{"title":"(±)-Harmansenoids A和B,两对具有心脏保护作用的新间苯三酚。","authors":"Silian Zhou, Junhui Du","doi":"10.1080/14786419.2025.2567636","DOIUrl":null,"url":null,"abstract":"<p><p>Six new phloroglucinols which were assigned as two pairs of natural enantiomer (±)-Harmansenoids A (<b>1</b>) and B (<b>2</b>) together with two known ones were separated from <i>Hypericum monogynum</i> L (Hypericaceae). The planer and stereochemical structure were elucidated by using NMR, HR-ESI-MS, ECD analysis and computational chemistry method. Further, the cardioprotective activity of all compounds were evaluated by MTT method. Among them, compound <b>3</b> exhibited the strongest effect than other isolates.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"1-5"},"PeriodicalIF":1.6000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"(±)-Harmansenoids A and B, two pairs of new phloroglucinols with cardioprotective effects from <i>Hypericum monogynum</i> L. (Hypericaceae).\",\"authors\":\"Silian Zhou, Junhui Du\",\"doi\":\"10.1080/14786419.2025.2567636\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Six new phloroglucinols which were assigned as two pairs of natural enantiomer (±)-Harmansenoids A (<b>1</b>) and B (<b>2</b>) together with two known ones were separated from <i>Hypericum monogynum</i> L (Hypericaceae). The planer and stereochemical structure were elucidated by using NMR, HR-ESI-MS, ECD analysis and computational chemistry method. Further, the cardioprotective activity of all compounds were evaluated by MTT method. Among them, compound <b>3</b> exhibited the strongest effect than other isolates.</p>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\" \",\"pages\":\"1-5\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1080/14786419.2025.2567636\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2025.2567636","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
(±)-Harmansenoids A and B, two pairs of new phloroglucinols with cardioprotective effects from Hypericum monogynum L. (Hypericaceae).
Six new phloroglucinols which were assigned as two pairs of natural enantiomer (±)-Harmansenoids A (1) and B (2) together with two known ones were separated from Hypericum monogynum L (Hypericaceae). The planer and stereochemical structure were elucidated by using NMR, HR-ESI-MS, ECD analysis and computational chemistry method. Further, the cardioprotective activity of all compounds were evaluated by MTT method. Among them, compound 3 exhibited the strongest effect than other isolates.
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.