Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/212581 |
Resumo: | Trichomonas vaginalis and Leishmania spp. are protozoal species responsible for millions of cases of parasitic diseases worldwide. Considering the potential of natural products and the need for more effective and less toxic alternatives to treat trichomoniasis and leishmaniasis, this study aimed to evaluate the effect of two series of triterpenes derivatives with different modifications at C-3 and C-28 positions of the ursolic acid (UA) and betulinic acid (BA) against trophozoites of Trichomonas vaginalis and promastigotes forms of Leishmania (L.) amazonensis. The compounds modified just at C-3 were the most active. The 3β-acetyl betulinic acid (1b) reduced the trophozoites viability of T. vaginalis at 74%, followed by the 3-oxo ursolic acid and 3-oxo betulinic acid (3a and 3b) compounds (55% of reduction). The compound 3β-isobutyl ursolic acid (7a) inhibited the viability of L. amazonensis promastigotes by 55%. Therefore, analyzing the structure-activity relationship and the data of literature, it is possible to suppose that the inclusion of polar groups in the skeletons could improve the antiprotozoal activity. Overall, further studies are necessary to develop triterpenic derivatives with more powerful trichomonicidal and leishmanicidal properties. |
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Cargnin, Simone TascaStaudt, Andressa FinklerMenezes, Camila BrazSantos, Ana Paula de Azevedo dosFialho, Saara NeriTasca, TianaTeles, Carolina Bioni GarciaGnoatto, Simone Cristina Baggio2020-08-04T03:38:40Z20191984-8250http://hdl.handle.net/10183/212581001116212Trichomonas vaginalis and Leishmania spp. are protozoal species responsible for millions of cases of parasitic diseases worldwide. Considering the potential of natural products and the need for more effective and less toxic alternatives to treat trichomoniasis and leishmaniasis, this study aimed to evaluate the effect of two series of triterpenes derivatives with different modifications at C-3 and C-28 positions of the ursolic acid (UA) and betulinic acid (BA) against trophozoites of Trichomonas vaginalis and promastigotes forms of Leishmania (L.) amazonensis. The compounds modified just at C-3 were the most active. The 3β-acetyl betulinic acid (1b) reduced the trophozoites viability of T. vaginalis at 74%, followed by the 3-oxo ursolic acid and 3-oxo betulinic acid (3a and 3b) compounds (55% of reduction). The compound 3β-isobutyl ursolic acid (7a) inhibited the viability of L. amazonensis promastigotes by 55%. Therefore, analyzing the structure-activity relationship and the data of literature, it is possible to suppose that the inclusion of polar groups in the skeletons could improve the antiprotozoal activity. Overall, further studies are necessary to develop triterpenic derivatives with more powerful trichomonicidal and leishmanicidal properties.application/pdfengBrazilian journal of pharmaceutical sciences. Vol. 55 (2019), e17481, [7 p.]FarmáciaTrichomonas vaginalisBetulinic acideLeishmania amazonensisSemisynthesisUrsolic acidEvaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalisinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001116212.pdf.txt001116212.pdf.txtExtracted Texttext/plain25492http://www.lume.ufrgs.br/bitstream/10183/212581/2/001116212.pdf.txt5adf1d533adce628fbeea45c45d6e880MD52ORIGINAL001116212.pdfTexto completo (inglês)application/pdf834447http://www.lume.ufrgs.br/bitstream/10183/212581/1/001116212.pdf05743e4aeb18ac142ec3944de392a4acMD5110183/2125812020-08-05 03:39:06.937316oai:www.lume.ufrgs.br:10183/212581Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2020-08-05T06:39:06Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
title |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
spellingShingle |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis Cargnin, Simone Tasca Farmácia Trichomonas vaginalis Betulinic acide Leishmania amazonensis Semisynthesis Ursolic acid |
title_short |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
title_full |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
title_fullStr |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
title_full_unstemmed |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
title_sort |
Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis |
author |
Cargnin, Simone Tasca |
author_facet |
Cargnin, Simone Tasca Staudt, Andressa Finkler Menezes, Camila Braz Santos, Ana Paula de Azevedo dos Fialho, Saara Neri Tasca, Tiana Teles, Carolina Bioni Garcia Gnoatto, Simone Cristina Baggio |
author_role |
author |
author2 |
Staudt, Andressa Finkler Menezes, Camila Braz Santos, Ana Paula de Azevedo dos Fialho, Saara Neri Tasca, Tiana Teles, Carolina Bioni Garcia Gnoatto, Simone Cristina Baggio |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Cargnin, Simone Tasca Staudt, Andressa Finkler Menezes, Camila Braz Santos, Ana Paula de Azevedo dos Fialho, Saara Neri Tasca, Tiana Teles, Carolina Bioni Garcia Gnoatto, Simone Cristina Baggio |
dc.subject.por.fl_str_mv |
Farmácia Trichomonas vaginalis |
topic |
Farmácia Trichomonas vaginalis Betulinic acide Leishmania amazonensis Semisynthesis Ursolic acid |
dc.subject.eng.fl_str_mv |
Betulinic acide Leishmania amazonensis Semisynthesis Ursolic acid |
description |
Trichomonas vaginalis and Leishmania spp. are protozoal species responsible for millions of cases of parasitic diseases worldwide. Considering the potential of natural products and the need for more effective and less toxic alternatives to treat trichomoniasis and leishmaniasis, this study aimed to evaluate the effect of two series of triterpenes derivatives with different modifications at C-3 and C-28 positions of the ursolic acid (UA) and betulinic acid (BA) against trophozoites of Trichomonas vaginalis and promastigotes forms of Leishmania (L.) amazonensis. The compounds modified just at C-3 were the most active. The 3β-acetyl betulinic acid (1b) reduced the trophozoites viability of T. vaginalis at 74%, followed by the 3-oxo ursolic acid and 3-oxo betulinic acid (3a and 3b) compounds (55% of reduction). The compound 3β-isobutyl ursolic acid (7a) inhibited the viability of L. amazonensis promastigotes by 55%. Therefore, analyzing the structure-activity relationship and the data of literature, it is possible to suppose that the inclusion of polar groups in the skeletons could improve the antiprotozoal activity. Overall, further studies are necessary to develop triterpenic derivatives with more powerful trichomonicidal and leishmanicidal properties. |
publishDate |
2019 |
dc.date.issued.fl_str_mv |
2019 |
dc.date.accessioned.fl_str_mv |
2020-08-04T03:38:40Z |
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info:eu-repo/semantics/article info:eu-repo/semantics/other |
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info:eu-repo/semantics/publishedVersion |
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publishedVersion |
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http://hdl.handle.net/10183/212581 |
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1984-8250 |
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001116212 |
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http://hdl.handle.net/10183/212581 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Brazilian journal of pharmaceutical sciences. Vol. 55 (2019), e17481, [7 p.] |
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info:eu-repo/semantics/openAccess |
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openAccess |
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