(+/-)-Licarin A and its semi-synthetic derivatives: In vitro and in silico evaluation of trypanocidal and schistosomicidal activities
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , , , , |
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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(+/-)-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) |
repository.mail.fl_str_mv |
|
_version_ |
1808128804011376640 |