{"title":"桑科无花果的化学成分。","authors":"Eitel Ngoh Misse Mouelle, Mohamed Foundikou Nsangou, Vanini Samiyatou Michiren Mandou, Jean Duplex Wansi, Sergi Herve Akone, Emmanuel Ngeufa Happi","doi":"10.1515/znc-2022-0165","DOIUrl":null,"url":null,"abstract":"<p><p>Phytochemical investigation of the aerial roots of <i>Ficus sur</i>, a Cameroonian medicinal plant, resulted in a previously undescribed cerebroside, suroside <b>(1)</b>, in addition to its aglycon congener suramide <b>(2)</b>. Moreover, six known natural products including alpinumisoflavone <b>(3)</b>, wighteone metabolite <b>(4)</b>, oleanolic acid <b>(5)</b>, <i>β</i>-sitosterol <b>(6)</b>, <i>β</i>-sitosterol-3-<i>O</i>-<i>β</i>-D-glucopyranoside <b>(7),</b> and epi-<i>ѱ</i>-taraxastanolone <b>(8)</b> were identified. The structures of the previously undescribed compounds were determined by analysis of 1D and 2D-NMR (One and two dimensional nuclear magnetic resonance), mass spectrometry, chemical conversion, and by comparison of these data with those from the literature. Wighteone metabolite <b>(4)</b> exhibited a weak cytotoxic activity against the human HepG2 hepatocellular carcinoma cells with an IC<sub>50</sub> value of 51.9 µM.</p>","PeriodicalId":49344,"journal":{"name":"Zeitschrift Fur Naturforschung Section C-A Journal of Biosciences","volume":"78 5-6","pages":"201-207"},"PeriodicalIF":1.8000,"publicationDate":"2023-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Chemical constituents from <i>Ficus sur</i> Forssk (Moraceae).\",\"authors\":\"Eitel Ngoh Misse Mouelle, Mohamed Foundikou Nsangou, Vanini Samiyatou Michiren Mandou, Jean Duplex Wansi, Sergi Herve Akone, Emmanuel Ngeufa Happi\",\"doi\":\"10.1515/znc-2022-0165\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Phytochemical investigation of the aerial roots of <i>Ficus sur</i>, a Cameroonian medicinal plant, resulted in a previously undescribed cerebroside, suroside <b>(1)</b>, in addition to its aglycon congener suramide <b>(2)</b>. Moreover, six known natural products including alpinumisoflavone <b>(3)</b>, wighteone metabolite <b>(4)</b>, oleanolic acid <b>(5)</b>, <i>β</i>-sitosterol <b>(6)</b>, <i>β</i>-sitosterol-3-<i>O</i>-<i>β</i>-D-glucopyranoside <b>(7),</b> and epi-<i>ѱ</i>-taraxastanolone <b>(8)</b> were identified. The structures of the previously undescribed compounds were determined by analysis of 1D and 2D-NMR (One and two dimensional nuclear magnetic resonance), mass spectrometry, chemical conversion, and by comparison of these data with those from the literature. Wighteone metabolite <b>(4)</b> exhibited a weak cytotoxic activity against the human HepG2 hepatocellular carcinoma cells with an IC<sub>50</sub> value of 51.9 µM.</p>\",\"PeriodicalId\":49344,\"journal\":{\"name\":\"Zeitschrift Fur Naturforschung Section C-A Journal of Biosciences\",\"volume\":\"78 5-6\",\"pages\":\"201-207\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2023-05-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zeitschrift Fur Naturforschung Section C-A Journal of Biosciences\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1515/znc-2022-0165\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift Fur Naturforschung Section C-A Journal of Biosciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1515/znc-2022-0165","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 1
摘要
对喀麦隆药用植物Ficus sur的气生根进行植物化学研究,发现了一种以前未被描述过的脑苷,suroside(1),以及其糖醛酸同属物suramide(2)。此外,还鉴定了六种已知的天然产物,包括alpinumisoflavone(3),白豆酮代谢物(4),齐ole果酸(5),β-谷甾醇(6),β-谷甾醇-3- o -β-D-glucopyranoside(7)和epi-ѱ-taraxastanolone(8)。通过1D和2d核磁共振(一维和二维核磁共振)、质谱分析、化学转化分析以及与文献数据的比较,确定了先前描述的化合物的结构。怀特酮代谢物(4)对人HepG2肝癌细胞具有较弱的细胞毒活性,IC50值为51.9µM。
Chemical constituents from Ficus sur Forssk (Moraceae).
Phytochemical investigation of the aerial roots of Ficus sur, a Cameroonian medicinal plant, resulted in a previously undescribed cerebroside, suroside (1), in addition to its aglycon congener suramide (2). Moreover, six known natural products including alpinumisoflavone (3), wighteone metabolite (4), oleanolic acid (5), β-sitosterol (6), β-sitosterol-3-O-β-D-glucopyranoside (7), and epi-ѱ-taraxastanolone (8) were identified. The structures of the previously undescribed compounds were determined by analysis of 1D and 2D-NMR (One and two dimensional nuclear magnetic resonance), mass spectrometry, chemical conversion, and by comparison of these data with those from the literature. Wighteone metabolite (4) exhibited a weak cytotoxic activity against the human HepG2 hepatocellular carcinoma cells with an IC50 value of 51.9 µM.
期刊介绍:
A Journal of Biosciences: Zeitschrift für Naturforschung C (ZNC) is an international scientific journal and a community resource for the emerging field of natural and natural-like products. The journal publishes original research on the isolation (including structure elucidation), bio-chemical synthesis and bioactivities of natural products, their biochemistry, pharmacology, biotechnology, and their biological activity and innovative developed computational methods for predicting the structure and/or function of natural products. A Journal of Biosciences: Zeitschrift für Naturforschung C (ZNC) welcomes research papers in fields on the chemistry-biology boundary which address scientific ideas and approaches to generate and understand natural compounds on a molecular level and/or use them to stimulate and manipulate biological processes.