The results obtained here show that the activity of these compounds is mainly determined by the JGI4-, PCR- , and Hy-values. The model provides important information on the structure–activity relationships of these types of compounds at the molecular level relevant for the design of new AA derivatives. The JGI4 of a potent agent should be

as low as possible while PCR- and Hy-values should be high. On the basis of these results in combination with previous evidences we can conclude that the interaction of the 1-[3-(4-arylpiperazin-1-yl)propyl]BAY 80-6946 molecular weight pyrrolidin-2-one moiety with the arrhythmic species is greatly increased by the structure and the geometry of the molecule rather than its physico-chemical properties. More extensive in silico studies are in progress and will be reported in due course. Acknowledgments GF120918 concentration This study was supported by the research grant from the UMK no. 29/2010. Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. Electronic Supplementary

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