Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells

ABSTRACT: Synthesize tri-acyl ester derivatives of uridine, and evaluate its cytotoxicity against breast cancer cells line. Methods: The tri-esterified uridine derivatives were obtained through Steglich esterification reaction by fatty and aromatic acids, and with acetic anhydride. An acetonide deri...

Full description

Autores:
Berrío Escobar, Jhon Fernando
Arango Carmona, Victor Hugo
Galeano Jaramillo, Elkin de Jesús
Márquez Fernández, Diana Margarita
Márquez Fernández, Maria Elena
Camargo Guerrero, Mauricio
Martínez Martínez, Alejandro
Tipo de recurso:
Article of investigation
Fecha de publicación:
2016
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/13078
Acceso en línea:
http://hdl.handle.net/10495/13078
http://dx.doi.org/10.4321/S2340-98942016000400005
Palabra clave:
Nucleósidos
Nucleosides
Neoplasias de la Mama
Breast Neoplasms
Actividad citotóxica
Cáncer de mama
Derivados de uridina
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-sa/4.0/
id UDEA2_849c00ae655d4aac9e015866cdc5ef28
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/13078
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
dc.title.translated.spa.fl_str_mv Síntesis y actividad citotóxica de derivados triesterificados de la uridina en células de cáncer de mama
title Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
spellingShingle Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
Nucleósidos
Nucleosides
Neoplasias de la Mama
Breast Neoplasms
Actividad citotóxica
Cáncer de mama
Derivados de uridina
title_short Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
title_full Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
title_fullStr Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
title_full_unstemmed Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
title_sort Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells
dc.creator.fl_str_mv Berrío Escobar, Jhon Fernando
Arango Carmona, Victor Hugo
Galeano Jaramillo, Elkin de Jesús
Márquez Fernández, Diana Margarita
Márquez Fernández, Maria Elena
Camargo Guerrero, Mauricio
Martínez Martínez, Alejandro
dc.contributor.author.none.fl_str_mv Berrío Escobar, Jhon Fernando
Arango Carmona, Victor Hugo
Galeano Jaramillo, Elkin de Jesús
Márquez Fernández, Diana Margarita
Márquez Fernández, Maria Elena
Camargo Guerrero, Mauricio
Martínez Martínez, Alejandro
dc.contributor.researchgroup.spa.fl_str_mv Productos Naturales Marinos
Genética, Regeneración y Cáncer
dc.subject.decs.none.fl_str_mv Nucleósidos
Nucleosides
Neoplasias de la Mama
Breast Neoplasms
topic Nucleósidos
Nucleosides
Neoplasias de la Mama
Breast Neoplasms
Actividad citotóxica
Cáncer de mama
Derivados de uridina
dc.subject.proposal.spa.fl_str_mv Actividad citotóxica
Cáncer de mama
Derivados de uridina
description ABSTRACT: Synthesize tri-acyl ester derivatives of uridine, and evaluate its cytotoxicity against breast cancer cells line. Methods: The tri-esterified uridine derivatives were obtained through Steglich esterification reaction by fatty and aromatic acids, and with acetic anhydride. An acetonide derivative from uridine was prepared with acid catalysis. Compounds were characterized by NMR spectroscopy (1H NMR and 13C NMR), and mass spectrometry. Derivatives were assessed in chinese hamster ovary (CHO-K1) and human breast cancer (MCF-7) cell lines. Results: Five tri-acyl ester derivatives of uridine were obtained one acetic acid, three fatty acids (myristic acid, stearic acid and oleic acid) with an aromatic acid. The uridine per-acetylated and uridine acetonide were obtained in high yields, however, the tri-acyl ester derivatives of uridine with fatty and aromatic acids were obtained in moderate and low yields, respectively. The acetonide and compounds 2 and 3 exhibited a cell viability inhibition significant on both cell lines to the higher concentration. Conclusions: Esterification method with coupling agents allowed obtained tri-acyl ester uridine derivatives with aliphatic and aromatic acids. However, significant cytotoxic activity (p<0.05) for uridine and its derivatives was not observed.
publishDate 2016
dc.date.issued.none.fl_str_mv 2016
dc.date.accessioned.none.fl_str_mv 2020-01-11T23:40:36Z
dc.date.available.none.fl_str_mv 2020-01-11T23:40:36Z
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 Berrío Escobar, J. F., Arango Carmona, V. H., Galeano Jaramillo, E., Márquez Fernández, D. M., Márquez Fernández, M. E., Camargo Guerrero, M., Martínez Martínez, A. (2016). Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells. Ars Pharmaceutica, 57(4), 183-191. http://dx.doi.org/10.4321/S2340-98942016000400005
dc.identifier.issn.none.fl_str_mv 0004-2927
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/13078
dc.identifier.doi.none.fl_str_mv http://dx.doi.org/10.4321/S2340-98942016000400005
dc.identifier.eissn.none.fl_str_mv 2340-9894
identifier_str_mv Berrío Escobar, J. F., Arango Carmona, V. H., Galeano Jaramillo, E., Márquez Fernández, D. M., Márquez Fernández, M. E., Camargo Guerrero, M., Martínez Martínez, A. (2016). Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells. Ars Pharmaceutica, 57(4), 183-191. http://dx.doi.org/10.4321/S2340-98942016000400005
0004-2927
2340-9894
url http://hdl.handle.net/10495/13078
http://dx.doi.org/10.4321/S2340-98942016000400005
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Ars Pharm.
