Lijun Chen , Yuanyuan Zhou , Yiyun Geng , Jianjia Liang , Hongyue Ma , Lu Ran , Jingyuan Xu , Zhangshuang Deng , Yiqing Zhou
{"title":"化学蛋白质组学显示橙皮苷和橙皮素是akr11.1 /2抑制剂,具有化学增敏作用","authors":"Lijun Chen , Yuanyuan Zhou , Yiyun Geng , Jianjia Liang , Hongyue Ma , Lu Ran , Jingyuan Xu , Zhangshuang Deng , Yiqing Zhou","doi":"10.1039/d5cc02907d","DOIUrl":null,"url":null,"abstract":"<div><div>The natural flavanone hesperidin and its aglycone hesperetin were identified as human aldo-keto reductase family 1 member C1 (AKR1C1) and AKR1C2 inhibitors <em>via</em> chemoproteomic profiling, which provides mechanistic insight into their chemosensitization effects in cancer therapy.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 68","pages":"Pages 12769-12772"},"PeriodicalIF":4.2000,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chemical proteomics reveals hesperidin and hesperetin as AKR1C1/2 inhibitors with chemosensitization effect†\",\"authors\":\"Lijun Chen , Yuanyuan Zhou , Yiyun Geng , Jianjia Liang , Hongyue Ma , Lu Ran , Jingyuan Xu , Zhangshuang Deng , Yiqing Zhou\",\"doi\":\"10.1039/d5cc02907d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The natural flavanone hesperidin and its aglycone hesperetin were identified as human aldo-keto reductase family 1 member C1 (AKR1C1) and AKR1C2 inhibitors <em>via</em> chemoproteomic profiling, which provides mechanistic insight into their chemosensitization effects in cancer therapy.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 68\",\"pages\":\"Pages 12769-12772\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-08-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734525016179\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734525016179","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Chemical proteomics reveals hesperidin and hesperetin as AKR1C1/2 inhibitors with chemosensitization effect†
The natural flavanone hesperidin and its aglycone hesperetin were identified as human aldo-keto reductase family 1 member C1 (AKR1C1) and AKR1C2 inhibitors via chemoproteomic profiling, which provides mechanistic insight into their chemosensitization effects in cancer therapy.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.