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dc.contributor.author
Boiani, Mariana
dc.contributor.author
Cerecetto, Hugo
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González, Mercedes
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Risso, Mariela
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Olea Azar, Claudio
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Piro, Oscar Enrique
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Castellano, Eduardo E.
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López De Ceráin, Adela
dc.contributor.author
Ezpeleta, Olga
dc.contributor.author
Monge Vega, Antonio
dc.date.available
2020-03-11T18:01:52Z
dc.date.issued
2001-12
dc.identifier.citation
Boiani, Mariana; Cerecetto, Hugo; González, Mercedes; Risso, Mariela; Olea Azar, Claudio; et al.; 1,2,5-Oxadiazole N-oxide derivatives as potential anti-cancer agents: Synthesis and biological evaluation. Part IV; Elsevier France-editions Scientifiques Medicales Elsevier; European Journal of Medical Chemistry; 36; 10; 12-2001; 771-782
dc.identifier.issn
0223-5234
dc.identifier.uri
http://hdl.handle.net/11336/99157
dc.description.abstract
Several new 1,2,5-oxadiazole N-oxide derivatives and some deoxygenated analogues were synthesized to be tested as potential selective hypoxic cell cytotoxins. Compounds prepared were designed in order to gain insight into the mechanism of action of this kind of cytotoxin. Compounds were tested in oxia and hypoxia and they proved to be non-selective. 3-Cyano-N2-oxide-4-phenyl-1,2,5-oxadiazole showed the best cytotoxic activity in oxia. The cytotoxicity observed for these derivatives could be explained in terms of the electronic characteristics of the 1,2,5-oxadiazole substituents. Electrochemical and ESR studies were performed on the more cytotoxic derivative. © 2001 Éditions scientifiques et médicales Elsevier SAS.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier France-editions Scientifiques Medicales Elsevier
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
1,2,5-OXADIAZOLE N-OXIDE
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ANTI-CANCER AGENTS
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STRUCTURE-ACTIVITY RELATIONSHIPS
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Física de los Materiales Condensados
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Ciencias Físicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
1,2,5-Oxadiazole N-oxide derivatives as potential anti-cancer agents: Synthesis and biological evaluation. Part IV
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-02-10T14:08:00Z
dc.journal.volume
36
dc.journal.number
10
dc.journal.pagination
771-782
dc.journal.pais
Francia
dc.description.fil
Fil: Boiani, Mariana. Universidad de la República Facultad de Química; Uruguay
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Fil: Cerecetto, Hugo. Universidad de la República Facultad de Química; Uruguay
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Fil: González, Mercedes. Universidad de la República Facultad de Química; Uruguay
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Fil: Risso, Mariela. Universidad de la República Facultad de Química; Uruguay
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Fil: Olea Azar, Claudio. Universidad de Chile; Chile
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Fil: Piro, Oscar Enrique. Facultad de Ciencias Exactas, Universidad Nacional de la Plata; Argentina
dc.description.fil
Fil: Castellano, Eduardo E.. Universidade de Sao Paulo; Brasil
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Fil: López De Ceráin, Adela. Universidad de Navarra; España
dc.description.fil
Fil: Ezpeleta, Olga. Universidad de Navarra; España
dc.description.fil
Fil: Monge Vega, Antonio. Universidad de Navarra; España
dc.journal.title
European Journal of Medical Chemistry
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/S0223-5234(01)01265-X
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S022352340101265X
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