{"title":"柞蚕子木脂素和酚类苷类及其α-淀粉酶和α-葡萄糖苷酶抑制活性研究","authors":"Yi-Yuan Tang , Jia Chen , Hong-Juan Zhou , Wei Ji , Jian-Hua Shao , Feng-Min Zhang , Chun-Chao Zhao","doi":"10.1080/14786419.2023.2289084","DOIUrl":null,"url":null,"abstract":"<div><div>The phytochemical investigation on the methanol extract of <em>Viburnum betulifolium</em> fruits resulted in the isolation and identification of two new lignan constituents (<strong>1</strong> and <strong>2</strong>) and seven known phenolic glycosides (<strong>3</strong>–<strong>9</strong>). The structures of new isolates, including their absolute configurations were elucidated by extensive spectroscopic analyses (<sup>1</sup>H and <sup>13</sup>C NMR, HSQC, HMBC, HRESIMS, and ECD) and chemical methods. In the <em>in vitro</em> enzyme assays, compounds <strong>1</strong>, <strong>2</strong>, <strong>6</strong>, and <strong>8</strong> showed potential <em>α</em>‑amylase and <em>α</em>-glucosidase inhibitory activities. Among them, compound <strong>1</strong> exhibited stronger inhibitory effects towards <em>α</em>-amylase and <em>α</em>-glucosidase with the IC<sub>50</sub> values of 12.68 and 15.17 μM, respectively, than those of the positive control acarbose (IC<sub>50</sub>, 29.19 and 18.15 μM, respectively). In addition, the molecular docking analyses of compound <strong>1</strong> with strongest inhibition against the target enzymes were also performed.</div></div>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":"39 4","pages":"Pages 742-748"},"PeriodicalIF":1.9000,"publicationDate":"2025-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lignan and phenolic glycosides from Viburnum betulifolium fruits and their α‑amylase and α-glucosidase inhibitory activities\",\"authors\":\"Yi-Yuan Tang , Jia Chen , Hong-Juan Zhou , Wei Ji , Jian-Hua Shao , Feng-Min Zhang , Chun-Chao Zhao\",\"doi\":\"10.1080/14786419.2023.2289084\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The phytochemical investigation on the methanol extract of <em>Viburnum betulifolium</em> fruits resulted in the isolation and identification of two new lignan constituents (<strong>1</strong> and <strong>2</strong>) and seven known phenolic glycosides (<strong>3</strong>–<strong>9</strong>). The structures of new isolates, including their absolute configurations were elucidated by extensive spectroscopic analyses (<sup>1</sup>H and <sup>13</sup>C NMR, HSQC, HMBC, HRESIMS, and ECD) and chemical methods. In the <em>in vitro</em> enzyme assays, compounds <strong>1</strong>, <strong>2</strong>, <strong>6</strong>, and <strong>8</strong> showed potential <em>α</em>‑amylase and <em>α</em>-glucosidase inhibitory activities. Among them, compound <strong>1</strong> exhibited stronger inhibitory effects towards <em>α</em>-amylase and <em>α</em>-glucosidase with the IC<sub>50</sub> values of 12.68 and 15.17 μM, respectively, than those of the positive control acarbose (IC<sub>50</sub>, 29.19 and 18.15 μM, respectively). In addition, the molecular docking analyses of compound <strong>1</strong> with strongest inhibition against the target enzymes were also performed.</div></div>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\"39 4\",\"pages\":\"Pages 742-748\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-02-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1478641923024397\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1478641923024397","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Lignan and phenolic glycosides from Viburnum betulifolium fruits and their α‑amylase and α-glucosidase inhibitory activities
The phytochemical investigation on the methanol extract of Viburnum betulifolium fruits resulted in the isolation and identification of two new lignan constituents (1 and 2) and seven known phenolic glycosides (3–9). The structures of new isolates, including their absolute configurations were elucidated by extensive spectroscopic analyses (1H and 13C NMR, HSQC, HMBC, HRESIMS, and ECD) and chemical methods. In the in vitro enzyme assays, compounds 1, 2, 6, and 8 showed potential α‑amylase and α-glucosidase inhibitory activities. Among them, compound 1 exhibited stronger inhibitory effects towards α-amylase and α-glucosidase with the IC50 values of 12.68 and 15.17 μM, respectively, than those of the positive control acarbose (IC50, 29.19 and 18.15 μM, respectively). In addition, the molecular docking analyses of compound 1 with strongest inhibition against the target enzymes were also performed.
期刊介绍:
The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds.
The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal.
Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section.
All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.