Artículo
QSAR Classification of Anticancer Heterocyclichydrazones with Reactivity Descriptors
Fecha de publicación:
01/2021
Editorial:
IGI GLOBAL
Revista:
International Journal of Quantitative Structure-Property Relationships
ISSN:
2379-7487
e-ISSN:
2379-7479
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
In 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.
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Articulos(INIFTA)
Articulos de INST.DE INV.FISICOQUIMICAS TEORICAS Y APLIC.
Articulos de INST.DE INV.FISICOQUIMICAS TEORICAS Y APLIC.
Articulos(SEDE CENTRAL)
Articulos de SEDE CENTRAL
Articulos de SEDE CENTRAL
Citación
Rodríguez, 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
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