Lisset Ortiz-Zamora, Jaderson V Ferreira, Nayana K S de Oliveira, Fábio A de Molfetta, Lorane I S Hage-Melim, Caio P Fernandes, Anna E M F M Oliveira
{"title":"对杀虫活性的潜在影响:一项硅研究。","authors":"Lisset Ortiz-Zamora, Jaderson V Ferreira, Nayana K S de Oliveira, Fábio A de Molfetta, Lorane I S Hage-Melim, Caio P Fernandes, Anna E M F M Oliveira","doi":"10.2174/1872208316666220106110902","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>From the fruits and seeds of the species of Pterodon, it is possible to obtain two main products: essential oil and oleoresin. In oleoresin, numerous vouacapan compounds have been demonstrated to have biological potential, including insecticidal activity.</p><p><strong>Objective: </strong>In silico studies were performed to identify potential candidates for natural insecticides among the vouacapans present in the genus Pterodon.</p><p><strong>Materials and methods: </strong>Molecular docking and molecular dynamics studies were performed to analyze the interaction of vouacapan compounds with acetylcholinesterase of Drosophila melanogaster. Pharmacokinetic parameters regarding physicochemical properties, plasma protein binding, and activity in the central nervous system were evaluated. The toxicological properties of the selected molecules were predicted using malathion as the reference compound.</p><p><strong>Results: </strong>6α,7β-dimethoxivouacapan-17-ene (15) showed a high number of interactions and scores in molecular docking studies. These results suggested that this compound exhibits an inhibitory activity of the enzyme acetylcholinesterase. This compound showed the best results regarding physicochemical properties, besides presenting low cutaneous permeability values, suggesting null absorption. Molecular dynamics studies demonstrated few conformational changes in the structure of the complex formed by compound 4 and acetylcholinesterase enzyme throughout the simulation time.</p><p><strong>Conclusion: </strong>It was determined that compound 4 (vouacapan 6α,7β,17β,19-tetraol) could be an excellent candidate for usage as a natural insecticide.</p>","PeriodicalId":21064,"journal":{"name":"Recent patents on biotechnology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Potential Implications of Vouacapan Compounds for Insecticidal Activity: An In Silico Study.\",\"authors\":\"Lisset Ortiz-Zamora, Jaderson V Ferreira, Nayana K S de Oliveira, Fábio A de Molfetta, Lorane I S Hage-Melim, Caio P Fernandes, Anna E M F M Oliveira\",\"doi\":\"10.2174/1872208316666220106110902\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>From the fruits and seeds of the species of Pterodon, it is possible to obtain two main products: essential oil and oleoresin. In oleoresin, numerous vouacapan compounds have been demonstrated to have biological potential, including insecticidal activity.</p><p><strong>Objective: </strong>In silico studies were performed to identify potential candidates for natural insecticides among the vouacapans present in the genus Pterodon.</p><p><strong>Materials and methods: </strong>Molecular docking and molecular dynamics studies were performed to analyze the interaction of vouacapan compounds with acetylcholinesterase of Drosophila melanogaster. Pharmacokinetic parameters regarding physicochemical properties, plasma protein binding, and activity in the central nervous system were evaluated. The toxicological properties of the selected molecules were predicted using malathion as the reference compound.</p><p><strong>Results: </strong>6α,7β-dimethoxivouacapan-17-ene (15) showed a high number of interactions and scores in molecular docking studies. These results suggested that this compound exhibits an inhibitory activity of the enzyme acetylcholinesterase. This compound showed the best results regarding physicochemical properties, besides presenting low cutaneous permeability values, suggesting null absorption. Molecular dynamics studies demonstrated few conformational changes in the structure of the complex formed by compound 4 and acetylcholinesterase enzyme throughout the simulation time.</p><p><strong>Conclusion: </strong>It was determined that compound 4 (vouacapan 6α,7β,17β,19-tetraol) could be an excellent candidate for usage as a natural insecticide.</p>\",\"PeriodicalId\":21064,\"journal\":{\"name\":\"Recent patents on biotechnology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Recent patents on biotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/1872208316666220106110902\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Recent patents on biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1872208316666220106110902","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
Potential Implications of Vouacapan Compounds for Insecticidal Activity: An In Silico Study.
Background: From the fruits and seeds of the species of Pterodon, it is possible to obtain two main products: essential oil and oleoresin. In oleoresin, numerous vouacapan compounds have been demonstrated to have biological potential, including insecticidal activity.
Objective: In silico studies were performed to identify potential candidates for natural insecticides among the vouacapans present in the genus Pterodon.
Materials and methods: Molecular docking and molecular dynamics studies were performed to analyze the interaction of vouacapan compounds with acetylcholinesterase of Drosophila melanogaster. Pharmacokinetic parameters regarding physicochemical properties, plasma protein binding, and activity in the central nervous system were evaluated. The toxicological properties of the selected molecules were predicted using malathion as the reference compound.
Results: 6α,7β-dimethoxivouacapan-17-ene (15) showed a high number of interactions and scores in molecular docking studies. These results suggested that this compound exhibits an inhibitory activity of the enzyme acetylcholinesterase. This compound showed the best results regarding physicochemical properties, besides presenting low cutaneous permeability values, suggesting null absorption. Molecular dynamics studies demonstrated few conformational changes in the structure of the complex formed by compound 4 and acetylcholinesterase enzyme throughout the simulation time.
Conclusion: It was determined that compound 4 (vouacapan 6α,7β,17β,19-tetraol) could be an excellent candidate for usage as a natural insecticide.
期刊介绍:
Recent Patents on Biotechnology publishes review articles by experts on recent patents on biotechnology. A selection of important and recent patents on biotechnology is also included in the journal. The journal is essential reading for all researchers involved in all fields of biotechnology.