(+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities

Detalhes bibliográficos
Autor(a) principal: Meleti, Vanderlisa Rita
Data de Publicação: 2020
Outros Autores: Esperandim, Viviane Rodrigues, Bocalon Flauzino, Luzio Gabriel, Prizantelli, Anna Helena, Lima Paula, Lucas Antonio de, Magalhaes, Lizandra Guidi, Cunha, Wilson Roberto, Laurentiz, Rosangela da Silva [UNESP], Rocha Pissurno, Ana Paula da [UNESP], Dhammika Nanayakkara, N. P., Pereira, Ana Carolina, Bastos, Jairo Kenupp, Tame Parreira, Renato Luis, Orenha, Renato Pereira, Andrade e Silva, Marcio Luis
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.actatropica.2019.105248
http://hdl.handle.net/11449/196772
Resumo: This paper reports the synthesis of (+/-)-licarin A 1, a dihydrobenzofuran neolignan, resultant of an oxidative coupling reaction of isoeugenol and horseradish peroxidase (HRP) enzyme. Following, three semi-synthetic derivatives from this compound were obtained: benzylated (+/-)-licarin A 2, methylated (+/-)-licarin A 3 and acetylated (+/-)-licarin A 4. After structural elucidation and assignment by Nuclear Magnetic Resonance of H-1, C-13 and DEPT, all compounds were evaluated in vitro against Trypomastigote forms of Trypanosoma cruzi (T. cruzi), the etiologic agent of Chagas disease, and Schistosoma mansoni (S. mansoni) worms, the etiologic agent of schistosomiasis. Compound (4) was the most active against S. mansoni adult worms, displaying worm viability reduction at 25 mu M and mortality of all worms at 100 and 200 mu M within 24 h. Compound 1 was the second most active, showing worm viability reduction at 50 mu M and mortality of 25% and 100% of worms in 24h at concentrations of 100 and 200 mu M, respectively. In addition, theoretical calculations aiming at finding molecular properties that showed the correlation for schistosomicidal and trypanocidal activities of (+/-)-licarin A and three of its semi-synthetic derivatives were also performed.
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spelling (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities(+/-)-Licarin ASemi-synthetic derivativesTrypanosoma cruziSchistosoma mansonicomputational studyThis paper reports the synthesis of (+/-)-licarin A 1, a dihydrobenzofuran neolignan, resultant of an oxidative coupling reaction of isoeugenol and horseradish peroxidase (HRP) enzyme. Following, three semi-synthetic derivatives from this compound were obtained: benzylated (+/-)-licarin A 2, methylated (+/-)-licarin A 3 and acetylated (+/-)-licarin A 4. After structural elucidation and assignment by Nuclear Magnetic Resonance of H-1, C-13 and DEPT, all compounds were evaluated in vitro against Trypomastigote forms of Trypanosoma cruzi (T. cruzi), the etiologic agent of Chagas disease, and Schistosoma mansoni (S. mansoni) worms, the etiologic agent of schistosomiasis. Compound (4) was the most active against S. mansoni adult worms, displaying worm viability reduction at 25 mu M and mortality of all worms at 100 and 200 mu M within 24 h. Compound 1 was the second most active, showing worm viability reduction at 50 mu M and mortality of 25% and 100% of worms in 24h at concentrations of 100 and 200 mu M, respectively. In addition, theoretical calculations aiming at finding molecular properties that showed the correlation for schistosomicidal and trypanocidal activities of (+/-)-licarin A and three of its semi-synthetic derivatives were also performed.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univ Franca, Nucleo Ciencias Exatas & Tecnol, Grp Pesquisa Produtos Nat, Ave Dr Armando Salles de Oliveira 201, BR-14404600 Franca, SP, BrazilUniv Sao Paulo, Escola Ciencias Farmaceut Ribeirao Preto, Ave Cafe S-N, BR-14040903 Ribeirao Preto, SP, BrazilUniv Mississippi, Sch Pharm, Dept Pharmacognosy, University, MS 38677 USAUniv Mississippi, Sch Pharm, Res Inst Pharmaceut Sci, Natl Ctr Nat Prod Res, University, MS 38677 USAUniv Estadual Paulista, Fac Engn, Dept Fis & Quim, Ilha Solteira, SP, BrazilIF Suldeminas, Ave Maria da Conceicao Santos,900 Parque Real, BR-37550000 Pouso Alegre, MG, BrazilUniv Estadual Paulista, Fac Engn, Dept Fis & Quim, Ilha Solteira, SP, BrazilFAPESP: 1998/14956-7FAPESP: 2009/05049-2FAPESP: 2011/07623-8FAPESP: 2017/24856-2Elsevier B.V.Univ FrancaUniversidade de São Paulo (USP)Univ MississippiUniversidade Estadual Paulista (Unesp)IF SuldeminasMeleti, Vanderlisa RitaEsperandim, Viviane RodriguesBocalon Flauzino, Luzio GabrielPrizantelli, Anna HelenaLima Paula, Lucas Antonio deMagalhaes, Lizandra GuidiCunha, Wilson RobertoLaurentiz, Rosangela da Silva [UNESP]Rocha Pissurno, Ana Paula da [UNESP]Dhammika Nanayakkara, N. P.Pereira, Ana CarolinaBastos, Jairo KenuppTame Parreira, Renato LuisOrenha, Renato PereiraAndrade e Silva, Marcio Luis2020-12-10T19:55:41Z2020-12-10T19:55:41Z2020-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article8http://dx.doi.org/10.1016/j.actatropica.2019.105248Acta Tropica. Amsterdam: Elsevier, v. 202, 8 p., 2020.0001-706Xhttp://hdl.handle.net/11449/19677210.1016/j.actatropica.2019.105248WOS:000525791600018Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Tropicainfo:eu-repo/semantics/openAccess2024-07-10T14:07:38Zoai:repositorio.unesp.br:11449/196772Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:23:36.712890Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
title (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
spellingShingle (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
Meleti, Vanderlisa Rita
(+/-)-Licarin A
Semi-synthetic derivatives
Trypanosoma cruzi
Schistosoma mansoni
computational study
title_short (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
title_full (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
title_fullStr (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
title_full_unstemmed (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
title_sort (+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
author Meleti, Vanderlisa Rita
author_facet Meleti, Vanderlisa Rita
Esperandim, Viviane Rodrigues
Bocalon Flauzino, Luzio Gabriel
Prizantelli, Anna Helena
Lima Paula, Lucas Antonio de
Magalhaes, Lizandra Guidi
Cunha, Wilson Roberto
Laurentiz, Rosangela da Silva [UNESP]
Rocha Pissurno, Ana Paula da [UNESP]
Dhammika Nanayakkara, N. P.
