Wei-Fang Su , Ni-Ping Li , Rui-Qin Cui , Fen Liu , Mu Chen , Xin-Yue Wu , Min-Jing Cheng , Jia-Qing Cao , Wei Huang , Xiao-Qi Zhang , Wen-Cai Ye , Lei Wang
{"title":"赤霉素A - F:从赤霉中提取的抗菌间苯三酚萜类加合物","authors":"Wei-Fang Su , Ni-Ping Li , Rui-Qin Cui , Fen Liu , Mu Chen , Xin-Yue Wu , Min-Jing Cheng , Jia-Qing Cao , Wei Huang , Xiao-Qi Zhang , Wen-Cai Ye , Lei Wang","doi":"10.1039/d5qo00172b","DOIUrl":null,"url":null,"abstract":"<div><div>Thrysaxinones A–F (), six new phloroglucinol-terpenoid adducts (PTAs), were isolated from <em>Thryptomene saxicola</em>. Their structures and absolute configurations were elucidated by extensive spectroscopic analysis, X-ray crystallography, and quantum chemical calculations. Compounds represent unprecedented PTAs with gorgonane- or oplopane-type sesquiterpenoid moieties. Notably, compound features an unusual 11-oxa-tricyclo[6.2.1.0<sup>4,9</sup>]undecane core. Compound is a unique PTA with a new carbon skeleton formed by an acylphloroglucinol unit coupled with a bicyclogermacrene-type sesquiterpenoid moiety. The plausible biogenetic pathways for compounds were proposed. Moreover, compounds , , , and exhibited significant antibacterial activities against clinical methicillin-resistant <em>Staphylococcus aureus</em> (MRSA) strains. Compound , the most potent one, could rapidly and effectively eradicate bacteria by inducing hyperpolarization and disrupting cell membrane integrity.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 14","pages":"Pages 4037-4044"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thrysaxinones A–F: antibacterial phloroglucinol-terpenoid adducts from Thryptomene saxicola†\",\"authors\":\"Wei-Fang Su , Ni-Ping Li , Rui-Qin Cui , Fen Liu , Mu Chen , Xin-Yue Wu , Min-Jing Cheng , Jia-Qing Cao , Wei Huang , Xiao-Qi Zhang , Wen-Cai Ye , Lei Wang\",\"doi\":\"10.1039/d5qo00172b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Thrysaxinones A–F (), six new phloroglucinol-terpenoid adducts (PTAs), were isolated from <em>Thryptomene saxicola</em>. Their structures and absolute configurations were elucidated by extensive spectroscopic analysis, X-ray crystallography, and quantum chemical calculations. Compounds represent unprecedented PTAs with gorgonane- or oplopane-type sesquiterpenoid moieties. Notably, compound features an unusual 11-oxa-tricyclo[6.2.1.0<sup>4,9</sup>]undecane core. Compound is a unique PTA with a new carbon skeleton formed by an acylphloroglucinol unit coupled with a bicyclogermacrene-type sesquiterpenoid moiety. The plausible biogenetic pathways for compounds were proposed. Moreover, compounds , , , and exhibited significant antibacterial activities against clinical methicillin-resistant <em>Staphylococcus aureus</em> (MRSA) strains. Compound , the most potent one, could rapidly and effectively eradicate bacteria by inducing hyperpolarization and disrupting cell membrane integrity.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 14\",\"pages\":\"Pages 4037-4044\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2052412925002396\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412925002396","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Thrysaxinones A–F: antibacterial phloroglucinol-terpenoid adducts from Thryptomene saxicola†
Thrysaxinones A–F (), six new phloroglucinol-terpenoid adducts (PTAs), were isolated from Thryptomene saxicola. Their structures and absolute configurations were elucidated by extensive spectroscopic analysis, X-ray crystallography, and quantum chemical calculations. Compounds represent unprecedented PTAs with gorgonane- or oplopane-type sesquiterpenoid moieties. Notably, compound features an unusual 11-oxa-tricyclo[6.2.1.04,9]undecane core. Compound is a unique PTA with a new carbon skeleton formed by an acylphloroglucinol unit coupled with a bicyclogermacrene-type sesquiterpenoid moiety. The plausible biogenetic pathways for compounds were proposed. Moreover, compounds , , , and exhibited significant antibacterial activities against clinical methicillin-resistant Staphylococcus aureus (MRSA) strains. Compound , the most potent one, could rapidly and effectively eradicate bacteria by inducing hyperpolarization and disrupting cell membrane integrity.