| Autor: |
Shapovalova K; Gause Institute of New Antibiotics, 11 B. Pirogovskaya, 119021 Moscow, Russia., Zatonsky G; Gause Institute of New Antibiotics, 11 B. Pirogovskaya, 119021 Moscow, Russia., Grammatikova N; Gause Institute of New Antibiotics, 11 B. Pirogovskaya, 119021 Moscow, Russia., Osterman I; Center of Life Sciences, Skolkovo Institute of Science and Technology, Bolshoy Boulevard 30, bld. 1, 121205 Moscow, Russia.; Center for Translational Medicine, Sirius University of Science and Technology, Olympic Avenue 1, 354340 Sochi, Russia., Razumova E; Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1, 119991 Moscow, Russia., Shchekotikhin A; Gause Institute of New Antibiotics, 11 B. Pirogovskaya, 119021 Moscow, Russia., Tevyashova A; Gause Institute of New Antibiotics, 11 B. Pirogovskaya, 119021 Moscow, Russia. |
| Abstrakt: |
Aminoglycosides are one of the first classes of antibiotics to have been used clinically, and they are still being used today. They have a broad spectrum of antimicrobial activity, making them effective against many different types of bacteria. Despite their long history of use, aminoglycosides are still considered promising scaffolds for the development of new antibacterial agents, particularly as bacteria continue to develop resistances to existing antibiotics. We have synthesized a series of 6″-deoxykanamycin A analogues with additional protonatable groups (amino-, guanidino or pyridinium) and tested their biological activities. For the first time we have demonstrated the ability of the tetra- N -protected-6″- O -(2,4,6-triisopropylbenzenesulfonyl)kanamycin A to interact with a weak nucleophile, pyridine, resulting in the formation of the corresponding pyridinium derivative. Introducing small diamino-substituents at the 6″-position of kanamycin A did not significantly alter the antibacterial activity of the parent antibiotic, but further modification by acylation resulted in a complete loss of the antibacterial activity. However, introducing a guanidine residue led to a compound with improved activity against S. aureus . Moreover, most of the obtained 6″-modified kanamycin A derivatives were less influenced by the resistant mechanism associated with mutations of the elongation factor G than the parent kanamycin A. This suggests that modifying the 6″-position of kanamycin A with protonatable groups is a promising direction for the further development of new antibacterial agents with reduced resistances. |
