{"title":"Novel Estrogen Receptor Inhibitory Mechanism for Halogen-containing Endocrine-disrupting Chemicals Discovered by Computer Simulation","authors":"Ayami Matsushima","doi":"10.5059/yukigoseikyokaishi.81.1103","DOIUrl":null,"url":null,"abstract":"Bisphenol A (BPA) is a component used in the manufacture of polycarbonate plastics and epoxy resins around the world; however, it is also well-known as one of the most notorious endocrine-disrupting chemicals. To avoid using BPA as an ingredient, various BPA derivatives and related compounds have been synthesized and the use of these for making polymers has grown significantly; however, the safety of these BPA derivatives, also known as next-generation bisphenols, has not been fully evaluated. We hypothesized that the bisphenol moiety is a privileged structure for binding to nuclear receptors. Here, we summarize the binding ability of next-generation bisphenols to estrogen receptors and show that halogen-containing bisphenols act as coactivator binding inhibitors for estrogen receptor β.","PeriodicalId":17123,"journal":{"name":"Journal of Synthetic Organic Chemistry Japan","volume":"118 3","pages":"0"},"PeriodicalIF":0.2000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Synthetic Organic Chemistry Japan","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5059/yukigoseikyokaishi.81.1103","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Bisphenol A (BPA) is a component used in the manufacture of polycarbonate plastics and epoxy resins around the world; however, it is also well-known as one of the most notorious endocrine-disrupting chemicals. To avoid using BPA as an ingredient, various BPA derivatives and related compounds have been synthesized and the use of these for making polymers has grown significantly; however, the safety of these BPA derivatives, also known as next-generation bisphenols, has not been fully evaluated. We hypothesized that the bisphenol moiety is a privileged structure for binding to nuclear receptors. Here, we summarize the binding ability of next-generation bisphenols to estrogen receptors and show that halogen-containing bisphenols act as coactivator binding inhibitors for estrogen receptor β.