Transcriptional drug repositioning and cheminformatics approach for differentiation therapy of leukaemia cells.

Differentiation therapy is attracting increasing interest in cancer as it can be more specific than conventional chemotherapy approaches, and it has offered new treatment options for some cancer types, such as treating acute promyelocytic leukaemia (APL) by retinoic acid. However, there is a pressing need to identify additional molecules which act in this way, both in leukaemia and other cancer types. In this work, we hence developed a novel transcriptional drug repositioning approach, based on both bioinformatics and cheminformatics components, that enables selecting such compounds in a more informed manner. We have validated the approach for leukaemia cells, and retrospectively retinoic acid was successfully identified using our method. Prospectively, the anti-parasitic compound fenbendazole was tested in leukaemia cells, and we were able to show that it can induce the differentiation of leukaemia cells to granulocytes in low concentrations of 0.1 µM and within as short a time period as 3 days. This work hence provides a systematic and validated approach for identifying small molecules for differentiation therapy in cancer.

Hybrid Harris hawks optimization with cuckoo search for drug design and discovery in chemoinformatics.

One of the major drawbacks of cheminformatics is a large amount of information present in the datasets. In the majority of cases, this information contains redundant instances that affect the analysis of similarity measurements with respect to drug design and discovery. Therefore, using classical methods such as the protein bank database and quantum mechanical calculations are insufficient owing to the dimensionality of search spaces. In this paper, we introduce a hybrid metaheuristic algorithm called CHHO-CS, which combines Harris hawks optimizer (HHO) with two operators: cuckoo search (CS) and chaotic maps. The role of CS is to control the main position vectors of the HHO algorithm to maintain the balance between exploitation and exploration phases, while the chaotic maps are used to update the control energy parameters to avoid falling into local optimum and premature convergence. Feature selection (FS) is a tool that permits to reduce the dimensionality of the dataset by removing redundant and non desired information, then FS is very helpful in cheminformatics. FS methods employ a classifier that permits to identify the best subset of features. The support vector machines (SVMs) are then used by the proposed CHHO-CS as an objective function for the classification process in FS. The CHHO-CS-SVM is tested in the selection of appropriate chemical descriptors and compound activities. Various datasets are used to validate the efficiency of the proposed CHHO-CS-SVM approach including ten from the UCI machine learning repository. Additionally, two chemical datasets (i.e., quantitative structure-activity relation biodegradation and monoamine oxidase) were utilized for selecting the most significant chemical descriptors and chemical compounds activities. The extensive experimental and statistical analyses exhibit that the suggested CHHO-CS method accomplished much-preferred trade-off solutions over the competitor algorithms including the HHO, CS, particle swarm optimization, moth-flame optimization, grey wolf optimizer, Salp swarm algorithm, and sine-cosine algorithm surfaced in the literature. The experimental results proved that the complexity associated with cheminformatics can be handled using chaotic maps and hybridizing the meta-heuristic methods.

The Literature of Chemoinformatics: 1978-2018.

This article presents a study of the literature of chemoinformatics, updating and building upon an analogous bibliometric investigation that was published in 2008. Data on outputs in the field, and citations to those outputs, were obtained by means of topic searches of the Web of Science Core Collection. The searches demonstrate that chemoinformatics is by now a well-defined sub-discipline of chemistry, and one that forms an essential part of the chemical educational curriculum. There are three core journals for the subject: The Journal of Chemical Information and Modeling, the Journal of Cheminformatics, and Molecular Informatics, and, having established itself, chemoinformatics is now starting to export knowledge to disciplines outside of chemistry.

Comprehensive Analysis of Applicability Domains of QSPR Models for Chemical Reactions.

Nowadays, the problem of the model's applicability domain (AD) definition is an active research topic in chemoinformatics. Although many various AD definitions for the models predicting properties of molecules (Quantitative Structure-Activity/Property Relationship (QSAR/QSPR) models) were described in the literature, no one for chemical reactions (Quantitative Reaction-Property Relationships (QRPR)) has been reported to date. The point is that a chemical reaction is a much more complex object than an individual molecule, and its yield, thermodynamic and kinetic characteristics depend not only on the structures of reactants and products but also on experimental conditions. The QRPR models' performance largely depends on the way that chemical transformation is encoded. In this study, various AD definition methods extensively used in QSAR/QSPR studies of individual molecules, as well as several novel approaches suggested in this work for reactions, were benchmarked on several reaction datasets. The ability to exclude wrong reaction types, increase coverage, improve the model performance and detect Y-outliers were tested. As a result, several "best" AD definitions for the QRPR models predicting reaction characteristics have been revealed and tested on a previously published external dataset with a clear AD definition problem.

BRADSHAW: a system for automated molecular design.

This paper introduces BRADSHAW (Biological Response Analysis and Design System using an Heterogenous, Automated Workflow), a system for automated molecular design which integrates methods for chemical structure generation, experimental design, active learning and cheminformatics tools. The simple user interface is designed to facilitate access to large scale automated design whilst minimising software development required to introduce new algorithms, a critical requirement in what is a very fast moving field. The system embodies a philosophy of automation, best practice, experimental design and the use of both traditional cheminformatics and modern machine learning algorithms.