dc.relation.citationendpage.spa.fl_str_mv 191
dc.relation.citationissue.spa.fl_str_mv 4
dc.relation.citationstartpage.spa.fl_str_mv 183
dc.relation.citationvolume.spa.fl_str_mv 57
dc.relation.ispartofjournal.spa.fl_str_mv Ars Pharmaceutica
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by-nc-sa/2.5/co/
dc.rights.accessrights.*.fl_str_mv Atribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO)
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 https://creativecommons.org/licenses/by-nc-sa/4.0/
http://creativecommons.org/licenses/by-nc-sa/2.5/co/
Atribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO)
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Universidad de Granada, Facultad de Farmacia
dc.publisher.place.spa.fl_str_mv Granada, España
institution Universidad de Antioquia
bitstream.url.fl_str_mv https://bibliotecadigital.udea.edu.co/bitstreams/5e2772dc-29ec-4cda-be93-3e2efb1c52f0/download
https://bibliotecadigital.udea.edu.co/bitstreams/6a18b56b-0827-4500-bac3-d913e1267373/download
https://bibliotecadigital.udea.edu.co/bitstreams/e6ba45ba-c6b8-4320-a130-c26f82ae763f/download
https://bibliotecadigital.udea.edu.co/bitstreams/c541a4f3-49dd-4db8-a6fa-562790c7a7c1/download
https://bibliotecadigital.udea.edu.co/bitstreams/2edcebce-9ce6-4472-9224-b7b16a804ab7/download
https://bibliotecadigital.udea.edu.co/bitstreams/c402187b-ae52-4a19-8610-6db4b7e108ae/download
https://bibliotecadigital.udea.edu.co/bitstreams/167f5aaa-b137-4ced-9e62-0ce80aac92dc/download
bitstream.checksum.fl_str_mv 03c25045d9266019224b60d6c5806bd8
4afdbb8c545fd630ea7db775da747b2f
d41d8cd98f00b204e9800998ecf8427e
d41d8cd98f00b204e9800998ecf8427e
8a4605be74aa9ea9d79846c1fba20a33
65665e176d7e333453698e4b096f110d
207e0041abbbcf73119c59d362918601
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
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_ 1851052597717237760
spelling Berrío Escobar, Jhon FernandoArango Carmona, Victor HugoGaleano Jaramillo, Elkin de JesúsMárquez Fernández, Diana MargaritaMárquez Fernández, Maria ElenaCamargo Guerrero, MauricioMartínez Martínez, AlejandroProductos Naturales MarinosGenética, Regeneración y Cáncer2020-01-11T23:40:36Z2020-01-11T23:40:36Z2016Berrío Escobar, J. F., Arango Carmona, V. H., Galeano Jaramillo, E., Márquez Fernández, D. M., Márquez Fernández, M. E., Camargo Guerrero, M., Martínez Martínez, A. (2016). Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cells. Ars Pharmaceutica, 57(4), 183-191. http://dx.doi.org/10.4321/S2340-989420160004000050004-2927http://hdl.handle.net/10495/13078http://dx.doi.org/10.4321/S2340-989420160004000052340-9894ABSTRACT: Synthesize tri-acyl ester derivatives of uridine, and evaluate its cytotoxicity against breast cancer cells line. Methods: The tri-esterified uridine derivatives were obtained through Steglich esterification reaction by fatty and aromatic acids, and with acetic anhydride. An acetonide derivative from uridine was prepared with acid catalysis. Compounds were characterized by NMR spectroscopy (1H NMR and 13C NMR), and mass spectrometry. Derivatives were assessed in chinese hamster ovary (CHO-K1) and human breast cancer (MCF-7) cell lines. Results: Five tri-acyl ester derivatives of uridine were obtained one acetic acid, three fatty acids (myristic acid, stearic acid and oleic acid) with an aromatic acid. The uridine per-acetylated and uridine acetonide were obtained in high yields, however, the tri-acyl ester derivatives of uridine with fatty and aromatic acids were obtained in moderate and low yields, respectively. The acetonide and compounds 2 and 3 exhibited a cell viability inhibition significant on both cell lines to the higher concentration. Conclusions: Esterification method with coupling agents allowed obtained tri-acyl ester uridine derivatives with aliphatic and aromatic acids. However, significant cytotoxic activity (p<0.05) for uridine and its derivatives was not observed.RESUMEN: Sintetizar derivados triesterificados de la uridina y