dc.creatorRodríguez, María Rosa
dc.creatorDuchowicz, Pablo Román
dc.creatorComelli, Nieves Carolina
dc.date.accessioned2022-08-09T14:12:19Z
dc.date.accessioned2022-10-15T14:47:32Z
dc.date.available2022-08-09T14:12:19Z
dc.date.available2022-10-15T14:47:32Z
dc.date.created2022-08-09T14:12:19Z
dc.date.issued2021-01
dc.identifierRodríguez, María Rosa; Duchowicz, Pablo Román; Comelli, Nieves Carolina; QSAR Classification of Anticancer Heterocyclichydrazones with Reactivity Descriptors; IGI GLOBAL; International Journal of Quantitative Structure-Property Relationships; 6; 1; 1-2021; 45-62
dc.identifier2379-7487
dc.identifierhttp://hdl.handle.net/11336/164755
dc.identifier2379-7479
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4398595
dc.description.abstractIn this study, validated PLS-DA models that discriminate heterocyclichydrazones with potentanticancer activity (GI50/IC50<50x10-6M) from those with low activity (GI50/IC50>=50x10-6M) against the cancer cell lines HCT-116 (colon), OVCAR-8 (human ovary), HL-60 (leukemia),and SF-295 (glioblastoma) were developed. A dataset of 24-a-(N)-heterocyclichydrazones and 14N-acylhydrazonyl-thienyl and various global and local reactivity descriptors were used for modeling.The best models classified for training and test sets with an accuracy range between 67-100%, aclass specificity and sensitivity range between 71-100%, error rate range between 0-0.27, and nonerrorrate range between 0.73-1.0. An external set of 20 compounds was predicted and the modelsshowed which new compounds are not suggested for further biological investigation. The molecularproperties with impact on the modeled endpoints show that the antitumor activity can be improvedwith electron-acceptor N-acylhydrazonyl-thienyl derivatives and a-(N)-heterocyclichydrazones withmoderate electron-donating character.
dc.languageeng
dc.publisherIGI GLOBAL
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.igi-global.com/gateway/article/272073
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.4018/IJQSPR.2021010104
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCancer
dc.subjectEnzyme Ribonucleotide Reductase
dc.subjectGlobal and Local Reactivity Descriptors
dc.subjectHCT-116
dc.subjectHL-60
dc.subjectOVCAR-8
dc.subjectQuantitative StructureActivity Relationships
dc.subjectSF-295
dc.titleQSAR Classification of Anticancer Heterocyclichydrazones with Reactivity Descriptors
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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