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dc.creatorIbacache, Juana Andrea
dc.creatorValderrama, Jaime A.
dc.creatorArancibia, Verónica
dc.creatorTheoduloz, Cristina
dc.creatorMuccioli, Giulio G.
dc.creatorBenites, Julio
dc.date2017-05-29
dc.date.accessioned2019-11-13T15:11:24Z
dc.date.available2019-11-13T15:11:24Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/108
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/112541
dc.descriptionA variety of 6-bromine-containing 7-anilino-1-arylisoquinolinequinones 2a-g were synthesized to evaluate their half-wave potentials and in vitro antiproliferative activity on gastric and leukemia cancer cell lines. The new compounds displayed significant IC50 values in the range: 1.31 to 11.04 μM. The structure activity relationship analysis of the new series suggest that the antiproliferative activity is dependent, in part, on the push-pull electronic effects of the nitrogen and bromine substituents inserted into the redox fragment of the 1-arylisoquinolinequinone scaffold. Linear regression analysis provided satisfactory relationships between the log IC50 and ClogP values for the AGS gastric cancer cell line. en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/108/94
dc.rightsCopyright (c) 2017 Juana Andrea Ibacache, Jaime A. Valderrama, Verónica Arancibia, Cristina Theoduloz, Giulio G. Muccioli, Julio Benitesen-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 61 No 4 (2016): Journal of the Chilean Chemical Societyen-US
dc.source0717-9707
dc.source0717-9324
dc.subjectIsoquinolinequinonesen-US
dc.subjectHalf-wave potentialsen-US
dc.subjectMTT assayen-US
dc.subjectAntiproliferative activityen-US
dc.titleANTIPROLIFERATIVE ACTIVITY OF NEW 6-BROMINE DERIVATIVES OF 7-ANILINO-1- ARYLISOQUINOLINEQUINONESen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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