Analogues of Pyrimidine Nucleosides as Mycobacteria Growth Inhibitors.
Liudmila A AlexandrovaAnastasia L KhandazhinskayaElena S MatyuginaDmitriy A MakarovSergey N KochetkovPublished in: Microorganisms (2022)
Tuberculosis (TB) is the oldest human infection disease. Mortality from TB significantly decreased in the 20th century, because of vaccination and the widespread use of antibiotics. However, about a third of the world's population is currently infected with Mycobacterium tuberculosis ( Mtb ) and the death rate from TB is about 1.4-2 million people per year. In the second half of the 20th century, new extensively multidrug-resistant strains of Mtb were identified, which are steadily increasing among TB patients. Therefore, there is an urgent need to develop new anti-TB drugs, which remains one of the priorities of pharmacology and medicinal chemistry. The antimycobacterial activity of nucleoside derivatives and analogues was revealed not so long ago, and a lot of studies on their antibacterial properties have been published. Despite the fact that there are no clinically used drugs based on nucleoside analogues, some progress has been made in this area. This review summarizes current research in the field of the design and study of inhibitors of mycobacteria, primarily Mtb .
Keyphrases
- mycobacterium tuberculosis
- pulmonary tuberculosis
- multidrug resistant
- molecular docking
- end stage renal disease
- structure activity relationship
- endothelial cells
- ejection fraction
- newly diagnosed
- chronic kidney disease
- drug resistant
- escherichia coli
- acinetobacter baumannii
- emergency department
- prognostic factors
- type diabetes
- peritoneal dialysis
- cardiovascular disease
- randomized controlled trial
- risk factors
- gram negative
- klebsiella pneumoniae
- single cell
- coronary artery disease
- patient reported outcomes
- electronic health record
- cystic fibrosis
- adverse drug
- wound healing