Conformational characterization of ipomotaosides and their recognition by COX-1 and 2

Detalhes bibliográficos
Autor(a) principal: Arantes, Pablo Ricardo
Data de Publicação: 2014
Outros Autores: Sachett, Liana Guimarães, Graebin, Cedric Stephan, Verli, Hugo
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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spelling 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
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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
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000990958
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Molecules. Basel, SW. Vol. 19, no. 4 (2014), p. 5421-5433
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