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Medchemcomm. 2016 Sep 14;7(9):1819-1831. Epub 2016 Jul 22.

From linked open data to molecular interaction: studying selectivity trends for ligands of the human serotonin and dopamine transporter.

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1
Department of Pharmaceutical Chemistry , Pharmacoinformatics Research Group , University of Vienna , Althanstraße 14 , A-1090 , Austria . Email: barbara.zdrazil@univie.ac.at ; ; Tel: +43 1 4277 55110.

Abstract

Retrieval of congeneric and consistent SAR data sets for protein targets of interest is still a laborious task to do if no appropriate in-house data set is available. However, combining integrated open data sources (such as the Open PHACTS Discovery Platform) with workflow tools now offers the possibility of querying across multiple domains and tailoring the search to the given research question. Starting from two phylogenetically related protein targets of interest (the human serotonin and dopamine transporters), the whole chemical compound space was explored by implementing a scaffold-based clustering of compounds possessing biological measurements for both targets. In addition, potential hERG blocking liabilities were included. The workflow allowed studying the selectivity trends of scaffold series, identifying potentially harmful compound series, and performing SAR, docking studies and molecular dynamics (MD) simulations for a consistent data set of 56 cathinones. This delivered useful insights into driving determinants for hDAT selectivity over hSERT. With respect to the scaffold-based analyses it should be noted that the cathinone data set could be retrieved only when Murcko scaffold analyses were combined with similarity searches such as a common substructure search.

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