BackgroundCheminformaticians are equipped with a very rich toolbox when carrying out molecular similarity calculations. A large number of molecular representations exist, and there are several methods (similarity and distance metrics) to quantify the similarity of molecular representations. In this work, eight well-known similarity/distance metrics are compared on a large dataset of molecular fingerprints with sum of ranking differences (SRD) and ANOVA analysis. The effects of molecular size, selection methods and data pretreatment methods on the outcome of the comparison are also assessed.ResultsA supplier database (https://mcule.com/) was used as the source of compounds for the similarity calculations in this study. A large number of datasets, each consisting of one hundred compounds, were compiled, molecular fingerprints were generated and similarity values between a randomly chosen reference compound and the rest were calculated for each dataset. Similarity metrics were compared based on their ranking of the compounds within one experiment (one dataset) using sum of ranking differences (SRD), while the results of the entire set of experiments were summarized on box and whisker plots. Finally, the effects of various factors (data pretreatment, molecule size, selection method) were evaluated with analysis of variance (ANOVA).ConclusionsThis study complements previous efforts to examine and rank various metrics for molecular similarity calculations. Here, however, an entirely general approach was taken to neglect any a priori knowledge on the compounds involved, as well as any bias introduced by examining only one or a few specific scenarios. The Tanimoto index, Dice index, Cosine coefficient and Soergel distance were identified to be the best (and in some sense equivalent) metrics for similarity calculations, i.e. these metrics could produce the rankings closest to the composite (average) ranking of the eight metrics. The similarity metrics derived from Euclidean and Manhattan distances are not recommended on their own, although their variability and diversity from other similarity metrics might be advantageous in certain cases (e.g. for data fusion). Conclusions are also drawn regarding the effects of molecule size, selection method and data pretreatment on the ranking behavior of the studied metrics.Graphical AbstractA visual summary of the comparison of similarity metrics with sum of ranking differences (SRD).Electronic supplementary materialThe online version of this article (doi:10.1186/s13321-015-0069-3) contains supplementary material, which is available to authorized users.

The kinetics of the redox reactions of the peroxomonosulfate ion (HSO(5)(-)) with iron(II), vanadium(IV), cerium(III), chloride, bromide, and iodide ions were studied. Cerium(III) is only oxidized upon illumination by UV light and cerium(IV) is produced in a photoreaction with a quantum yield of 0.33 +/- 0.03. Iron(II) and vanadium(IV) are most probably oxidized through one-electron transfer producing sulfate ion radicals as intermediates. The halide ions are oxidized in a formally two-electron process, which most likely includes oxygen-atom transfer. Comparison with literature data suggests that the activation entropies might be used as indicators distinguishing between heterolytic and homolytic cleavage of the peroxo bond in the redox reactions of HSO(5)(-).

The transcription factor STAT5 is an essential downstream mediator of many tyrosine kinases (TKs), particularly in hematopoietic cancers. STAT5 is activated by FLT3-ITD, which is a constitutively active TK driving the pathogenesis of acute myeloid leukemia (AML). Since STAT5 is a critical mediator of diverse malignant properties of AML cells, direct targeting of STAT5 is of significant clinical value. Here, we describe the development and preclinical evaluation of a novel, potent STAT5 SH2 domain inhibitor, AC-4–130, which can efficiently block pathological levels of STAT5 activity in AML. AC-4–130 directly binds to STAT5 and disrupts STAT5 activation, dimerization, nuclear translocation, and STAT5-dependent gene transcription. Notably, AC-4–130 substantially impaired the proliferation and clonogenic growth of human AML cell lines and primary FLT3-ITD+ AML patient cells in vitro and in vivo. Furthermore, AC-4–130 synergistically increased the cytotoxicity of the JAK1/2 inhibitor Ruxolitinib and the p300/pCAF inhibitor Garcinol. Overall, the synergistic effects of AC-4–130 with TK inhibitors (TKIs) as well as emerging treatment strategies provide new therapeutic opportunities for leukemia and potentially other cancers.

BackgroundInteraction fingerprints (IFP) have been repeatedly shown to be valuable tools in virtual screening to identify novel hit compounds that can subsequently be optimized to drug candidates. As a complementary method to ligand docking, IFPs can be applied to quantify the similarity of predicted binding poses to a reference binding pose. For this purpose, a large number of similarity metrics can be applied, and various parameters of the IFPs themselves can be customized. In a large-scale comparison, we have assessed the effect of similarity metrics and IFP configurations to a number of virtual screening scenarios with ten different protein targets and thousands of molecules. Particularly, the effect of considering general interaction definitions (such as Any Contact, Backbone Interaction and Sidechain Interaction), the effect of filtering methods and the different groups of similarity metrics were studied.ResultsThe performances were primarily compared based on AUC values, but we have also used the original similarity data for the comparison of similarity metrics with several statistical tests and the novel, robust sum of ranking differences (SRD) algorithm. With SRD, we can evaluate the consistency (or concordance) of the various similarity metrics to an ideal reference metric, which is provided by data fusion from the existing metrics. Different aspects of IFP configurations and similarity metrics were examined based on SRD values with analysis of variance (ANOVA) tests.ConclusionA general approach is provided that can be applied for the reliable interpretation and usage of similarity measures with interaction fingerprints. Metrics that are viable alternatives to the commonly used Tanimoto coefficient were identified based on a comparison with an ideal reference metric (consensus). A careful selection of the applied bits (interaction definitions) and IFP filtering rules can improve the results of virtual screening (in terms of their agreement with the consensus metric). The open-source Python package FPKit was introduced for the similarity calculations and IFP filtering; it is available at: https://github.com/davidbajusz/fpkit.Electronic supplementary materialThe online version of this article (10.1186/s13321-018-0302-y) contains supplementary material, which is available to authorized users.

Applied datasets can vary from a few hundred to thousands of samples in typical quantitative structure-activity/property (QSAR/QSPR) relationships and classification. However, the size of the datasets and the train/test split ratios can greatly affect the outcome of the models, and thus the classification performance itself. We compared several combinations of dataset sizes and split ratios with five different machine learning algorithms to find the differences or similarities and to select the best parameter settings in nonbinary (multiclass) classification. It is also known that the models are ranked differently according to the performance merit(s) used. Here, 25 performance parameters were calculated for each model, then factorial ANOVA was applied to compare the results. The results clearly show the differences not just between the applied machine learning algorithms but also between the dataset sizes and to a lesser extent the train/test split ratios. The XGBoost algorithm could outperform the others, even in multiclass modeling. The performance parameters reacted differently to the change of the sample set size; some of them were much more sensitive to this factor than the others. Moreover, significant differences could be detected between train/test split ratios as well, exerting a great effect on the test validation of our models.