Yuan Zong , Jun-jie Yang , Hui-ming Zhang , Lin-lin Li , Ping-lin Li
{"title":"Eleven undescribed sesquiterpenoids with multiple skeleton types and cytotoxicity from the South China Sea soft coral Lemnalia sp.","authors":"Yuan Zong , Jun-jie Yang , Hui-ming Zhang , Lin-lin Li , Ping-lin Li","doi":"10.1016/j.phytochem.2025.114576","DOIUrl":null,"url":null,"abstract":"<div><div>Marine organisms have great potential for medical and bioproducts applications, with corals having been in the spotlight as an important research target for the discovery of new bioactive marine natural products. Eleven undescribed sesquiterpenoids, named lemnalinoids A−K (<strong>1</strong>−<strong>11</strong>), and one known sesquiterpenoid (<strong>12</strong>) were isolated from the South China Sea soft coral <em>Lemnalia</em> sp. The structures and absolute configurations of new compounds were elucidated by extensive analysis of spectroscopic data, single crystal X-ray diffraction, quantum chemical calculations and TDDFT-ECD calculations. Compounds <strong>1</strong>−<strong>3</strong> are unusual sesquiterpenoids with spironolactone structure, of which compound <strong>1</strong> is an uncommon brominated sesquiterpenoid of soft coral origin. Compounds <strong>4</strong>−<strong>6</strong> and <strong>12</strong> are four rare sesquiterpenoid alkaloids from soft coral, and compound <strong>7</strong> is an unusual sesquiterpenoid with a 6/5/6 tricyclic skeleton system, besides, compounds <strong>8</strong>−<strong>11</strong> are undescribed nardosinane and nornardosinane sesquiterpenoids. In the bioactivity assay, compound <strong>2</strong> exhibited cytotoxicity against NCI–H446 cell lines with an IC<sub>50</sub> value of 19.32 μM, and the molecular docking results indicated that the mechanism of action may be related to its inhibitory effect on the target proteins VEGFR2, CD56, and PARP.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"238 ","pages":"Article 114576"},"PeriodicalIF":3.4000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942225001992","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Marine organisms have great potential for medical and bioproducts applications, with corals having been in the spotlight as an important research target for the discovery of new bioactive marine natural products. Eleven undescribed sesquiterpenoids, named lemnalinoids A−K (1−11), and one known sesquiterpenoid (12) were isolated from the South China Sea soft coral Lemnalia sp. The structures and absolute configurations of new compounds were elucidated by extensive analysis of spectroscopic data, single crystal X-ray diffraction, quantum chemical calculations and TDDFT-ECD calculations. Compounds 1−3 are unusual sesquiterpenoids with spironolactone structure, of which compound 1 is an uncommon brominated sesquiterpenoid of soft coral origin. Compounds 4−6 and 12 are four rare sesquiterpenoid alkaloids from soft coral, and compound 7 is an unusual sesquiterpenoid with a 6/5/6 tricyclic skeleton system, besides, compounds 8−11 are undescribed nardosinane and nornardosinane sesquiterpenoids. In the bioactivity assay, compound 2 exhibited cytotoxicity against NCI–H446 cell lines with an IC50 value of 19.32 μM, and the molecular docking results indicated that the mechanism of action may be related to its inhibitory effect on the target proteins VEGFR2, CD56, and PARP.
期刊介绍:
Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.