{"title":"椭圆肉豆蔻抗氧化和抗炎成分的研究","authors":"Chih-Hui Chin, Zih-Rong Chen, Tsung-Hsien Chang, Chia-Ching Liaw, Ping-Jyun Sung, Ming-Jen Cheng, Chien-Ming Huang, Jih-Jung Chen","doi":"10.1007/s10600-025-04568-8","DOIUrl":null,"url":null,"abstract":"<p>A new neolignan derivative, myrisellipin (<b>1</b>), has been isolated from the seeds of <i>Myristica elliptica</i> var. simiarum, together with seven known compounds, licarin A (<b>2</b>), accuminatin (<b>3</b>), butein (<b>4</b>), 3′-hydroxypterostilbene (<b>5</b>), malabaricone B (<b>6</b>), malabaricone C (<b>7</b>), and 3-(3,4,5-trimethoxyphenyl)-2-(E)-propen-1-ol (<b>8</b>). The structure of new compound <b>1</b> was determined through spectroscopic and MS analyses. Among the isolated compounds, <b>1</b>, <b>4</b>, <b>5</b>, <b>7</b>, <b>8</b> showed potent inhibition, with IC<sub>50</sub> values of 16.83 ± 1.18, 17.92 ± 1.28, 25.06 ± 2.01, 22.05 ± 1.74, and 23.58 ± 1.96 μM respectively, against LPS-induced NO generation. In addition, compounds <b>4</b>, <b>5</b>, and <b>8</b> also showed potent DPPH radical scavenging activities, with IC<sub>50</sub> values of 37.02 ± 2.89, 80.36 ± 5.78, and 50.07 ± 4.11 μM, respectively.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 1","pages":"27 - 31"},"PeriodicalIF":0.8000,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antioxidant and Anti-Inflammatory Constituents from Myristica elliptica var. simiarum\",\"authors\":\"Chih-Hui Chin, Zih-Rong Chen, Tsung-Hsien Chang, Chia-Ching Liaw, Ping-Jyun Sung, Ming-Jen Cheng, Chien-Ming Huang, Jih-Jung Chen\",\"doi\":\"10.1007/s10600-025-04568-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A new neolignan derivative, myrisellipin (<b>1</b>), has been isolated from the seeds of <i>Myristica elliptica</i> var. simiarum, together with seven known compounds, licarin A (<b>2</b>), accuminatin (<b>3</b>), butein (<b>4</b>), 3′-hydroxypterostilbene (<b>5</b>), malabaricone B (<b>6</b>), malabaricone C (<b>7</b>), and 3-(3,4,5-trimethoxyphenyl)-2-(E)-propen-1-ol (<b>8</b>). The structure of new compound <b>1</b> was determined through spectroscopic and MS analyses. Among the isolated compounds, <b>1</b>, <b>4</b>, <b>5</b>, <b>7</b>, <b>8</b> showed potent inhibition, with IC<sub>50</sub> values of 16.83 ± 1.18, 17.92 ± 1.28, 25.06 ± 2.01, 22.05 ± 1.74, and 23.58 ± 1.96 μM respectively, against LPS-induced NO generation. In addition, compounds <b>4</b>, <b>5</b>, and <b>8</b> also showed potent DPPH radical scavenging activities, with IC<sub>50</sub> values of 37.02 ± 2.89, 80.36 ± 5.78, and 50.07 ± 4.11 μM, respectively.</p>\",\"PeriodicalId\":514,\"journal\":{\"name\":\"Chemistry of Natural Compounds\",\"volume\":\"61 1\",\"pages\":\"27 - 31\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-02-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Natural Compounds\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10600-025-04568-8\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04568-8","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Antioxidant and Anti-Inflammatory Constituents from Myristica elliptica var. simiarum
A new neolignan derivative, myrisellipin (1), has been isolated from the seeds of Myristica elliptica var. simiarum, together with seven known compounds, licarin A (2), accuminatin (3), butein (4), 3′-hydroxypterostilbene (5), malabaricone B (6), malabaricone C (7), and 3-(3,4,5-trimethoxyphenyl)-2-(E)-propen-1-ol (8). The structure of new compound 1 was determined through spectroscopic and MS analyses. Among the isolated compounds, 1, 4, 5, 7, 8 showed potent inhibition, with IC50 values of 16.83 ± 1.18, 17.92 ± 1.28, 25.06 ± 2.01, 22.05 ± 1.74, and 23.58 ± 1.96 μM respectively, against LPS-induced NO generation. In addition, compounds 4, 5, and 8 also showed potent DPPH radical scavenging activities, with IC50 values of 37.02 ± 2.89, 80.36 ± 5.78, and 50.07 ± 4.11 μM, respectively.
期刊介绍:
Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.