Conformational characterization of ipomotaosides and their recognition by COX-1 and 2
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/267616 |
Resumo: | The aerial parts of Ipomoea batatas are described herein to produce four new resin glycosides, designated as ipomotaosides A, B, C, and D. Ipomotaoside A was found to present inhibitory activity on both cyclooxygenases. However, the conformational elucidation of these molecules may be difficult due to their high flexibility. In this context, the current work presents a conformational characterization of ipomotaosides A–D in aqueous and nonaqueous solvents. The employed protocol includes metadynamics evaluation and unrestrained molecular dynamics simulations (MD). The obtained data provided structural models for the ipomotaosides in good agreement with previous ROESY distances measured in pyridine. Accordingly, the most abundant conformation of ipomotaoside A in solution was employed in flexible docking studies, providing a structural basis for the compound’s inhibition of COX enzymes. The so-obtained complex supports resin glycosides’ role as original scaffolds for future studies, aiming at structural optimization and development of potential new anti-inflammatory agents. |
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Arantes, Pablo RicardoSachett, Liana GuimarãesGraebin, Cedric StephanVerli, Hugo2023-11-25T03:26:15Z20141420-3049http://hdl.handle.net/10183/267616000990958The aerial parts of Ipomoea batatas are described herein to produce four new resin glycosides, designated as ipomotaosides A, B, C, and D. Ipomotaoside A was found to present inhibitory activity on both cyclooxygenases. However, the conformational elucidation of these molecules may be difficult due to their high flexibility. In this context, the current work presents a conformational characterization of ipomotaosides A–D in aqueous and nonaqueous solvents. The employed protocol includes metadynamics evaluation and unrestrained molecular dynamics simulations (MD). The obtained data provided structural models for the ipomotaosides in good agreement with previous ROESY distances measured in pyridine. Accordingly, the most abundant conformation of ipomotaoside A in solution was employed in flexible docking studies, providing a structural basis for the compound’s inhibition of COX enzymes. The so-obtained complex supports resin glycosides’ role as original scaffolds for future studies, aiming at structural optimization and development of potential new anti-inflammatory agents.application/pdfengMolecules. Basel, SW. Vol. 19, no. 4 (2014), p. 5421-5433IpomotaosidesDinâmica molecularDissacarídeosIpomotaosidesResin glycosidesDisaccharidesMolecular dynamicsDockingInflammatory processConformational characterization of ipomotaosides and their recognition by COX-1 and 2Estrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT000990958.pdf.txt000990958.pdf.txtExtracted Texttext/plain30278http://www.lume.ufrgs.br/bitstream/10183/267616/2/000990958.pdf.txt80baacb2a5733840c05edce6d6edeef0MD52ORIGINAL000990958.pdfTexto completo (inglês)application/pdf1378579http://www.lume.ufrgs.br/bitstream/10183/267616/1/000990958.pdf0a58304292af887b79c33db5e58a25edMD5110183/2676162023-12-06 04:24:40.956798oai:www.lume.ufrgs.br:10183/267616Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-12-06T06:24:40Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
title |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
spellingShingle |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 Arantes, Pablo Ricardo Ipomotaosides Dinâmica molecular Dissacarídeos Ipomotaosides Resin glycosides Disaccharides Molecular dynamics Docking Inflammatory process |
title_short |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
title_full |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
title_fullStr |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
title_full_unstemmed |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
title_sort |
Conformational characterization of ipomotaosides and their recognition by COX-1 and 2 |
author |
Arantes, Pablo Ricardo |
author_facet |
Arantes, Pablo Ricardo Sachett, Liana Guimarães Graebin, Cedric Stephan Verli, Hugo |
author_role |
author |
author2 |
Sachett, Liana Guimarães Graebin, Cedric Stephan Verli, Hugo |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Arantes, Pablo Ricardo Sachett, Liana Guimarães Graebin, Cedric Stephan Verli, Hugo |
dc.subject.por.fl_str_mv |
Ipomotaosides Dinâmica molecular Dissacarídeos |
topic |
Ipomotaosides Dinâmica molecular Dissacarídeos Ipomotaosides Resin glycosides Disaccharides Molecular dynamics Docking Inflammatory process |
dc.subject.eng.fl_str_mv |
Ipomotaosides Resin glycosides Disaccharides Molecular dynamics Docking Inflammatory process |
description |
The aerial parts of Ipomoea batatas are described herein to produce four new resin glycosides, designated as ipomotaosides A, B, C, and D. Ipomotaoside A was found to present inhibitory activity on both cyclooxygenases. However, the conformational elucidation of these molecules may be difficult due to their high flexibility. In this context, the current work presents a conformational characterization of ipomotaosides A–D in aqueous and nonaqueous solvents. The employed protocol includes metadynamics evaluation and unrestrained molecular dynamics simulations (MD). The obtained data provided structural models for the ipomotaosides in good agreement with previous ROESY distances measured in pyridine. Accordingly, the most abundant conformation of ipomotaoside A in solution was employed in flexible docking studies, providing a structural basis for the compound’s inhibition of COX enzymes. The so-obtained complex supports resin glycosides’ role as original scaffolds for future studies, aiming at structural optimization and development of potential new anti-inflammatory agents. |
publishDate |
2014 |
dc.date.issued.fl_str_mv |
2014 |
dc.date.accessioned.fl_str_mv |
2023-11-25T03:26:15Z |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/267616 |
dc.identifier.issn.pt_BR.fl_str_mv |
1420-3049 |
dc.identifier.nrb.pt_BR.fl_str_mv |
000990958 |
identifier_str_mv |
1420-3049 000990958 |
url |
http://hdl.handle.net/10183/267616 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Molecules. Basel, SW. Vol. 19, no. 4 (2014), p. 5421-5433 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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