Mohamed Ibrahim Badaoui , Sonia Chabani , Abdulmagid Alabdul Magid , Laurence Voutquenne-Nazabadioko , Charlotte Sayagh , Dominique Harakat , Hamada Haba
{"title":"Chemical constituents of Centaurea dissecta Ten. and sesquiterpenes chemotaxonomic significance","authors":"Mohamed Ibrahim Badaoui , Sonia Chabani , Abdulmagid Alabdul Magid , Laurence Voutquenne-Nazabadioko , Charlotte Sayagh , Dominique Harakat , Hamada Haba","doi":"10.1016/j.bse.2024.104808","DOIUrl":null,"url":null,"abstract":"<div><p>The phytochemical investigation of <em>Centaurea dissecta</em> Ten. led to the isolation of thirty-two compounds of diverse chemical classes including two sesquiterpene lactones (<strong>1</strong>, <strong>2</strong>), two sesquiterpenes (<strong>3</strong>, <strong>4</strong>), twelve flavonoids (<strong>5</strong>–<strong>16</strong>), one lignan (<strong>17</strong>), twelve phenols (<strong>18</strong>–<strong>29</strong>), one triterpene (<strong>30</strong>) and two phytosterols (<strong>31</strong>, <strong>32</strong>) from the EtOAc and <em>n</em>-BuOH soluble fractions of the 70% aqueous ethanol extract. Furthermore, the phenolic and flavonoid contents were measured for the petroleum ether, EtOAc and <em>n</em>-BuOH soluble fractions. The chemical structures of these compounds were determined by using a combination of NMR spectroscopic and mass spectrometry (ESI-MS) analyses, as well as by comparison with literature values. Only apigenin (<strong>15</strong>) was isolated previously from <em>Centaurea affinis</em>, and all other compounds were isolated for the first time from this species. Noticeably, ethyl ferulate (<strong>20</strong>), ethyl caffeate (<strong>21</strong>), synapyl aldehyde (<strong>22</strong>), coniferyl aldehyde (<strong>23</strong>), 2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone (<strong>24</strong>), and <em>C</em>-veratroylglycol (<strong>25</strong>), have not been reported from the genus <em>Centaurea</em>. All compounds have been previously isolated in various plants belonging to the Asteraceae family. Meanwhile, the chemotaxonomic significance of the isolated compounds was summarized.</p></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2024-03-06","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/S0305197824000267","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: 0
Abstract
The phytochemical investigation of Centaurea dissecta Ten. led to the isolation of thirty-two compounds of diverse chemical classes including two sesquiterpene lactones (1, 2), two sesquiterpenes (3, 4), twelve flavonoids (5–16), one lignan (17), twelve phenols (18–29), one triterpene (30) and two phytosterols (31, 32) from the EtOAc and n-BuOH soluble fractions of the 70% aqueous ethanol extract. Furthermore, the phenolic and flavonoid contents were measured for the petroleum ether, EtOAc and n-BuOH soluble fractions. The chemical structures of these compounds were determined by using a combination of NMR spectroscopic and mass spectrometry (ESI-MS) analyses, as well as by comparison with literature values. Only apigenin (15) was isolated previously from Centaurea affinis, and all other compounds were isolated for the first time from this species. Noticeably, ethyl ferulate (20), ethyl caffeate (21), synapyl aldehyde (22), coniferyl aldehyde (23), 2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone (24), and C-veratroylglycol (25), have not been reported from the genus Centaurea. All compounds have been previously isolated in various plants belonging to the Asteraceae family. Meanwhile, the chemotaxonomic significance of the isolated compounds was summarized.
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.