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...

Full description

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/
id UDEA2_5758e953e75226bbdaf5b11d139214e5
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/23682
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
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
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.version.spa.fl_str_mv info:eu-repo/semantics/publishedVersion
format http://purl.org/coar/resource_type/c_2df8fbb1
status_str 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
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by/2.5/co/
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by/4.0/
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.coar.spa.fl_str_mv http://purl.org/coar/access_right/c_abf2
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/co/
https://creativecommons.org/licenses/by/4.0/
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.extent.spa.fl_str_mv 12
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv MDPI
dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
bitstream.url.fl_str_mv https://bibliotecadigital.udea.edu.co/bitstreams/2c33f8f3-290c-4b22-9b59-886ad66746d7/download
https://bibliotecadigital.udea.edu.co/bitstreams/081c6838-aa7d-4492-b36e-5ba49b461cdf/download
https://bibliotecadigital.udea.edu.co/bitstreams/ff679211-6a52-4a5d-ac7e-9b9bacc5bb88/download
https://bibliotecadigital.udea.edu.co/bitstreams/ef21d0c7-2fd8-45bc-b7cd-916f3602cd52/download
https://bibliotecadigital.udea.edu.co/bitstreams/1a43e538-4ac5-4403-a8c6-7de456819137/download
bitstream.checksum.fl_str_mv 8a9e84170f2df2cfa67a2bf2d4facf5b
1646d1f6b96dbbbc38035efc9239ac9c
8a4605be74aa9ea9d79846c1fba20a33
6fae9f53cebda8495362dc11a342f94d
9750999761d048821a0b8869653acead
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv Repositorio Institucional de la Universidad de Antioquia
repository.mail.fl_str_mv aplicacionbibliotecadigitalbiblioteca@udea.edu.co
_version_ 1851052279322378240
spelling 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.coTk9URTogUExBQ0UgWU9VUiBPV04gTElDRU5TRSBIRVJFClRoaXMgc2FtcGxlIGxpY2Vuc2UgaXMgcHJvdmlkZWQgZm9yIGluZm9ybWF0aW9uYWwgcHVycG9zZXMgb25seS4KCk5PTi1FWENMVVNJVkUgRElTVFJJQlVUSU9OIExJQ0VOU0UKCkJ5IHNpZ25pbmcgYW5kIHN1Ym1pdHRpbmcgdGhpcyBsaWNlbnNlLCB5b3UgKHRoZSBhdXRob3Iocykgb3IgY29weXJpZ2h0Cm93bmVyKSBncmFudHMgdG8gRFNwYWNlIFVuaXZlcnNpdHkgKERTVSkgdGhlIG5vbi1leGNsdXNpdmUgcmlnaHQgdG8gcmVwcm9kdWNlLAp0cmFuc2xhdGUgKGFzIGRlZmluZWQgYmVsb3cpLCBhbmQvb3IgZGlzdHJpYnV0ZSB5b3VyIHN1Ym1pc3Npb24gKGluY2x1ZGluZwp0aGUgYWJzdHJhY3QpIHdvcmxkd2lkZSBpbiBwcmludCBhbmQgZWxlY3Ryb25pYyBmb3JtYXQgYW5kIGluIGFueSBtZWRpdW0sCmluY2x1ZGluZyBidXQgbm90IGxpbWl0ZWQgdG8gYXVkaW8gb3IgdmlkZW8uCgpZb3UgYWdyZWUgdGhhdCBEU1UgbWF5LCB3aXRob3V0IGNoYW5naW5nIHRoZSBjb250ZW50LCB0cmFuc2xhdGUgdGhlCnN1Ym1pc3Npb24gdG8gYW55IG1lZGl1bSBvciBmb3JtYXQgZm9yIHRoZSBwdXJwb3NlIG9mIHByZXNlcnZhdGlvbi4KCllvdSBhbHNvIGFncmVlIHRoYXQgRFNVIG1heSBrZWVwIG1vcmUgdGhhbiBvbmUgY29weSBvZiB0aGlzIHN1Ym1pc3Npb24gZm9yCnB1cnBvc2VzIG9mIHNlY3VyaXR5LCBiYWNrLXVwIGFuZCBwcmVzZXJ2YXRpb24uCgpZb3UgcmVwcmVzZW50IHRoYXQgdGhlIHN1Ym1pc3Npb24gaXMgeW91ciBvcmlnaW5hbCB3b3JrLCBhbmQgdGhhdCB5b3UgaGF2ZQp0aGUgcmlnaHQgdG8gZ3JhbnQgdGhlIHJpZ2h0cyBjb250YWluZWQgaW4gdGhpcyBsaWNlbnNlLiBZb3UgYWxzbyByZXByZXNlbnQKdGhhdCB5b3VyIHN1Ym1pc3Npb24gZG9lcyBub3QsIHRvIHRoZSBiZXN0IG9mIHlvdXIga25vd2xlZGdlLCBpbmZyaW5nZSB1cG9uCmFueW9uZSdzIGNvcHlyaWdodC4KCklmIHRoZSBzdWJtaXNzaW9uIGNvbnRhaW5zIG1hdGVyaWFsIGZvciB3aGljaCB5b3UgZG8gbm90IGhvbGQgY29weXJpZ2h0LAp5b3UgcmVwcmVzZW50IHRoYXQgeW91IGhhdmUgb2J0YWluZWQgdGhlIHVucmVzdHJpY3RlZCBwZXJtaXNzaW9uIG9mIHRoZQpjb3B5cmlnaHQgb3duZXIgdG8gZ3JhbnQgRFNVIHRoZSByaWdodHMgcmVxdWlyZWQgYnkgdGhpcyBsaWNlbnNlLCBhbmQgdGhhdApzdWNoIHRoaXJkLXBhcnR5IG93bmVkIG1hdGVyaWFsIGlzIGNsZWFybHkgaWRlbnRpZmllZCBhbmQgYWNrbm93bGVkZ2VkCndpdGhpbiB0aGUgdGV4dCBvciBjb250ZW50IG9mIHRoZSBzdWJtaXNzaW9uLgoKSUYgVEhFIFNVQk1JU1NJT04gSVMgQkFTRUQgVVBPTiBXT1JLIFRIQVQgSEFTIEJFRU4gU1BPTlNPUkVEIE9SIFNVUFBPUlRFRApCWSBBTiBBR0VOQ1kgT1IgT1JHQU5JWkFUSU9OIE9USEVSIFRIQU4gRFNVLCBZT1UgUkVQUkVTRU5UIFRIQVQgWU9VIEhBVkUKRlVMRklMTEVEIEFOWSBSSUdIVCBPRiBSRVZJRVcgT1IgT1RIRVIgT0JMSUdBVElPTlMgUkVRVUlSRUQgQlkgU1VDSApDT05UUkFDVCBPUiBBR1JFRU1FTlQuCgpEU1Ugd2lsbCBjbGVhcmx5IGlkZW50aWZ5IHlvdXIgbmFtZShzKSBhcyB0aGUgYXV0aG9yKHMpIG9yIG93bmVyKHMpIG9mIHRoZQpzdWJtaXNzaW9uLCBhbmQgd2lsbCBub3QgbWFrZSBhbnkgYWx0ZXJhdGlvbiwgb3RoZXIgdGhhbiBhcyBhbGxvd2VkIGJ5IHRoaXMKbGljZW5zZSwgdG8geW91ciBzdWJtaXNzaW9uLgo=