumin solution, a gradual formation of a high-molecular-weight dinitrosyl complex is observed, obtained by coordinating the [Fe(NO)<sub>2</sub>]<sup>+</sup> fragment with the amino acid groups of the protein. In the presence of mucin, an EPR signal from stable mononitrosyl products is observed. The introduction of glutathione into the system of the complex <strong>1</strong> leads to the replacement of one initial thioligand with glutathione. In the model systems under study, a more efficient and prolonged generation of NO groups is observed compared to a buffer solution.</div><div>The obtained data on the influence of the environment on the properties of the complex <strong>1</strong> in combination with a study of their effect on enzymes allow us to recommend it for further study as a potential drug with vasodilator, antianginal, and hypotensive properties.</div></div>","PeriodicalId":364,"journal":{"name":"Journal of Inorganic Biochemistry","volume":"262 ","pages":"Article 112747"},"PeriodicalIF":3.8000,"publicationDate":"2024-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structure, properties, and decomposition in biological systems of a new nitrosyl iron complex with 2-methoxythiophenolyls, promising for the treatment of cardiovascular diseases\",\"authors\":\"Оlesya V. Pokidova , Veronika O. Novikova , Nina S. Emel’yanova , Ludmila M. Mazina , Alina S. Konyukhova , Alexander V. Kulikov , Gennadii V. Shilov , Nikolai S. Ovanesyan , Tatyana S. Stupina , Natalia A. Sanina\",\"doi\":\"10.1016/j.jinorgbio.2024.112747\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A new promising binuclear tetranitrosyl iron complex with 2-methoxythiophenolyl of the composition [Fe<sub>2</sub>(C<sub>7</sub>H<sub>7</sub>OS)<sub>2</sub>(NO)<sub>4</sub>] (complex <strong>1</strong>), which acts on the therapeutic targets of cardiovascular diseases, guanylate and adenylate cyclase, has been synthesized. X-ray diffraction data show the presence of two isoforms of complex <strong>1</strong>; according to quantum chemical calculations, the structure of only the <em>trans</em> isomer is stable in solutions.</div><div>The processes of transformation of complex <strong>1</strong> in DMSO, in aqueous solutions, as well as in the presence of bovine serum albumin, reduced glutathione, and mucin were studied. DMSO promotes the decomposition of the original complex <strong>1</strong> into mononuclear products. In biological systems, the mechanisms of decomposition of the complex <strong>1</strong> differ from aqueous solutions. In albumin solution, a gradual formation of a high-molecular-weight dinitrosyl complex is observed, obtained by coordinating the [Fe(NO)<sub>2</sub>]<sup>+</sup> fragment with the amino acid groups of the protein. In the presence of mucin, an EPR signal from stable mononitrosyl products is observed. The introduction of glutathione into the system of the complex <strong>1</strong> leads to the replacement of one initial thioligand with glutathione. In the model systems under study, a more efficient and prolonged generation of NO groups is observed compared to a buffer solution.</div><div>The obtained data on the influence of the environment on the properties of the complex <strong>1</strong> in combination with a study of their effect on enzymes allow us to recommend it for further study as a potential drug with vasodilator, antianginal, and hypotensive properties.</div></div>\",\"PeriodicalId\":364,\"journal\":{\"name\":\"Journal of Inorganic Biochemistry\",\"volume\":\"262 \",\"pages\":\"Article 112747\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-09-29\",\"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/S0162013424002721\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inorganic Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0162013424002721","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Structure, properties, and decomposition in biological systems of a new nitrosyl iron complex with 2-methoxythiophenolyls, promising for the treatment of cardiovascular diseases
A new promising binuclear tetranitrosyl iron complex with 2-methoxythiophenolyl of the composition [Fe2(C7H7OS)2(NO)4] (complex 1), which acts on the therapeutic targets of cardiovascular diseases, guanylate and adenylate cyclase, has been synthesized. X-ray diffraction data show the presence of two isoforms of complex 1; according to quantum chemical calculations, the structure of only the trans isomer is stable in solutions.
The processes of transformation of complex 1 in DMSO, in aqueous solutions, as well as in the presence of bovine serum albumin, reduced glutathione, and mucin were studied. DMSO promotes the decomposition of the original complex 1 into mononuclear products. In biological systems, the mechanisms of decomposition of the complex 1 differ from aqueous solutions. In albumin solution, a gradual formation of a high-molecular-weight dinitrosyl complex is observed, obtained by coordinating the [Fe(NO)2]+ fragment with the amino acid groups of the protein. In the presence of mucin, an EPR signal from stable mononitrosyl products is observed. The introduction of glutathione into the system of the complex 1 leads to the replacement of one initial thioligand with glutathione. In the model systems under study, a more efficient and prolonged generation of NO groups is observed compared to a buffer solution.
The obtained data on the influence of the environment on the properties of the complex 1 in combination with a study of their effect on enzymes allow us to recommend it for further study as a potential drug with vasodilator, antianginal, and hypotensive properties.
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.