Li-Juan Hu , Xian-Sheng Ye , Kuan Lin , Jie Gao , De-Sen Yang , Guo-Ping Gan , Xi-Ji Shu , Wei Liu , You-Hua Yang
{"title":"菝葜中新的2-芳基苯并呋喃衍生物及其化学分类意义","authors":"Li-Juan Hu , Xian-Sheng Ye , Kuan Lin , Jie Gao , De-Sen Yang , Guo-Ping Gan , Xi-Ji Shu , Wei Liu , You-Hua Yang","doi":"10.1016/j.bse.2025.105073","DOIUrl":null,"url":null,"abstract":"<div><div>One previously undescribed 2-arylbenzofuran derivative (<strong>1</strong>), three stilbenes (<strong>2</strong>-<strong>4</strong>), three acetophenone glycosides (<strong>5</strong>–<strong>7</strong>), three phenylpropanoids (<strong>8</strong>–<strong>10</strong>), and eight flavonoids (<strong>11</strong>–<strong>18</strong>) were isolated from the rhizome of <em>Smilax china</em> L. in this study. NMR spectra elucidated their structures and were compared with previously reported data. Compounds <strong>1</strong>, <strong>5</strong>–<strong>7</strong>, <strong>10</strong>, and <strong>18</strong> were identified for the first time in <em>Smilax china</em> L. The cytotoxicity of the isolated compounds was detected on HeLa cells by the CCK-8 method, and compound <strong>4</strong> was found to possess the highest cytotoxic activity with an IC<sub>50</sub> value of 34.81 ± 1.50 μg/mL. Further studies revealed that the cytotoxic effect of compound <strong>4</strong> on HeLa cells was related to apoptosis and the cell cycle. In addition, the chemotaxonomic significance of the isolated compounds was discussed.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"123 ","pages":"Article 105073"},"PeriodicalIF":1.4000,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A new 2-arylbenzofuran derivative and other constituents from Smilax china L. and their chemotaxonomic significance\",\"authors\":\"Li-Juan Hu , Xian-Sheng Ye , Kuan Lin , Jie Gao , De-Sen Yang , Guo-Ping Gan , Xi-Ji Shu , Wei Liu , You-Hua Yang\",\"doi\":\"10.1016/j.bse.2025.105073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>One previously undescribed 2-arylbenzofuran derivative (<strong>1</strong>), three stilbenes (<strong>2</strong>-<strong>4</strong>), three acetophenone glycosides (<strong>5</strong>–<strong>7</strong>), three phenylpropanoids (<strong>8</strong>–<strong>10</strong>), and eight flavonoids (<strong>11</strong>–<strong>18</strong>) were isolated from the rhizome of <em>Smilax china</em> L. in this study. NMR spectra elucidated their structures and were compared with previously reported data. Compounds <strong>1</strong>, <strong>5</strong>–<strong>7</strong>, <strong>10</strong>, and <strong>18</strong> were identified for the first time in <em>Smilax china</em> L. The cytotoxicity of the isolated compounds was detected on HeLa cells by the CCK-8 method, and compound <strong>4</strong> was found to possess the highest cytotoxic activity with an IC<sub>50</sub> value of 34.81 ± 1.50 μg/mL. Further studies revealed that the cytotoxic effect of compound <strong>4</strong> on HeLa cells was related to apoptosis and the cell cycle. In addition, the chemotaxonomic significance of the isolated compounds was discussed.</div></div>\",\"PeriodicalId\":8799,\"journal\":{\"name\":\"Biochemical Systematics and Ecology\",\"volume\":\"123 \",\"pages\":\"Article 105073\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-07-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical Systematics and Ecology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S030519782500122X\",\"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":"Biochemical Systematics and Ecology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S030519782500122X","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}
A new 2-arylbenzofuran derivative and other constituents from Smilax china L. and their chemotaxonomic significance
One previously undescribed 2-arylbenzofuran derivative (1), three stilbenes (2-4), three acetophenone glycosides (5–7), three phenylpropanoids (8–10), and eight flavonoids (11–18) were isolated from the rhizome of Smilax china L. in this study. NMR spectra elucidated their structures and were compared with previously reported data. Compounds 1, 5–7, 10, and 18 were identified for the first time in Smilax china L. The cytotoxicity of the isolated compounds was detected on HeLa cells by the CCK-8 method, and compound 4 was found to possess the highest cytotoxic activity with an IC50 value of 34.81 ± 1.50 μg/mL. Further studies revealed that the cytotoxic effect of compound 4 on HeLa cells was related to apoptosis and the cell cycle. In addition, the chemotaxonomic significance of the isolated compounds was discussed.
期刊介绍:
Biochemical Systematics and Ecology is devoted to the publication of original papers and reviews, both submitted and invited, in two subject areas: I) the application of biochemistry to problems relating to systematic biology of organisms (biochemical systematics); II) the role of biochemistry in interactions between organisms or between an organism and its environment (biochemical ecology).
In the Biochemical Systematics subject area, comparative studies of the distribution of (secondary) metabolites within a wider taxon (e.g. genus or family) are welcome. Comparative studies, encompassing multiple accessions of each of the taxa within their distribution are particularly encouraged. Welcome are also studies combining classical chemosystematic studies (such as comparative HPLC-MS or GC-MS investigations) with (macro-) molecular phylogenetic studies. Studies that involve the comparative use of compounds to help differentiate among species such as adulterants or substitutes that illustrate the applied use of chemosystematics are welcome. In contrast, studies solely employing macromolecular phylogenetic techniques (gene sequences, RAPD studies etc.) will be considered out of scope. Discouraged are manuscripts that report known or new compounds from a single source taxon without addressing a systematic hypothesis. Also considered out of scope are studies using outdated and hard to reproduce macromolecular techniques such as RAPDs in combination with standard chemosystematic techniques such as GC-FID and GC-MS.