Yue-Yao Li , Fei-Hua Yao , Qian Han , Jin-Li Luo , Xin-Yue Li , Cheng-Hai Gao , Xiang-Xi Yi
{"title":"海藻土中化学成分的化学分类意义","authors":"Yue-Yao Li , Fei-Hua Yao , Qian Han , Jin-Li Luo , Xin-Yue Li , Cheng-Hai Gao , Xiang-Xi Yi","doi":"10.1016/j.bse.2025.105024","DOIUrl":null,"url":null,"abstract":"<div><div>Chemical investigation of <em>Ligia exotica</em> resulted in the isolation of 15 compounds, including one cyclic tripeptide (<strong>1</strong>), eight cyclic dipeptides (<strong>2</strong>–<strong>8)</strong>, four alkaloids (<strong>9</strong>–<strong>12</strong>), two amino acids (<strong>13</strong>–<strong>14)</strong> and a <em>p</em>-hydroxy benzaldehyde (<strong>15</strong>). Their structures were identified by NMR spectroscopic data and comparison with previously reported data. Compounds <strong>1</strong>–<strong>2</strong>, and <strong>10–11</strong> were identified from the sea slater for the first time, and five compounds (<strong>1</strong>, <strong>2</strong>,<strong>10–12</strong>) have not previously been isolated from the genus <em>Ligia</em> and the family <em>Ligiidae</em>. Compound <strong>1</strong> exhibited potent anti-prostate cancer activity against 22Rv1 and PC-3 cells. This study also discussed the chemotaxonomic significance of these isolated compounds.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"122 ","pages":"Article 105024"},"PeriodicalIF":1.4000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chemotaxonomic significance of chemical constituents from Ligia exotica, sea slater\",\"authors\":\"Yue-Yao Li , Fei-Hua Yao , Qian Han , Jin-Li Luo , Xin-Yue Li , Cheng-Hai Gao , Xiang-Xi Yi\",\"doi\":\"10.1016/j.bse.2025.105024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Chemical investigation of <em>Ligia exotica</em> resulted in the isolation of 15 compounds, including one cyclic tripeptide (<strong>1</strong>), eight cyclic dipeptides (<strong>2</strong>–<strong>8)</strong>, four alkaloids (<strong>9</strong>–<strong>12</strong>), two amino acids (<strong>13</strong>–<strong>14)</strong> and a <em>p</em>-hydroxy benzaldehyde (<strong>15</strong>). Their structures were identified by NMR spectroscopic data and comparison with previously reported data. Compounds <strong>1</strong>–<strong>2</strong>, and <strong>10–11</strong> were identified from the sea slater for the first time, and five compounds (<strong>1</strong>, <strong>2</strong>,<strong>10–12</strong>) have not previously been isolated from the genus <em>Ligia</em> and the family <em>Ligiidae</em>. Compound <strong>1</strong> exhibited potent anti-prostate cancer activity against 22Rv1 and PC-3 cells. This study also discussed the chemotaxonomic significance of these isolated compounds.</div></div>\",\"PeriodicalId\":8799,\"journal\":{\"name\":\"Biochemical Systematics and Ecology\",\"volume\":\"122 \",\"pages\":\"Article 105024\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-04-22\",\"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/S0305197825000730\",\"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/S0305197825000730","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}
Chemotaxonomic significance of chemical constituents from Ligia exotica, sea slater
Chemical investigation of Ligia exotica resulted in the isolation of 15 compounds, including one cyclic tripeptide (1), eight cyclic dipeptides (2–8), four alkaloids (9–12), two amino acids (13–14) and a p-hydroxy benzaldehyde (15). Their structures were identified by NMR spectroscopic data and comparison with previously reported data. Compounds 1–2, and 10–11 were identified from the sea slater for the first time, and five compounds (1, 2,10–12) have not previously been isolated from the genus Ligia and the family Ligiidae. Compound 1 exhibited potent anti-prostate cancer activity against 22Rv1 and PC-3 cells. This study also discussed the chemotaxonomic significance of these isolated compounds.
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.