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Calculation of lipophilicity for Pt(II) complexes: Experimental comparison of several methods

Tetko, Igor V., Jaroszewicz, Iwona, Platts, James Alexis ORCID: https://orcid.org/0000-0002-1008-6595 and Kuduk-Jaworska, Janina 2008. Calculation of lipophilicity for Pt(II) complexes: Experimental comparison of several methods. Journal of Inorganic Biochemistry 102 (7) , pp. 1424-1437. 10.1016/j.jinorgbio.2007.12.029

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Abstract

Platinum containing compounds are promising antitumor agents, but must enter cells before reaching their main biological target, namely DNA. Their distribution within the body, and hence their activity is to a large extent determined by their lipophilicity, thus there is a strong interest to develop computational methods to predict this important property. This study analyses accuracy of five methods, namely ALOGPS, KOWWIN, CLOGP and two quantum chemical approaches, to predict octanol/water partition coefficients (log P) for sets of 43 and 12 Pt(II) complexes, collected from the literature and measured by the authors, respectively. All methods gave generally poor results with mean absolute error (MAE) of between 0.8 and 3 log units for prediction of new compounds. Extension of the ALOGPS program with data from the literature set resulted in the best prediction ability, MAE = 0.46, for the measured molecules. The program was also able to correctly predict errors in calculated log P values. It is freely available for interactive use at http://www.vcclab.org.

Item Type: Article
Status: Published
Schools: Chemistry
Uncontrolled Keywords: Log Po/w; Partition coefficient; Lipophilicity; Platinum complexes; QSPR
Publisher: Elsevier
ISSN: 0162-0134
Last Modified: 17 Oct 2022 09:55
URI: https://orca.cardiff.ac.uk/id/eprint/6147

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