Chenliang Zhao , Yaxin Yang , Abdullah Al Mamun , Lei Wang , Guangjie Li , Jianghai Ye , Jingjie Zhang , Lutai Pan , Kang He , Juan Zou , Hongjie Zhang
{"title":"Cytotoxic and anticoagulative diterpenoid glycosides from Pteris decrescens","authors":"Chenliang Zhao , Yaxin Yang , Abdullah Al Mamun , Lei Wang , Guangjie Li , Jianghai Ye , Jingjie Zhang , Lutai Pan , Kang He , Juan Zou , Hongjie Zhang","doi":"10.1016/j.phytochem.2025.114643","DOIUrl":null,"url":null,"abstract":"<div><div>Diterpenoids from the genus <em>Pteris</em> have demonstrated consistent anticancer properties. In the present study, five previously undescribed (<strong>1-5</strong>) and four known diterpenoids (<strong>6–9</strong>) were isolated from the 95 % methanol extract of <em>P. decrescens</em>. Among them, decrescensin A (<strong>1</strong>), represents the first naturally occurring example of a 15(8 → 9)-<em>abeo</em>-<em>ent</em>-kauranoid. The structures of these compounds were established based on their spectroscopic data and single-crystal X-ray diffraction. Compounds <strong>1</strong>–<strong>9</strong> have been evaluated for their cytotoxic effects against a panel of cancer cell lines including HeLa, HepG2, A549 and SW480. Compound <strong>1</strong> showed significant activity in SW480 cells with an IC<sub>50</sub> value of 0.46 μM. In addition, compounds <strong>4</strong> and <strong>6</strong> displayed a mild prolongation effect on activated partial thromboplastin time.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"240 ","pages":"Article 114643"},"PeriodicalIF":3.4000,"publicationDate":"2025-08-13","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/S0031942225002663","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
Diterpenoids from the genus Pteris have demonstrated consistent anticancer properties. In the present study, five previously undescribed (1-5) and four known diterpenoids (6–9) were isolated from the 95 % methanol extract of P. decrescens. Among them, decrescensin A (1), represents the first naturally occurring example of a 15(8 → 9)-abeo-ent-kauranoid. The structures of these compounds were established based on their spectroscopic data and single-crystal X-ray diffraction. Compounds 1–9 have been evaluated for their cytotoxic effects against a panel of cancer cell lines including HeLa, HepG2, A549 and SW480. Compound 1 showed significant activity in SW480 cells with an IC50 value of 0.46 μM. In addition, compounds 4 and 6 displayed a mild prolongation effect on activated partial thromboplastin time.
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.