Nurul Najihah Husna Tanazi, Ahmad Nazif Aziz, Mohamad Nurul Azmi, Mohamad Hafizi Abu Bakar, Muhamad Fairus Noor Hassim, Nurul Huda Abdul Wahab, Nurulfazlina Edayah Rasol, Nurunajah Ab Ghani, M Maulidiani, Khalijah Awang
{"title":"金缕莲的植物成分研究-淀粉酶和-葡萄糖苷酶的降糖作用及分子对接研究。","authors":"Nurul Najihah Husna Tanazi, Ahmad Nazif Aziz, Mohamad Nurul Azmi, Mohamad Hafizi Abu Bakar, Muhamad Fairus Noor Hassim, Nurul Huda Abdul Wahab, Nurulfazlina Edayah Rasol, Nurunajah Ab Ghani, M Maulidiani, Khalijah Awang","doi":"10.1080/14786419.2023.2283759","DOIUrl":null,"url":null,"abstract":"<p><p>Phytochemical investigation on the bark of <i>E. kingiana</i> plant afforded ten compounds, including six polyketides namely kingianin A <b>1</b>, kingianin B <b>2</b>, kingianin E <b>3</b>, kingianin F <b>4</b>, kingianin K <b>5</b> and kingianin L <b>6</b>, three endiandric acids; kingianic acid A <b>7</b>, tsangibeilin B <b>8</b> and endiandric acid M <b>9</b>, and one sesquiterpene; daibuoxide <b>10</b>. All compounds were separated as racemic mixture by recycling high-performance liquid chromatography (RHPLC), except for daibuoxide. Their structures were elucidated by detailed spectroscopic and comparative literature data analysis. This is the first report on the presence of the sesquiterpene; daibuoxide in <i>Endiandra</i> genus. <i>In vitro</i> enzymatic bio-evaluation of the isolated compounds against <i>α</i>-amylase and <i>α</i>-glucosidase showed that <b>4</b> demonstrated the best <i>α</i>-amylase and <i>α</i>-glucosidase inhibitory activity with IC<sub>50</sub> values of 181.54 ± 6.27 µg/mL and 237.87 ± 0.07 µg/mL, respectively. In addition, molecular docking analysis confirmed the <i>α</i>-amylase and <i>α</i>-glucosidase inhibitory activities demonstrated by <b>4</b>.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"4375-4382"},"PeriodicalIF":1.9000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phytoconstituents of <i>Endiandra kingiana</i>; antidiabetic effects and molecular docking studies on alpha-amylase and alpha-glucosidase.\",\"authors\":\"Nurul Najihah Husna Tanazi, Ahmad Nazif Aziz, Mohamad Nurul Azmi, Mohamad Hafizi Abu Bakar, Muhamad Fairus Noor Hassim, Nurul Huda Abdul Wahab, Nurulfazlina Edayah Rasol, Nurunajah Ab Ghani, M Maulidiani, Khalijah Awang\",\"doi\":\"10.1080/14786419.2023.2283759\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Phytochemical investigation on the bark of <i>E. kingiana</i> plant afforded ten compounds, including six polyketides namely kingianin A <b>1</b>, kingianin B <b>2</b>, kingianin E <b>3</b>, kingianin F <b>4</b>, kingianin K <b>5</b> and kingianin L <b>6</b>, three endiandric acids; kingianic acid A <b>7</b>, tsangibeilin B <b>8</b> and endiandric acid M <b>9</b>, and one sesquiterpene; daibuoxide <b>10</b>. All compounds were separated as racemic mixture by recycling high-performance liquid chromatography (RHPLC), except for daibuoxide. Their structures were elucidated by detailed spectroscopic and comparative literature data analysis. This is the first report on the presence of the sesquiterpene; daibuoxide in <i>Endiandra</i> genus. <i>In vitro</i> enzymatic bio-evaluation of the isolated compounds against <i>α</i>-amylase and <i>α</i>-glucosidase showed that <b>4</b> demonstrated the best <i>α</i>-amylase and <i>α</i>-glucosidase inhibitory activity with IC<sub>50</sub> values of 181.54 ± 6.27 µg/mL and 237.87 ± 0.07 µg/mL, respectively. In addition, molecular docking analysis confirmed the <i>α</i>-amylase and <i>α</i>-glucosidase inhibitory activities demonstrated by <b>4</b>.</p>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\" \",\"pages\":\"4375-4382\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1080/14786419.2023.2283759\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/11/27 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2023.2283759","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/11/27 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Phytoconstituents of Endiandra kingiana; antidiabetic effects and molecular docking studies on alpha-amylase and alpha-glucosidase.
Phytochemical investigation on the bark of E. kingiana plant afforded ten compounds, including six polyketides namely kingianin A 1, kingianin B 2, kingianin E 3, kingianin F 4, kingianin K 5 and kingianin L 6, three endiandric acids; kingianic acid A 7, tsangibeilin B 8 and endiandric acid M 9, and one sesquiterpene; daibuoxide 10. All compounds were separated as racemic mixture by recycling high-performance liquid chromatography (RHPLC), except for daibuoxide. Their structures were elucidated by detailed spectroscopic and comparative literature data analysis. This is the first report on the presence of the sesquiterpene; daibuoxide in Endiandra genus. In vitro enzymatic bio-evaluation of the isolated compounds against α-amylase and α-glucosidase showed that 4 demonstrated the best α-amylase and α-glucosidase inhibitory activity with IC50 values of 181.54 ± 6.27 µg/mL and 237.87 ± 0.07 µg/mL, respectively. In addition, molecular docking analysis confirmed the α-amylase and α-glucosidase inhibitory activities demonstrated by 4.
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.