{"title":"花楸茎中的色素。","authors":"Sakunchai Khumsubdee , Vilailak Prachyawarakorn , Chulabhorn Mahidol , Poonsakdi Ploypradith , Somsak Ruchirawat , Phanruethai Pailee","doi":"10.1080/14786419.2025.2462968","DOIUrl":null,"url":null,"abstract":"<div><div>Four new chromones, named harforamone A (<strong>1</strong>), harforamone B (<strong>2</strong>), harforamone C (<strong>3</strong>), and harforamone D (<strong>4</strong>), together with six known compounds (<strong>5</strong>–<strong>10</strong>) were isolated from the dichloromethane extract of the stems of <em>Harrisonia perforata</em>. The chemical structures of four new compounds were elucidated by spectroscopic analysis, including 1D, 2D NMR and HRESIMS data. The known compounds were identified by comparing their spectroscopic data with the previously reported data. Compounds <strong>7</strong> and <strong>8</strong> were isolated for the first time from the Rutaceae family. The <em>in vitro</em> cytotoxic activity against six human cancer cell lines of the tested compounds was evaluated, but none of them showed any significant activity; only perforamone C (<strong>5</strong>) showed moderate cytotoxicity against cervical cancer cell line (HeLa).</div></div>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":"40 9","pages":"Pages 2299-2305"},"PeriodicalIF":1.6000,"publicationDate":"2026-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chromones from stems of Harrisonia perforata\",\"authors\":\"Sakunchai Khumsubdee , Vilailak Prachyawarakorn , Chulabhorn Mahidol , Poonsakdi Ploypradith , Somsak Ruchirawat , Phanruethai Pailee\",\"doi\":\"10.1080/14786419.2025.2462968\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Four new chromones, named harforamone A (<strong>1</strong>), harforamone B (<strong>2</strong>), harforamone C (<strong>3</strong>), and harforamone D (<strong>4</strong>), together with six known compounds (<strong>5</strong>–<strong>10</strong>) were isolated from the dichloromethane extract of the stems of <em>Harrisonia perforata</em>. The chemical structures of four new compounds were elucidated by spectroscopic analysis, including 1D, 2D NMR and HRESIMS data. The known compounds were identified by comparing their spectroscopic data with the previously reported data. Compounds <strong>7</strong> and <strong>8</strong> were isolated for the first time from the Rutaceae family. The <em>in vitro</em> cytotoxic activity against six human cancer cell lines of the tested compounds was evaluated, but none of them showed any significant activity; only perforamone C (<strong>5</strong>) showed moderate cytotoxicity against cervical cancer cell line (HeLa).</div></div>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\"40 9\",\"pages\":\"Pages 2299-2305\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2026-05-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1478641925000622\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1478641925000622","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/3 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
摘要
从刺果藤茎二氯甲烷提取物中分离到4个新激素，分别命名为harforamone A(1)、harforamone B(2)、harforamone C(3)和harforamone D(4)，以及6个已知化合物（5-10）。通过一维、二维核磁共振和HRESIMS数据等光谱分析，确定了4个新化合物的化学结构。通过将已知化合物的光谱数据与先前报道的数据进行比较，确定了已知化合物。化合物7和8为首次从芸香科植物中分离得到。体外对6种人类癌细胞的细胞毒活性进行了评价，但均未显示出显著活性；只有perform one C(5)对宫颈癌细胞系（HeLa）表现出中等的细胞毒性。
Four new chromones, named harforamone A (1), harforamone B (2), harforamone C (3), and harforamone D (4), together with six known compounds (5–10) were isolated from the dichloromethane extract of the stems of Harrisonia perforata. The chemical structures of four new compounds were elucidated by spectroscopic analysis, including 1D, 2D NMR and HRESIMS data. The known compounds were identified by comparing their spectroscopic data with the previously reported data. Compounds 7 and 8 were isolated for the first time from the Rutaceae family. The in vitro cytotoxic activity against six human cancer cell lines of the tested compounds was evaluated, but none of them showed any significant activity; only perforamone C (5) showed moderate cytotoxicity against cervical cancer cell line (HeLa).
期刊介绍：
The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds.
The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal.
Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section.
All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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