Kumar, AdarshSingh, Ankit KumarThareja, SureshKumar, Pradeep2024-01-212024-08-132024-01-212024-08-132022-07-062211352510.2174/2211352520666220705085733https://kr.cup.edu.in/handle/32116/3551Background: Methicillin-resistant Staphylococcus aureus (MRSA) is a Gram-positive strain whose resistance against existing antibiotics is a significant concern for researchers across the globe. Gram-positive infections, particularly methicillin-resistant Staphylococcus aureus spreading among S. aureus isolates, increased exponentially from 29% in 2009 to 47% in 2014. Literature reviews revealed that about 13-74% of S. aureus strains are Methicillin-resistant world-wide. Objective: In this article, we have summarized the mechanism of bacterium resistance, molecular targets to treat MRSA, and the activity of reported pyridine and pyrimidine derivatives against methicillin-resistant Staphylococcus aureus. Results: The data collected for this study from online peer-reviewed research articles and the Molecular-docking study of reported anti-MRSA agents performed using the Maestro Module of Schrodinger software. In silico studies showed that some pyridine derivatives have better binding interactions than standard anti-MRSA agents. Conclusion: Molecular docking studies of reported pyridine derivatives resulted in excellent hits for developing novel anti-MRSA agents. Overall, this study will be of immense importance for researchers designing and developing target-based anti-MRSA agents. � 2023 Bentham Science Publishers.en-USmolecular dockingMRSApyridinepyrimidineresistanceStaphylococcus aureusReviewhttps://www.eurekaselect.com/206610/article