Pereira, Ana Carolina
Bastos, Jairo Kenupp
Tame Parreira, Renato Luis
Orenha, Renato Pereira
Andrade e Silva, Marcio Luis
author_role author
author2 Esperandim, Viviane Rodrigues
Bocalon Flauzino, Luzio Gabriel
Prizantelli, Anna Helena
Lima Paula, Lucas Antonio de
Magalhaes, Lizandra Guidi
Cunha, Wilson Roberto
Laurentiz, Rosangela da Silva [UNESP]
Rocha Pissurno, Ana Paula da [UNESP]
Dhammika Nanayakkara, N. P.
Pereira, Ana Carolina
Bastos, Jairo Kenupp
Tame Parreira, Renato Luis
Orenha, Renato Pereira
Andrade e Silva, Marcio Luis
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Franca
Universidade de São Paulo (USP)
Univ Mississippi
Universidade Estadual Paulista (Unesp)
IF Suldeminas
dc.contributor.author.fl_str_mv Meleti, Vanderlisa Rita
Esperandim, Viviane Rodrigues
Bocalon Flauzino, Luzio Gabriel
Prizantelli, Anna Helena
Lima Paula, Lucas Antonio de
Magalhaes, Lizandra Guidi
Cunha, Wilson Roberto
Laurentiz, Rosangela da Silva [UNESP]
Rocha Pissurno, Ana Paula da [UNESP]
Dhammika Nanayakkara, N. P.
Pereira, Ana Carolina
Bastos, Jairo Kenupp
Tame Parreira, Renato Luis
Orenha, Renato Pereira
Andrade e Silva, Marcio Luis
dc.subject.por.fl_str_mv (+/-)-Licarin A
Semi-synthetic derivatives
Trypanosoma cruzi
Schistosoma mansoni
computational study
topic (+/-)-Licarin A
Semi-synthetic derivatives
Trypanosoma cruzi
Schistosoma mansoni
computational study
description This paper reports the synthesis of (+/-)-licarin A 1, a dihydrobenzofuran neolignan, resultant of an oxidative coupling reaction of isoeugenol and horseradish peroxidase (HRP) enzyme. Following, three semi-synthetic derivatives from this compound were obtained: benzylated (+/-)-licarin A 2, methylated (+/-)-licarin A 3 and acetylated (+/-)-licarin A 4. After structural elucidation and assignment by Nuclear Magnetic Resonance of H-1, C-13 and DEPT, all compounds were evaluated in vitro against Trypomastigote forms of Trypanosoma cruzi (T. cruzi), the etiologic agent of Chagas disease, and Schistosoma mansoni (S. mansoni) worms, the etiologic agent of schistosomiasis. Compound (4) was the most active against S. mansoni adult worms, displaying worm viability reduction at 25 mu M and mortality of all worms at 100 and 200 mu M within 24 h. Compound 1 was the second most active, showing worm viability reduction at 50 mu M and mortality of 25% and 100% of worms in 24h at concentrations of 100 and 200 mu M, respectively. In addition, theoretical calculations aiming at finding molecular properties that showed the correlation for schistosomicidal and trypanocidal activities of (+/-)-licarin A and three of its semi-synthetic derivatives were also performed.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-10T19:55:41Z
2020-12-10T19:55:41Z
2020-02-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.actatropica.2019.105248
Acta Tropica. Amsterdam: Elsevier, v. 202, 8 p., 2020.
0001-706X
http://hdl.handle.net/11449/196772
10.1016/j.actatropica.2019.105248
WOS:000525791600018
url http://dx.doi.org/10.1016/j.actatropica.2019.105248
http://hdl.handle.net/11449/196772
identifier_str_mv Acta Tropica. Amsterdam: Elsevier, v. 202, 8 p., 2020.
0001-706X
10.1016/j.actatropica.2019.105248
WOS:000525791600018
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Acta Tropica
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 8
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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