Deri Hu , Zhenyu Liu , Yue Yu , Chenghao Wu , Jinze Liu , Dongzhou Kang , Junzhe Min , Mingshan Zheng
{"title":"榆树的化学成分及其化学分类学意义","authors":"Deri Hu , Zhenyu Liu , Yue Yu , Chenghao Wu , Jinze Liu , Dongzhou Kang , Junzhe Min , Mingshan Zheng","doi":"10.1016/j.bse.2024.104907","DOIUrl":null,"url":null,"abstract":"<div><div>A phytochemical study of the leaves of <em>Ulmus pumila</em> L. led to the isolation of 32 compounds, including fourteen flavonoids, which include flavonols (<strong>1</strong>–<strong>6</strong>), dihydroflavones (<strong>7</strong>–<strong>11</strong>), and dihydroflavonols (<strong>12</strong>–<strong>14</strong>), five terpenoids, which include megastigmane glycosides (<strong>15</strong>–<strong>17</strong>) and triterpenoids (<strong>18</strong>–<strong>19</strong>), four sugars (<strong>20</strong>–<strong>23</strong>), one phenylpropanoid (<strong>24</strong>), two phenolic glycosides (<strong>25</strong>–<strong>26</strong>), two aromatic glycosides (<strong>27</strong>–<strong>28</strong>), one phenolic (<strong>29</strong>), one lignan glycoside (<strong>30</strong>), one steroid glycoside (<strong>31</strong>), and one <span><span>fatty acid</span><svg><path></path></svg></span> (<strong>32</strong>). The structures of these isolated compounds were determined by analysis of their NMR spectroscopic (<sup>1</sup>H and <sup>13</sup>C) data and by comparison with previously reported data. Compounds <strong>4</strong> and <strong>8</strong>–<strong>10</strong> were first reported from <em>U. pumila</em>; compound <strong>12</strong> was obtained from the genus <em>Ulmus</em> for the first time, while compounds <strong>2</strong>, <strong>6</strong>, <strong>7</strong>, <strong>11</strong>, <strong>13</strong>, <strong>15</strong>–<strong>17</strong>, <strong>19</strong>–<strong>28</strong>, <strong>30</strong>, and <strong>32</strong> have never been isolated from the Ulmaceae family. Chemotaxonomic studies have shown that the genus <em>Ulmus</em> may be closely related to the genera <em>Hemiptelea</em>, <em>Zelkova</em>, and <em>Holoptelea</em>.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"117 ","pages":"Article 104907"},"PeriodicalIF":1.4000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chemical constituents of Ulmus pumila L. and their chemotaxonomic significance\",\"authors\":\"Deri Hu , Zhenyu Liu , Yue Yu , Chenghao Wu , Jinze Liu , Dongzhou Kang , Junzhe Min , Mingshan Zheng\",\"doi\":\"10.1016/j.bse.2024.104907\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A phytochemical study of the leaves of <em>Ulmus pumila</em> L. led to the isolation of 32 compounds, including fourteen flavonoids, which include flavonols (<strong>1</strong>–<strong>6</strong>), dihydroflavones (<strong>7</strong>–<strong>11</strong>), and dihydroflavonols (<strong>12</strong>–<strong>14</strong>), five terpenoids, which include megastigmane glycosides (<strong>15</strong>–<strong>17</strong>) and triterpenoids (<strong>18</strong>–<strong>19</strong>), four sugars (<strong>20</strong>–<strong>23</strong>), one phenylpropanoid (<strong>24</strong>), two phenolic glycosides (<strong>25</strong>–<strong>26</strong>), two aromatic glycosides (<strong>27</strong>–<strong>28</strong>), one phenolic (<strong>29</strong>), one lignan glycoside (<strong>30</strong>), one steroid glycoside (<strong>31</strong>), and one <span><span>fatty acid</span><svg><path></path></svg></span> (<strong>32</strong>). The structures of these isolated compounds were determined by analysis of their NMR spectroscopic (<sup>1</sup>H and <sup>13</sup>C) data and by comparison with previously reported data. Compounds <strong>4</strong> and <strong>8</strong>–<strong>10</strong> were first reported from <em>U. pumila</em>; compound <strong>12</strong> was obtained from the genus <em>Ulmus</em> for the first time, while compounds <strong>2</strong>, <strong>6</strong>, <strong>7</strong>, <strong>11</strong>, <strong>13</strong>, <strong>15</strong>–<strong>17</strong>, <strong>19</strong>–<strong>28</strong>, <strong>30</strong>, and <strong>32</strong> have never been isolated from the Ulmaceae family. Chemotaxonomic studies have shown that the genus <em>Ulmus</em> may be closely related to the genera <em>Hemiptelea</em>, <em>Zelkova</em>, and <em>Holoptelea</em>.</div></div>\",\"PeriodicalId\":8799,\"journal\":{\"name\":\"Biochemical Systematics and Ecology\",\"volume\":\"117 \",\"pages\":\"Article 104907\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-10-04\",\"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/S030519782400125X\",\"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/S030519782400125X","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}
Chemical constituents of Ulmus pumila L. and their chemotaxonomic significance
A phytochemical study of the leaves of Ulmus pumila L. led to the isolation of 32 compounds, including fourteen flavonoids, which include flavonols (1–6), dihydroflavones (7–11), and dihydroflavonols (12–14), five terpenoids, which include megastigmane glycosides (15–17) and triterpenoids (18–19), four sugars (20–23), one phenylpropanoid (24), two phenolic glycosides (25–26), two aromatic glycosides (27–28), one phenolic (29), one lignan glycoside (30), one steroid glycoside (31), and one fatty acid (32). The structures of these isolated compounds were determined by analysis of their NMR spectroscopic (1H and 13C) data and by comparison with previously reported data. Compounds 4 and 8–10 were first reported from U. pumila; compound 12 was obtained from the genus Ulmus for the first time, while compounds 2, 6, 7, 11, 13, 15–17, 19–28, 30, and 32 have never been isolated from the Ulmaceae family. Chemotaxonomic studies have shown that the genus Ulmus may be closely related to the genera Hemiptelea, Zelkova, and Holoptelea.
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.