| Literature DB >> 24378396 |
Karen L Lang1, Izabella T Silva2, Vanessa R Machado2, Lara A Zimmermann2, Miguel S B Caro3, Cláudia M O Simões2, Eloir P Schenkel2, Fernando J Durán4, Lílian S C Bernardes2, Eduardo B de Melo5.
Abstract
This article describes structure-activity relationship (SAR/QSAR) studies on the cytotoxic activity in a human lung adenocarcinoma cell line (A549) of 43 cucurbitacin derivatives. Modeling was performed using the methods partial least squares with discriminant analysis (PLS-DA) and PLS. For both studies, the variables were selected using the ordered predictor selection (OPS) algorithm. The SAR study demonstrated that the presence or absence of cytotoxic activity of the cucurbitacins could be described using information derived from their chemical structures. The QSAR study displayed suitable internal and external predictivity, and the selected descriptors indicated that the observed activity might be related to electrophilic attack on cellular structures or genetic material. This study provides improves the understanding of the cytotoxic activity of cucurbitacins and could be used to propose new cytotoxic agents.Entities:
Keywords: Cucurbitacins; Lung cancer; OPS; PLS; PLS-DA; QSAR
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Year: 2013 PMID: 24378396 DOI: 10.1016/j.jmgm.2013.12.004
Source DB: PubMed Journal: J Mol Graph Model ISSN: 1093-3263 Impact factor: 2.518