Comparative QSAR Analysis of 3,5-bis (Arylidene)-4-Piperidone Derivatives: the Development of Predictive Cytotoxicity Models

AuthorNajmeh Edrakien
AuthorUmashankar Dasen
AuthorBahram Hemateenejaden
AuthorJonathan R. Dimmocken
AuthorRamin Mirien
Issued Date2016-04-30en
Abstract1-[4-(2-Alkylaminoethoxy) phenylcarbonyl]-3,5-bis(arylidene)-4-piperidones are a novel class of potent cytotoxic agents. These compounds demonstrate low micromolar to submicromolar IC50 values against human Molt 4/C8 and CEM T-lymphocytes and murine leukemia L1210 cells. In this study, a comparative QSAR investigation was performed on a series of 3,5-bis (arylidene)-4-piperidones using different chemometric tools to develop the best predictive models for further development of analogs with improved cytotoxicity. All the QSAR models were validated by internal validation tests. The QSAR models obtained by GA-PLS method were considered the best as compared to MLR method. The best QSAR model obtained by GA-PLS analysis on L1210, CEM and Molt4/C8 demonstrated good predictively with R2pred values ranging from 0.94-0.80. Molecular density, topological (X2A) and geometrical indices of the molecules were found to be the most important factors for determining cytotoxic properties.en
DOIhttps://doi.org/10.22037/ijpr.2016.1845en
KeywordCytotoxicityen
Keyword3.5-bis(arylidene)-4-piperidonesen
KeywordQSARen
Keywordmultilinear regressionen
PublisherBrieflandsen
TitleComparative QSAR Analysis of 3,5-bis (Arylidene)-4-Piperidone Derivatives: the Development of Predictive Cytotoxicity Modelsen
TypeOriginal Articleen

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