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Pyrazole-based analogs as potential antibacterial agents against methicillin-resistance staphylococcus aureus (MRSA)
Rameshwari Verma1, Santosh Kumar Verma1, Kadalipura P Rakesh2
1School of Chemistry and Chemical Engineering, Yulin University, Yulin, 719000, Shaanxi, PR China; Shaanxi Key Laboratory of Low Metamorphic Coal Clean Utilization, Yulin University, Yulin, 719000, Shaanxi, PR China.
Abstract:
Methicillin-resistant Staphylococcus aureus (MRSA) is becoming lethal to humanity due to easy transmission and difficult-to-treat skin and flimsy diseases. The most threatening aspect is the rapid resistance development of MRSA to any approved antibiotics, including vancomycin. The development of new, efficient, and nontoxic drug candidate to fight against MRSA isolates is the need of the hour. The intriguing molecular structure and versatile bioactive pyrazole core attracting to development required novel antibiotics. This review presents the decade developments of pyrazole-containing derivatives with a broad antibacterial movement against diverged bacterial strains. In specific, we correlated the efficacy of structurally diversified pyrazole analogs against MRSA and discussed different angles of structure-activity relationship (SAR). The current survey highlights pyrazole hybrids' present scenario on MRSA studies, covering articles published from 2011 to 2020. This collective information may become an excellent platform to plan and develop new pyrazole-based small MRSA growth inhibitors with minimal side effects.
Insights
New pyrazole derivatives show promise in combating Methicillin-resistant Staphylococcus aureus (MRSA), a dangerous superbug. This review explores pyrazole compounds developed between 2011-2020 for their effectiveness against MRSA, offering insights for future antibiotic development.
Area of Science:
- Medicinal Chemistry
- Microbiology
- Drug Discovery
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) poses a significant global health threat due to its increasing antibiotic resistance, including resistance to vancomycin.
- The urgent need for novel, effective, and safe antimicrobial agents against MRSA infections is paramount.
- Pyrazole scaffolds are recognized for their versatile bioactivity and potential in developing new therapeutic agents.
Purpose of the Study:
- To review and analyze the development of pyrazole-containing derivatives as potential antimicrobial agents against MRSA.
- To correlate the efficacy of structurally diverse pyrazole analogs with their structure-activity relationships (SAR) against MRSA.
- To provide a comprehensive overview of pyrazole hybrids in MRSA research from 2011 to 2020.
Main Methods:
- Systematic literature review of scientific articles published between 2011 and 2020.
- Analysis of structure-activity relationships (SAR) for pyrazole derivatives exhibiting antibacterial activity.
- Focus on studies specifically investigating the efficacy of pyrazole compounds against MRSA isolates.
Main Results:
- Numerous pyrazole derivatives have demonstrated broad-spectrum antibacterial activity, including against various bacterial strains.
- Specific pyrazole analogs and hybrids have shown significant efficacy against MRSA isolates.
- Structure-activity relationship studies have identified key molecular features contributing to the anti-MRSA activity of pyrazole compounds.
Conclusions:
- Pyrazole derivatives represent a promising class of compounds for the development of novel anti-MRSA agents.
- Further research into pyrazole hybrids can lead to the design of effective MRSA growth inhibitors with potentially reduced side effects.
- This review serves as a foundation for future drug discovery efforts targeting resistant bacterial infections.
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