Improvement Biological Activity of Tetracycline Drug
摘要
The development of innovative antibiotic medications is particularly crucial since the increased bacterial resistance to antibiotics poses a serious danger to human health. Here, an adamantine moiety-containing family of Schiff base tetracycline derivatives was created and the structural characterization of the compounds was carried out via spectral methods (FTIR and 1H NMR), after which the physical properties of the synthesis compounds and the biological activity were tested in vitro. The Schiff bases derived from tetracycline show significantly higher activity against Gram-positive bacteria as compared to tetracycline. Further study on these derived compounds will help in marketing new derivatives of tetracycline that will have more broad-spectrum activity than tetracycline.