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RUDN University pharmacists modeled derivative molecules of the antibacterial levofloxacin to find out what biological functions its individual structural fragments – pharmacophores – are responsible for. This is necessary to increase the effectiveness of the drug, as bacteria become increasingly resistant to antibiotics. The results were published in Scientia Pharmaceutica.
The antibacterial drug levofloxacin is used to treat pneumonia, sinusitis, genitourinary infections, and other diseases. It is included in the WHO Model List of Essential Medicines. In terms of its chemical structure, it is a third-generation fluoroquinolone – a completely synthetic substance of the quinolone type. Generation refers to different modifications of quinolones that are used in different areas. Quinolones of different generations are widely used, but bacteria – for example, pneumococcus and Staphylococcus aureus – develop resistance to them. RUDN University pharmacists studied several derivatives of levofloxacin to find potential candidates for new antibacterial drugs and find out which structural elements are responsible for the biological activity of the substances.
“One of the approaches to improve the kinetic and dynamic characteristics of drugs is to study the properties of the products that are formed as a result of their transformation,” Elena Uspenskaya, Doctor of Pharmaceutical Sciences, Professor, Associate Professor of the Department of Pharmaceutical and Toxicological Chemistry of the RUDN University said.
For the experiment, scientists used the pharmaceutical substance levofloxacin. To predict what biological activity its derivatives will have, the authors simulated them, as well as molecular docking “poses” on a computer (in silico). A total of five derivatives and levofloxacin itself were studied. Biological activity was assessed using 7 different types of activity: antibacterial and antitumor effects, inhibition of specific enzymes, and so on.
Modeling made it possible to determine which structural elements of levofloxacin are responsible for its action. Thus, without a carboxyl group in the composition, the antimicrobial activity of the substance is reduced by half. Non-standard actions appear – for example, suppression of the cytochrome P450 enzyme. For some of the most promising modifications, the authors obtained 3D renderings. Based on these results, it will be possible to search for new drugs based on levofloxacin.
“The in silico results allowed us to discover quantitative structure-activity correlations and predict the molecular mechanisms of activity. This is of applied interest for targeted drug search,” Elena Uspenskaya, Doctor of Pharmaceutical Sciences, Professor, Associate Professor of the Department of Pharmaceutical and Toxicological Chemistry of the RUDN University said.
