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Journal of Enzyme Inhibition and Medicinal Chemistry Volume 20, 2005 - Issue 1
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Research Article

Quantitative structure activity relationships (QSAR) of substituded (S)-phenylpiperidines as preferential dopamine autoreceptor antagonists

Eleni A. Pontiki Department of Pharmaceutical Chemistry, School of Pharmacy, Aristotelian University of Thessaloniki, 54124, Thessaloniki, Greece
,
Dimitra J. Hadjipavlou-Litina Department of Pharmaceutical Chemistry, School of Pharmacy, Aristotelian University of Thessaloniki, 54124, Thessaloniki, GreeceCorrespondence[email protected]
[email protected]
,
Athanassios M. Demertzis Department of Chemistry, University of Ioannina, 45110, Ioannina, Greece
,
Ioannis Hadjidakis Department of Chemistry, University of Ioannina, 45110, Ioannina, Greece
&
Dimitra Kovala-Demertzi Department of Chemistry, University of Ioannina, 45110, Ioannina, Greece
Pages 5-12 | Received 05 Dec 2003, Accepted 26 Jun 2004, Published online: 03 Oct 2008

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Mehdi Khoshneviszadeh & Amirhossein Sakhteman. (2016) Exploring quantitative structure–activity relationship (QSAR) models for some biologically active catechol structures using PC-LS-SVM and PC-ANFIS. Applied Biological Chemistry 59:3, pages 433-441.
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Fredrik Pettersson, Peder Svensson, Susanna Waters, Nicholas Waters & Clas Sonesson. (2013) Synthesis, pharmacological evaluation and QSAR modeling of mono-substituted 4-phenylpiperidines and 4-phenylpiperazines. European Journal of Medicinal Chemistry 62, pages 241-255.
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