Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities
ABSTRACT: Six derivatives of the known biopesticide rotenone were prepared by several chemical transformations. Rotenone and its derivatives showed differential in vitro antiparasitic activity and selective cytotoxicity. In general, compounds were more active against Plasmodium falciparum than Leish...
- Autores:
-
Upegui Zapata, Yulieth Alexandra
Gil Romero, Juan Fernando
Quiñones Fletcher, Winston
Torres, Fernando
Escobar Peláez, Gustavo
Robledo Restrepo, Sara María
Echeverri López, Luis Fernando
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2014
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/23682
- Acceso en línea:
- http://hdl.handle.net/10495/23682
- Palabra clave:
- Antiparasitarios
Antiparasitic Agents
Rotenona
Rotenone
Citotoxicidad
Cytotoxicity
Transformaciones químicas
http://aims.fao.org/aos/agrovoc/c_6665
http://aims.fao.org/aos/agrovoc/c_34251
https://id.nlm.nih.gov/mesh/D000977
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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| dc.title.spa.fl_str_mv |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| title |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| spellingShingle |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities Antiparasitarios Antiparasitic Agents Rotenona Rotenone Citotoxicidad Cytotoxicity Transformaciones químicas http://aims.fao.org/aos/agrovoc/c_6665 http://aims.fao.org/aos/agrovoc/c_34251 https://id.nlm.nih.gov/mesh/D000977 |
| title_short |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| title_full |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| title_fullStr |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| title_full_unstemmed |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| title_sort |
Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities |
| dc.creator.fl_str_mv |
Upegui Zapata, Yulieth Alexandra Gil Romero, Juan Fernando Quiñones Fletcher, Winston Torres, Fernando Escobar Peláez, Gustavo Robledo Restrepo, Sara María Echeverri López, Luis Fernando |
| dc.contributor.author.none.fl_str_mv |
Upegui Zapata, Yulieth Alexandra Gil Romero, Juan Fernando Quiñones Fletcher, Winston Torres, Fernando Escobar Peláez, Gustavo Robledo Restrepo, Sara María Echeverri López, Luis Fernando |
| dc.contributor.researchgroup.spa.fl_str_mv |
Programa de Estudio y Control de Enfermedades Tropicales (PECET) Química Orgánica de Productos Naturales |
| dc.subject.decs.none.fl_str_mv |
Antiparasitarios Antiparasitic Agents |
| topic |
Antiparasitarios Antiparasitic Agents Rotenona Rotenone Citotoxicidad Cytotoxicity Transformaciones químicas http://aims.fao.org/aos/agrovoc/c_6665 http://aims.fao.org/aos/agrovoc/c_34251 https://id.nlm.nih.gov/mesh/D000977 |
| dc.subject.agrovoc.none.fl_str_mv |
Rotenona Rotenone Citotoxicidad Cytotoxicity |
| dc.subject.proposal.spa.fl_str_mv |
Transformaciones químicas |
| dc.subject.agrovocuri.none.fl_str_mv |
http://aims.fao.org/aos/agrovoc/c_6665 http://aims.fao.org/aos/agrovoc/c_34251 |
| dc.subject.meshuri.none.fl_str_mv |
https://id.nlm.nih.gov/mesh/D000977 |
| description |
ABSTRACT: Six derivatives of the known biopesticide rotenone were prepared by several chemical transformations. Rotenone and its derivatives showed differential in vitro antiparasitic activity and selective cytotoxicity. In general, compounds were more active against Plasmodium falciparum than Leishmania panamensis. Rotenone had an EC50 of 19.0 µM against P. falciparum, and 127.2 µM against L. panamensis. Although chemical transformation does not improve its biological profile against P. falciparum, three of its derivatives showed a significant level of action within an adequate range of activity with EC50 values < 50.0 µM. This antiplasmodial activity was not due to red blood cell hemolysis, since LC50 was >>400 µM. On the other hand, all derivatives displayed a non-specific cytotoxicity on several cell lines and primary human cell cultures. |
| publishDate |
2014 |
| dc.date.issued.none.fl_str_mv |
2014 |
| dc.date.accessioned.none.fl_str_mv |
2021-11-02T13:24:53Z |
| dc.date.available.none.fl_str_mv |
2021-11-02T13:24:53Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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publishedVersion |
| dc.identifier.citation.spa.fl_str_mv |
Upegui, Y., Gil, J., Quiñones, W., Torres, F., Escobar, G., Robledo, S., & Echeverri, F. (2014). Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities. Molecules, 19(11), 18911–18922. Retrieved from http://dx.doi.org/10.3390/molecules191118911 |
| dc.identifier.issn.none.fl_str_mv |
1420-3049 |
| dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10495/23682 |
| dc.identifier.doi.none.fl_str_mv |
10.3390/molecules191118911 |
| identifier_str_mv |
Upegui, Y., Gil, J., Quiñones, W., Torres, F., Escobar, G., Robledo, S., & Echeverri, F. (2014). Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities. Molecules, 19(11), 18911–18922. Retrieved from http://dx.doi.org/10.3390/molecules191118911 1420-3049 10.3390/molecules191118911 |
| url |
http://hdl.handle.net/10495/23682 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Molecules |
| dc.relation.citationendpage.spa.fl_str_mv |
18922 |
| dc.relation.citationissue.spa.fl_str_mv |
11 |
| dc.relation.citationstartpage.spa.fl_str_mv |
18911 |
| dc.relation.citationvolume.spa.fl_str_mv |
19 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Molecules |
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http://creativecommons.org/licenses/by/2.5/co/ |
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https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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openAccess |
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12 |
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application/pdf |
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MDPI |
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Basilea, Suiza |
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Upegui Zapata, Yulieth AlexandraGil Romero, Juan FernandoQuiñones Fletcher, WinstonTorres, FernandoEscobar Peláez, GustavoRobledo Restrepo, Sara MaríaEcheverri López, Luis FernandoPrograma de Estudio y Control de Enfermedades Tropicales (PECET)Química Orgánica de Productos Naturales2021-11-02T13:24:53Z2021-11-02T13:24:53Z2014Upegui, Y., Gil, J., Quiñones, W., Torres, F., Escobar, G., Robledo, S., & Echeverri, F. (2014). Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities. Molecules, 19(11), 18911–18922. Retrieved from http://dx.doi.org/10.3390/molecules1911189111420-3049http://hdl.handle.net/10495/2368210.3390/molecules191118911ABSTRACT: Six derivatives of the known biopesticide rotenone were prepared by several chemical transformations. Rotenone and its derivatives showed differential in vitro antiparasitic activity and selective cytotoxicity. In general, compounds were more active against Plasmodium falciparum than Leishmania panamensis. Rotenone had an EC50 of 19.0 µM against P. falciparum, and 127.2 µM against L. panamensis. Although chemical transformation does not improve its biological profile against P. falciparum, three of its derivatives showed a significant level of action within an adequate range of activity with EC50 values < 50.0 µM. This antiplasmodial activity was not due to red blood cell hemolysis, since LC50 was >>400 µM. On the other hand, all derivatives displayed a non-specific cytotoxicity on several cell lines and primary human cell cultures.COL0015339COL001509912application/pdfengMDPIBasilea, Suizahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic ActivitiesArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAntiparasitariosAntiparasitic AgentsRotenonaRotenoneCitotoxicidadCytotoxicityTransformaciones químicashttp://aims.fao.org/aos/agrovoc/c_6665http://aims.fao.org/aos/agrovoc/c_34251https://id.nlm.nih.gov/mesh/D000977Molecules18922111891119MoleculesPublicationORIGINALUpeguiYulieth_2014_PreparationRotenoneAntimalarial.pdfUpeguiYulieth_2014_PreparationRotenoneAntimalarial.pdfArtículo de investigaciónapplication/pdf267077https://bibliotecadigital.udea.edu.co/bitstreams/2c33f8f3-290c-4b22-9b59-886ad66746d7/download8a9e84170f2df2cfa67a2bf2d4facf5bMD51trueAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/081c6838-aa7d-4492-b36e-5ba49b461cdf/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/ff679211-6a52-4a5d-ac7e-9b9bacc5bb88/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADTEXTUpeguiYulieth_2014_PreparationRotenoneAntimalarial.pdf.txtUpeguiYulieth_2014_PreparationRotenoneAntimalarial.pdf.txtExtracted texttext/plain78453https://bibliotecadigital.udea.edu.co/bitstreams/ef21d0c7-2fd8-45bc-b7cd-916f3602cd52/download6fae9f53cebda8495362dc11a342f94dMD54falseAnonymousREADTHUMBNAILUpeguiYulieth_2014_PreparationRotenoneAntimalarial.pdf.jpgUpeguiYulieth_2014_PreparationRotenoneAntimalarial.pdf.jpgGenerated Thumbnailimage/jpeg14300https://bibliotecadigital.udea.edu.co/bitstreams/1a43e538-4ac5-4403-a8c6-7de456819137/download9750999761d048821a0b8869653aceadMD55falseAnonymousREAD10495/23682oai:bibliotecadigital.udea.edu.co:10495/236822025-03-26 19:47:33.35http://creativecommons.org/licenses/by/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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 |
