{"title":"分光光度法测定新型功能性席夫碱及其外周CoII和CuII酞菁在阿尔茨海默病治疗中的体外胆碱能酶抑制电位","authors":"Halise Yalazan , Gökçe Seyhan , Ceren Boğuşlu , Burak Barut , Halit Kantekin","doi":"10.1016/j.poly.2025.117567","DOIUrl":null,"url":null,"abstract":"<div><div>Cholinergic neurons and presynaptic indicators of the cholinergic system gradually disappear as a result of neurodegenerative disorders, including Alzheimer’s disease (AD), one of the most prevalent causes of dementia. By inhibiting acetylcholinesterase (AChE) and thus reducing the rate of acetylcholine hydrolysis, these effects can be counteracted. Anticholinesterase medications that have reversible inhibitory effects are therefore used to treat neurodegenerative illnesses. This work involved the synthesis of Schiff base compounds (<strong>Schiffb.OH/CN</strong>) and their cobalt (<strong>Schiffb.CoPc</strong>) and copper (<strong>Schiffb.CuPc</strong>) phthalocyanine compounds, as well as spectrophotometric analysis of their <em>in vitro</em> cholinergic enzyme inhibitory potentials. Overall, it was found that, when compared to the other compounds examined, <strong>Schiffb.CuPc</strong> was the most potent inhibitor. Furthermore, it exhibited statistically comparable results to the positive control, galantamine (26.17 ± 0.52 µM). However, at the concentrations examined, it was shown that the compounds exhibited no action against BuChE. The compounds may be selective for AChE, according to this research.</div></div>","PeriodicalId":20278,"journal":{"name":"Polyhedron","volume":"277 ","pages":"Article 117567"},"PeriodicalIF":2.4000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Spectrophotometric in vitro cholinergic enzyme inhibitory potentials of novel functional Schiff bases and their peripheral CoII and CuII phthalocyanines in the treatment of Alzheimer’s disease\",\"authors\":\"Halise Yalazan , Gökçe Seyhan , Ceren Boğuşlu , Burak Barut , Halit Kantekin\",\"doi\":\"10.1016/j.poly.2025.117567\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cholinergic neurons and presynaptic indicators of the cholinergic system gradually disappear as a result of neurodegenerative disorders, including Alzheimer’s disease (AD), one of the most prevalent causes of dementia. By inhibiting acetylcholinesterase (AChE) and thus reducing the rate of acetylcholine hydrolysis, these effects can be counteracted. Anticholinesterase medications that have reversible inhibitory effects are therefore used to treat neurodegenerative illnesses. This work involved the synthesis of Schiff base compounds (<strong>Schiffb.OH/CN</strong>) and their cobalt (<strong>Schiffb.CoPc</strong>) and copper (<strong>Schiffb.CuPc</strong>) phthalocyanine compounds, as well as spectrophotometric analysis of their <em>in vitro</em> cholinergic enzyme inhibitory potentials. Overall, it was found that, when compared to the other compounds examined, <strong>Schiffb.CuPc</strong> was the most potent inhibitor. Furthermore, it exhibited statistically comparable results to the positive control, galantamine (26.17 ± 0.52 µM). However, at the concentrations examined, it was shown that the compounds exhibited no action against BuChE. The compounds may be selective for AChE, according to this research.</div></div>\",\"PeriodicalId\":20278,\"journal\":{\"name\":\"Polyhedron\",\"volume\":\"277 \",\"pages\":\"Article 117567\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polyhedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0277538725001810\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polyhedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0277538725001810","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Spectrophotometric in vitro cholinergic enzyme inhibitory potentials of novel functional Schiff bases and their peripheral CoII and CuII phthalocyanines in the treatment of Alzheimer’s disease
Cholinergic neurons and presynaptic indicators of the cholinergic system gradually disappear as a result of neurodegenerative disorders, including Alzheimer’s disease (AD), one of the most prevalent causes of dementia. By inhibiting acetylcholinesterase (AChE) and thus reducing the rate of acetylcholine hydrolysis, these effects can be counteracted. Anticholinesterase medications that have reversible inhibitory effects are therefore used to treat neurodegenerative illnesses. This work involved the synthesis of Schiff base compounds (Schiffb.OH/CN) and their cobalt (Schiffb.CoPc) and copper (Schiffb.CuPc) phthalocyanine compounds, as well as spectrophotometric analysis of their in vitro cholinergic enzyme inhibitory potentials. Overall, it was found that, when compared to the other compounds examined, Schiffb.CuPc was the most potent inhibitor. Furthermore, it exhibited statistically comparable results to the positive control, galantamine (26.17 ± 0.52 µM). However, at the concentrations examined, it was shown that the compounds exhibited no action against BuChE. The compounds may be selective for AChE, according to this research.
期刊介绍:
Polyhedron publishes original, fundamental, experimental and theoretical work of the highest quality in all the major areas of inorganic chemistry. This includes synthetic chemistry, coordination chemistry, organometallic chemistry, bioinorganic chemistry, and solid-state and materials chemistry.
Papers should be significant pieces of work, and all new compounds must be appropriately characterized. The inclusion of single-crystal X-ray structural data is strongly encouraged, but papers reporting only the X-ray structure determination of a single compound will usually not be considered. Papers on solid-state or materials chemistry will be expected to have a significant molecular chemistry component (such as the synthesis and characterization of the molecular precursors and/or a systematic study of the use of different precursors or reaction conditions) or demonstrate a cutting-edge application (for example inorganic materials for energy applications). Papers dealing only with stability constants are not considered.