evaluar su citotóxicidad sobre una línea celular de cáncer de mama. Métodos: Se prepararon derivados triesterificados de la uridina mediante la esterificación de Steglich para los ácidos grasos y aromáticos, y con anhídrido acético. Además se preparó el derivado acetonido mediante catálisis ácida. Los compuestos se caracterizaron por espectroscopia de RMN (RMN 1H y RMN 13C), y espectrometría de masas. Los derivados se evaluaron sobre líneas celulares de tumor de ovario de hámster chino (CHO) y de cáncer de mamá (MCF-7). Resultados: Se obtuvieron cinco derivados triesterificados de la uridina, uno con ácido acético, tres con ácidos grasos (ácido mirístico, ácido esteárico y ácido oleico) y uno con ácido aromático. Los derivados de uridina per-acetilada y acetonido se obtuvieron con rendimientos altos, sin embargo los derivados con ácidos grasos y aromático, se obtuvieron con rendimientos moderados y bajo, respectivamente. El acetonido y los compuestos 2 y 3, exhibieron inhibición significativa de la viabilidad celular sobre ambas líneas a la concentración más alta evaluada. Conclusiones: El método de esterificación con agentes de acoplamiento utilizado, permitió obtener derivados triesterificados de la uridina con ácidos grasos y aromáticos. No se observó actividad citotóxica significativa (p<0,05) para la uridina y sus derivados.COL0015043COL0006769application/pdfengUniversidad de Granada, Facultad de FarmaciaGranada, Españahttps://creativecommons.org/licenses/by-nc-sa/4.0/http://creativecommons.org/licenses/by-nc-sa/2.5/co/Atribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO)info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Synthesis and cytotoxic activity of tri-acyl ester derivatives of uridine in breast cancer cellsSíntesis y actividad citotóxica de derivados triesterificados de la uridina en células de cáncer de mamaArtículo 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/publishedVersionNucleósidosNucleosidesNeoplasias de la MamaBreast NeoplasmsActividad citotóxicaCáncer de mamaDerivados de uridinaArs Pharm.191418357Ars PharmaceuticaPublicationORIGINALMartinezAlejandro_2016_SynthesisCytotoxicActivity.pdfMartinezAlejandro_2016_SynthesisCytotoxicActivity.pdfArtículo de investigaciónapplication/pdf714304https://bibliotecadigital.udea.edu.co/bitstreams/5e2772dc-29ec-4cda-be93-3e2efb1c52f0/download03c25045d9266019224b60d6c5806bd8MD51trueAnonymousREADCC-LICENSElicense_urllicense_urltext/plain; charset=utf-849https://bibliotecadigital.udea.edu.co/bitstreams/6a18b56b-0827-4500-bac3-d913e1267373/download4afdbb8c545fd630ea7db775da747b2fMD52falseAnonymousREADlicense_textlicense_texttext/html; charset=utf-80https://bibliotecadigital.udea.edu.co/bitstreams/e6ba45ba-c6b8-4320-a130-c26f82ae763f/downloadd41d8cd98f00b204e9800998ecf8427eMD53falseAnonymousREADlicense_rdflicense_rdfapplication/rdf+xml; charset=utf-80https://bibliotecadigital.udea.edu.co/bitstreams/c541a4f3-49dd-4db8-a6fa-562790c7a7c1/downloadd41d8cd98f00b204e9800998ecf8427eMD54falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/2edcebce-9ce6-4472-9224-b7b16a804ab7/download8a4605be74aa9ea9d79846c1fba20a33MD55falseAnonymousREADTEXTMartinezAlejandro_2016_SynthesisCytotoxicActivity.pdf.txtMartinezAlejandro_2016_SynthesisCytotoxicActivity.pdf.txtExtracted texttext/plain32034https://bibliotecadigital.udea.edu.co/bitstreams/c402187b-ae52-4a19-8610-6db4b7e108ae/download65665e176d7e333453698e4b096f110dMD56falseAnonymousREADTHUMBNAILMartinezAlejandro_2016_SynthesisCytotoxicActivity.pdf.jpgMartinezAlejandro_2016_SynthesisCytotoxicActivity.pdf.jpgGenerated Thumbnailimage/jpeg12722https://bibliotecadigital.udea.edu.co/bitstreams/167f5aaa-b137-4ced-9e62-0ce80aac92dc/download207e0041abbbcf73119c59d362918601MD57falseAnonymousREAD10495/13078oai:bibliotecadigital.udea.edu.co:10495/130782025-03-27 00:50:17.031https://creativecommons.org/licenses/by-nc-sa/4.0/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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