Abstract
A new method for obtaining 4-(2-methyl-1,3-oxazol-5-yl)benzenesulfonamide, an antiglaucomatous drug candidate oxazopt, was developed using a diazotization reaction. A combined potentiated effect of the antimicrobial action of carbapenems (meropenem) and aminoglycosides (gentamicin) against antibiotic-resistant gram-positive bacteria Enterococcus faecium, Enterococcus faecalis and gram-negative bacteria Escherichia coli, and antimonooxidase effect in vitro was revealed for this compound.
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Funding
The synthesis and study of the antimonoamine oxidase activity of the compounds was carried out with the financial support of the Russian Science Foundation (grant No. 22-13-20085). The antibacterial properties and potentiation effects of the drug candidate oxazopt were carried out at the expense of the Ministry of Education (state assignment 073-00077-21-02 “Development of an innovative drug against glaucoma based on selective inhibition of carbonic anhydrase II,” registration number 730000F.99.1.BV10AA00006).
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Gasilina, O.A., Romanycheva, A.A., Shetnev, A.A. et al. Synthesis, Antibacterial, and Antimonooxidase Activity of 4-(2-Methyl-1,3-oxazol-5-yl)benzenesulfonamide. Russ J Gen Chem 93, 2749–2755 (2023). https://doi.org/10.1134/S1070363223110038
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DOI: https://doi.org/10.1134/S1070363223110038