News Release

Kazan University chemists teach neural networks to predict properties of compounds

A new joint Russian-French-Japanese paper appeared in Journal of Chemical Information and Modeling

Peer-Reviewed Publication

Kazan Federal University

The international team works on a computational model able to predict the properties of new molecules based on the analysis of fundamental chemical laws. The project was supported by the Russian Science Foundation (title "Using AI methods for the planning of chemical synthesis").

Co-author, Associate Professor Timur Madzhidov, explains, "We offered a way to insert the preexisting chemical equations into some frameworks of machine learning. It was tested on the predictions of tautomeric constants and acidity, which are linked by the Kabachnik equation. Using the functional interdependency between them, the neural network learns how to predict both these properties."

Prototropic tautomerism is the phenomenon of reversible isomerism, in which isomers (substances having the same qualitative and quantitative composition, but differing in structure and properties) easily transition into each other due to the transfer of a hydrogen atom.

"Tautomeric transformations are very common for organic compounds, being known for about half of all discovered compounds. For example, one of the mechanisms of spontaneous mutations is tied to the tautomeric transformations of DNA nucleic base. That why tautomerism must be taken into account when registering new compounds, during the computer design of new medications and the search for molecules with preconditioned properties," adds Madzhidov.

The results of this research can help increase the precision of prediction of physicochemical properties of designed medication and materials, as well as correctly forecast the parameters of chemical reactions.

Kazan Federal University, Lomonosov Moscow State University, the University of Hokkaido, and the University of Strasbourg contributed to the publication.


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