Ervira Keubou Djoukam , Roukayatou Mbouangouere , Jean-De-Dieu Tamokou , Arno R. Donfack Nanfack , Germaine Matsuete-Takongmo , Apollinaire Tsopmo , Mathieu Tene
{"title":"A new antibacterial diarylpropanoid and other constituents from Lannea velutina A. Rich (Anacardiaceae) and their chemotaxonomic significance","authors":"Ervira Keubou Djoukam , Roukayatou Mbouangouere , Jean-De-Dieu Tamokou , Arno R. Donfack Nanfack , Germaine Matsuete-Takongmo , Apollinaire Tsopmo , Mathieu Tene","doi":"10.1016/j.bse.2025.105063","DOIUrl":null,"url":null,"abstract":"<div><div>Phytochemical investigation of the methanol extracts from the stem bark and leaves of <em>Lannea velutina</em> afforded a new diarylpropanoid (<strong>1</strong>) and eighteen previously described compounds from other plants. They included eleven flavonoids (<strong>2</strong>–<strong>12</strong>), three triterpenoids (<strong>13</strong>–<strong>15</strong>), three steroids (<strong>16</strong>–<strong>18</strong>) and one sugar (<strong>19</strong>). The structure of compound <strong>1</strong> was established by analysis of its spectroscopic and spectrometric data. All the isolated compounds are here reported for the first time from <em>L. velutina</em> species while only compounds <strong>3</strong>, <strong>6</strong>, <strong>8</strong>, <strong>10</strong>, <strong>13</strong>–<strong>16</strong> and <strong>18</strong> were previously reported from the genus <em>Lannea</em>. The extracts, fractions, and compounds were subjected to <em>in vitro</em> antibacterial assays against one Gram-positive (<em>Enterococcus faecalis</em> ATCC 29212) and three Gram-negative (<em>Escherichia coli</em> ATCC 8739, <em>Salmonella</em> Typhi ATCC 6539 and <em>Pseudomonas aeruginosa</em> 4C 76110) bacteria. The MeOH extract from the stem bark, its chromatographic fraction C and the EtOAc partitioned leaves extract showed significant activity against the growth of <em>E. faecalis</em>, <em>E. coli</em> and <em>P. aeruginosa</em> (16 ≤ MIC ≤64 μg/mL). Lannepoxide (<strong>1</strong>) inhibition activities were 16 ≤ MIC ≤128 μg/mL against the four bacterial strains. The findings demonstrated the chemotaxonomic significance of the isolated compounds and their potential as antimicrobial agents.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"123 ","pages":"Article 105063"},"PeriodicalIF":1.4000,"publicationDate":"2025-06-16","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/S0305197825001127","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
Phytochemical investigation of the methanol extracts from the stem bark and leaves of Lannea velutina afforded a new diarylpropanoid (1) and eighteen previously described compounds from other plants. They included eleven flavonoids (2–12), three triterpenoids (13–15), three steroids (16–18) and one sugar (19). The structure of compound 1 was established by analysis of its spectroscopic and spectrometric data. All the isolated compounds are here reported for the first time from L. velutina species while only compounds 3, 6, 8, 10, 13–16 and 18 were previously reported from the genus Lannea. The extracts, fractions, and compounds were subjected to in vitro antibacterial assays against one Gram-positive (Enterococcus faecalis ATCC 29212) and three Gram-negative (Escherichia coli ATCC 8739, Salmonella Typhi ATCC 6539 and Pseudomonas aeruginosa 4C 76110) bacteria. The MeOH extract from the stem bark, its chromatographic fraction C and the EtOAc partitioned leaves extract showed significant activity against the growth of E. faecalis, E. coli and P. aeruginosa (16 ≤ MIC ≤64 μg/mL). Lannepoxide (1) inhibition activities were 16 ≤ MIC ≤128 μg/mL against the four bacterial strains. The findings demonstrated the chemotaxonomic significance of the isolated compounds and their potential as antimicrobial agents.
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.