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...
- 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/
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|
| 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 |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
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 |
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 |
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https://creativecommons.org/licenses/by-nc-sa/4.0/ |
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http://creativecommons.org/licenses/by-nc-sa/2.5/co/ |
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Atribución-NoComercial-CompartirIgual 2.5 Colombia (CC BY-NC-SA 2.5 CO) |
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info:eu-repo/semantics/openAccess |
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http://purl.org/coar/access_right/c_abf2 |
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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 |
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openAccess |
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application/pdf |
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Universidad de Granada, Facultad de Farmacia |
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Granada, España |
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Universidad de Antioquia |
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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; 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