Design, synthesis, and evaluation of novel pleuromutilin aryl acrylate derivatives as promising broad-spectrum antibiotics especially for combatting multi-drug resistant gram-negative bacteria
- Eur J Med Chem. 2023 Nov 5;259:115653. doi: 10.1016/j.ejmech.2023.115653.
- 1. College of Pharmacy, Xinjiang Medical University, No.567 Shangde North Road, Urumqi, Xinjiang, 830001, PR China. Electronic address: [email protected].
- 2. School of Biological and Pharmaceutical Sciences, Shaanxi University of Science & Technology, Xi'an, 710021, PR China.
- 3. College of Pharmacy, Xinjiang Medical University, No.567 Shangde North Road, Urumqi, Xinjiang, 830001, PR China.
- 4. Shaanxi Panlong Pharmaceutical Group Co., Ltd., Xi'an, 710025, PR China.
- 5. School of Biological and Pharmaceutical Sciences, Shaanxi University of Science & Technology, Xi'an, 710021, PR China. Electronic address: [email protected].
- 6. Shaanxi Pioneer Biotech Co., Ltd., Xi'an, 710021, PR China.
- 7. School of Biological and Pharmaceutical Sciences, Shaanxi University of Science & Technology, Xi'an, 710021, PR China. Electronic address: [email protected].
The emergence of drug-resistant strains presents a grave challenge for traditional Antibiotics, underscoring the exigency of exploring novel Antibacterial drugs. To address this, the present study endeavors to design and synthesize a collection of pleuromutilin aromatic acrylate derivatives, guided by combination principles. The Antibacterial activity and structure-activity relationship of these derivatives were evaluated, and most of the derivatives displayed moderate to excellent Antibacterial activity against both Gram-positive bacteria and Gram-negative bacteria. Among these derivatives, 5g exhibited the strongest Antibacterial activity, with MIC (minimum inhibitory concentration) values ranging from 1-32 μg/mL, and a MIC value against clinically isolated drug-resistant strains of 4-64 μg/mL. Additionally, 5g exhibited negligible cytotoxicity, superior anti-mycoplasma activity, and a greater propensity to perturb Bacterial cell membranes. Notably, the administration of 5g resulted in an increased survival rate of MRSA (Methicillin-resistant Staphylococcus aureus)-infected mice, with an ED50 (median effective dose) value of 9.04 mg/kg. These results indicated the potential of 5g to be further developed as an Antibacterial drug for the clinical treatment of drug-resistant Bacterial infections.
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