{"title":"大戟醇B是一种从大戟根中分离得到的新的非正枞烷二萜。","authors":"Young Sook Yun , Miki Shimamura , Haruhiko Fukaya , Hiroyuki Fuchino , Nobuo Kawahara , Hideshi Inoue","doi":"10.1016/j.phytol.2024.12.009","DOIUrl":null,"url":null,"abstract":"<div><div>A new nor-<em>ent</em>-abietane diterpenoid (<strong>1</strong>) was isolated from the root of <em>Euphorbia lathyris</em> L. Its structure and absolute configuration were determined based on data obtained from HRESIMS, NMR, and X-ray diffraction analysis. This compound, named lathyrisol B, is a nor-<em>ent</em>-abietane diterpenoid with an exocyclic olefin at the C-4 position. Lathyrisol B was found to stimulate the expression of a reporter gene under the control of amino acid response elements (AARE) of C/EBP homologous protein (CHOP) promoter in MIA PaCa-2 cells, human pancreatic cancer cells.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"65 ","pages":"Pages 113-116"},"PeriodicalIF":1.4000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lathyrisol B, a new nor-ent-abietane diterpenoid from roots of Euphorbia lathyris L.\",\"authors\":\"Young Sook Yun , Miki Shimamura , Haruhiko Fukaya , Hiroyuki Fuchino , Nobuo Kawahara , Hideshi Inoue\",\"doi\":\"10.1016/j.phytol.2024.12.009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A new nor-<em>ent</em>-abietane diterpenoid (<strong>1</strong>) was isolated from the root of <em>Euphorbia lathyris</em> L. Its structure and absolute configuration were determined based on data obtained from HRESIMS, NMR, and X-ray diffraction analysis. This compound, named lathyrisol B, is a nor-<em>ent</em>-abietane diterpenoid with an exocyclic olefin at the C-4 position. Lathyrisol B was found to stimulate the expression of a reporter gene under the control of amino acid response elements (AARE) of C/EBP homologous protein (CHOP) promoter in MIA PaCa-2 cells, human pancreatic cancer cells.</div></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"65 \",\"pages\":\"Pages 113-116\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry Letters\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1874390024001691\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1874390024001691","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Lathyrisol B, a new nor-ent-abietane diterpenoid from roots of Euphorbia lathyris L.
A new nor-ent-abietane diterpenoid (1) was isolated from the root of Euphorbia lathyris L. Its structure and absolute configuration were determined based on data obtained from HRESIMS, NMR, and X-ray diffraction analysis. This compound, named lathyrisol B, is a nor-ent-abietane diterpenoid with an exocyclic olefin at the C-4 position. Lathyrisol B was found to stimulate the expression of a reporter gene under the control of amino acid response elements (AARE) of C/EBP homologous protein (CHOP) promoter in MIA PaCa-2 cells, human pancreatic cancer cells.
期刊介绍:
Phytochemistry Letters invites rapid communications on all aspects of natural product research including:
• Structural elucidation of natural products
• Analytical evaluation of herbal medicines
• Clinical efficacy, safety and pharmacovigilance of herbal medicines
• Natural product biosynthesis
• Natural product synthesis and chemical modification
• Natural product metabolism
• Chemical ecology
• Biotechnology
• Bioassay-guided isolation
• Pharmacognosy
• Pharmacology of natural products
• Metabolomics
• Ethnobotany and traditional usage
• Genetics of natural products
Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.