{"title":"雪松中的 8',9'-双新木质素及其抗血管生成活性","authors":"Valeria Iobbi , Shiva Pouramin Arabi , Angela Bisio , Valeria D’Angelo , Maria Paola Germanò , Alessandra Braca , Nunziatina De Tommasi","doi":"10.1016/j.phytol.2024.09.002","DOIUrl":null,"url":null,"abstract":"<div><div>Two previously undescribed 8’,9’-bis-<em>nor</em>-neolignans, 9-acetyltoonin C (<strong>1</strong>) and <em>threo</em>-guaiacylglycerol-β-methyl vanillate ether (<strong>2</strong>), were isolated from the stem bark of <em>Cedrela odorata</em> (Meliaceae), together with 4,5-dihydroblumenol A, 2-(3,4-dimethoxyphenyl)ethyl-β-<span>d</span>-glucopyranoside, scopoletin, homovanillic alcohol, and 7-megastigmene-3,6,9-triol. All compounds were characterized by 1D and 2D NMR and HRESIMS data. The new compounds and other lignans obtained from our chemical library, namely <em>erythro</em>-4,7,9,9’-tetrahydroxy-3,3’-dimethoxy-8-<em>O</em>-4’-oxyneolignan (<strong>3</strong>), urolignoside (<strong>4</strong>), secoisolariciresinol 9-<em>O</em>-β-D-glucopyranoside (<strong>5</strong>), icariside E<sub>3</sub>, and <em>erythro</em>-4,7,9,9’-tetrahydroxy-3,3’-dimethoxy-8-<em>O</em>-4’-oxyneolignan-9’-<em>O</em>-β-D-glucopyranoside, were then evaluated for their antiangiogenic activity by the <em>in vivo</em> zebrafish embryos test. Compounds <strong>1</strong>, <strong>2</strong>, and <strong>3</strong> exhibited the best antiangiogenic response, while <strong>4</strong> and <strong>5</strong> showed mild inhibitory effects on EAP release after treatment of zebrafish embryos. In particular, compound <strong>2</strong> induced an inhibition of 42.56 % at 10 μM, similarly to 2-methoxyestradiol used as reference compound.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"64 ","pages":"Pages 13-18"},"PeriodicalIF":1.3000,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"8’,9’-Bis-nor-neolignans from Cedrela odorata and their antiangiogenic activity\",\"authors\":\"Valeria Iobbi , Shiva Pouramin Arabi , Angela Bisio , Valeria D’Angelo , Maria Paola Germanò , Alessandra Braca , Nunziatina De Tommasi\",\"doi\":\"10.1016/j.phytol.2024.09.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Two previously undescribed 8’,9’-bis-<em>nor</em>-neolignans, 9-acetyltoonin C (<strong>1</strong>) and <em>threo</em>-guaiacylglycerol-β-methyl vanillate ether (<strong>2</strong>), were isolated from the stem bark of <em>Cedrela odorata</em> (Meliaceae), together with 4,5-dihydroblumenol A, 2-(3,4-dimethoxyphenyl)ethyl-β-<span>d</span>-glucopyranoside, scopoletin, homovanillic alcohol, and 7-megastigmene-3,6,9-triol. All compounds were characterized by 1D and 2D NMR and HRESIMS data. The new compounds and other lignans obtained from our chemical library, namely <em>erythro</em>-4,7,9,9’-tetrahydroxy-3,3’-dimethoxy-8-<em>O</em>-4’-oxyneolignan (<strong>3</strong>), urolignoside (<strong>4</strong>), secoisolariciresinol 9-<em>O</em>-β-D-glucopyranoside (<strong>5</strong>), icariside E<sub>3</sub>, and <em>erythro</em>-4,7,9,9’-tetrahydroxy-3,3’-dimethoxy-8-<em>O</em>-4’-oxyneolignan-9’-<em>O</em>-β-D-glucopyranoside, were then evaluated for their antiangiogenic activity by the <em>in vivo</em> zebrafish embryos test. Compounds <strong>1</strong>, <strong>2</strong>, and <strong>3</strong> exhibited the best antiangiogenic response, while <strong>4</strong> and <strong>5</strong> showed mild inhibitory effects on EAP release after treatment of zebrafish embryos. In particular, compound <strong>2</strong> induced an inhibition of 42.56 % at 10 μM, similarly to 2-methoxyestradiol used as reference compound.</div></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"64 \",\"pages\":\"Pages 13-18\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry Letters\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1874390024001319\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1874390024001319","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
8’,9’-Bis-nor-neolignans from Cedrela odorata and their antiangiogenic activity
Two previously undescribed 8’,9’-bis-nor-neolignans, 9-acetyltoonin C (1) and threo-guaiacylglycerol-β-methyl vanillate ether (2), were isolated from the stem bark of Cedrela odorata (Meliaceae), together with 4,5-dihydroblumenol A, 2-(3,4-dimethoxyphenyl)ethyl-β-d-glucopyranoside, scopoletin, homovanillic alcohol, and 7-megastigmene-3,6,9-triol. All compounds were characterized by 1D and 2D NMR and HRESIMS data. The new compounds and other lignans obtained from our chemical library, namely erythro-4,7,9,9’-tetrahydroxy-3,3’-dimethoxy-8-O-4’-oxyneolignan (3), urolignoside (4), secoisolariciresinol 9-O-β-D-glucopyranoside (5), icariside E3, and erythro-4,7,9,9’-tetrahydroxy-3,3’-dimethoxy-8-O-4’-oxyneolignan-9’-O-β-D-glucopyranoside, were then evaluated for their antiangiogenic activity by the in vivo zebrafish embryos test. Compounds 1, 2, and 3 exhibited the best antiangiogenic response, while 4 and 5 showed mild inhibitory effects on EAP release after treatment of zebrafish embryos. In particular, compound 2 induced an inhibition of 42.56 % at 10 μM, similarly to 2-methoxyestradiol used as reference compound.
期刊介绍:
Phytochemistry Letters invites rapid communications on all aspects of natural product research including:
• Structural elucidation of natural products
• Analytical evaluation of herbal medicines
• Clinical efficacy, safety and pharmacovigilance of herbal medicines
• Natural product biosynthesis
• Natural product synthesis and chemical modification
• Natural product metabolism
• Chemical ecology
• Biotechnology
• Bioassay-guided isolation
• Pharmacognosy
• Pharmacology of natural products
• Metabolomics
• Ethnobotany and traditional usage
• Genetics of natural products
Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.