Thiago Araújo de Medeiros Brito, Ana Carolina Ferreira de Albuquerque, Fernando Martins Dos Santos Junior, Paulo Bruno Araújo Loureiro, Francisco Allysson Assis Ferreira Gadelha, Marianna Vieira Sobral, Domingos Benício Oliveira Silva Cardoso, Eudes da Silva Velozo, Josean Fechine Tavares, Lucas Silva Abreu, Marcelo Sobral da Silva
{"title":"梅特尼根木质素胺类化合物及其抗炎活性研究。","authors":"Thiago Araújo de Medeiros Brito, Ana Carolina Ferreira de Albuquerque, Fernando Martins Dos Santos Junior, Paulo Bruno Araújo Loureiro, Francisco Allysson Assis Ferreira Gadelha, Marianna Vieira Sobral, Domingos Benício Oliveira Silva Cardoso, Eudes da Silva Velozo, Josean Fechine Tavares, Lucas Silva Abreu, Marcelo Sobral da Silva","doi":"10.1021/acsomega.4c07336","DOIUrl":null,"url":null,"abstract":"<p><p>Five new lignanamides (<b>1</b>-<b>5</b>) and ten known amides (<b>6</b>-<b>15</b>) were isolated from the chloroform extract of <i>Metternichia macrocalyx</i> roots. The structures of the new compounds were elucidated via analysis of NMR spectroscopic and mass spectrometry data and known structures by comparison with data from the literature. Compound <b>1</b> had its absolute configuration established through ECD experiments, NMR calculations and quantum mechanical calculations. The anti-inflammatory activity of compounds (<b>1</b>-<b>5</b>) was assessed on RAW 264.7 macrophages. All the tested compounds reduced nitric oxide levels. In the cytokine quantification assays, only compound <b>2</b> did not significantly reduce IL-10 levels. Moreover, compounds <b>1</b>-<b>3</b> and <b>5</b> also reduced IL-1β levels. These results suggest the anti-inflammatory potential of these compounds.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"9 47","pages":"47065-47076"},"PeriodicalIF":4.3000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11603264/pdf/","citationCount":"0","resultStr":"{\"title\":\"Lignanamides from the Roots of <i>Metternichia macrocalyx</i> and Their Anti-inflammatory Activity.\",\"authors\":\"Thiago Araújo de Medeiros Brito, Ana Carolina Ferreira de Albuquerque, Fernando Martins Dos Santos Junior, Paulo Bruno Araújo Loureiro, Francisco Allysson Assis Ferreira Gadelha, Marianna Vieira Sobral, Domingos Benício Oliveira Silva Cardoso, Eudes da Silva Velozo, Josean Fechine Tavares, Lucas Silva Abreu, Marcelo Sobral da Silva\",\"doi\":\"10.1021/acsomega.4c07336\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Five new lignanamides (<b>1</b>-<b>5</b>) and ten known amides (<b>6</b>-<b>15</b>) were isolated from the chloroform extract of <i>Metternichia macrocalyx</i> roots. The structures of the new compounds were elucidated via analysis of NMR spectroscopic and mass spectrometry data and known structures by comparison with data from the literature. Compound <b>1</b> had its absolute configuration established through ECD experiments, NMR calculations and quantum mechanical calculations. The anti-inflammatory activity of compounds (<b>1</b>-<b>5</b>) was assessed on RAW 264.7 macrophages. All the tested compounds reduced nitric oxide levels. In the cytokine quantification assays, only compound <b>2</b> did not significantly reduce IL-10 levels. Moreover, compounds <b>1</b>-<b>3</b> and <b>5</b> also reduced IL-1β levels. These results suggest the anti-inflammatory potential of these compounds.</p>\",\"PeriodicalId\":22,\"journal\":{\"name\":\"ACS Omega\",\"volume\":\"9 47\",\"pages\":\"47065-47076\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11603264/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Omega\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acsomega.4c07336\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/26 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsomega.4c07336","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/26 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Lignanamides from the Roots of Metternichia macrocalyx and Their Anti-inflammatory Activity.
Five new lignanamides (1-5) and ten known amides (6-15) were isolated from the chloroform extract of Metternichia macrocalyx roots. The structures of the new compounds were elucidated via analysis of NMR spectroscopic and mass spectrometry data and known structures by comparison with data from the literature. Compound 1 had its absolute configuration established through ECD experiments, NMR calculations and quantum mechanical calculations. The anti-inflammatory activity of compounds (1-5) was assessed on RAW 264.7 macrophages. All the tested compounds reduced nitric oxide levels. In the cytokine quantification assays, only compound 2 did not significantly reduce IL-10 levels. Moreover, compounds 1-3 and 5 also reduced IL-1β levels. These results suggest the anti-inflammatory potential of these compounds.
ACS OmegaChemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍:
ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.