Antibiotic resistance and drug modification: Synthesis, characterization and bioactivity of newly modified potent pleuromutilin derivatives with a substituted piperazine moiety

• Published in: Bioorganic chemistry Vol. 132; pp. 106353 - 106369
• Main Authors: Yi, Yunpeng, Yang, Shifa, Liu, Yueyue, Yin, Bin, Zhao, Zengcheng, Li, Guiming, Huang, Zhongli, Chen, Lei, Liu, Fei, Shang, Ruofeng, Lin, Shuqian
• Format: Journal Article
• Language: English
• Published: SAN DIEGO Elsevier Inc 01.03.2023; Elsevier
• Subjects: Animals; Anti-Bacterial Agents - chemistry; Antibacterial activity; Biochemistry & Molecular Biology; Chemistry; Chemistry, Organic; Drug Resistance, Microbial; Life Sciences & Biomedicine; Methicillin-Resistant Staphylococcus aureus; Mice; Microbial Sensitivity Tests; Molecular docking; Molecular Docking Simulation; Physical Sciences; Piperazine - pharmacology; Pleuromutilin derivatives; Pleuromutilins; Science & Technology; Staphylococcal Infections - drug therapy; Staphylococcus aureus; Staphylococcus epidermidis; Synthesis; Antibacterial activity; Pleuromutilin derivatives; Synthesis; Molecular docking; STRAINS; BINDING
• ISSN: 0045-2068; 1090-2120
• DOI: 10.1016/j.bioorg.2023.106353

[Display omitted] •A series of novel pleuromutilin derivatives with substituted piperazine moieties were synthesized.•Synthesized compounds were evaluated for their antibacterial activity.•Compound 6l showed excellent antibacterial activity.•Compound 6l displayed rapid bactericidal activity and potent therapeutic efficacy in mouse systemic infection. Antibiotic-resistant bacteria pose a major global public health concern, owing to the lack of effective antibacterial drugs. Consequently, the discovery and development of innovative antibacterial drug classes with unique mechanisms of action are urgently needed. In this study, we designed, synthesised, and tested a series of novel pleuromutilin derivatives with piperazine linker substituted by amino acids moieties to determine their antibacterial properties. Most synthesized compounds exhibited potent activities against Staphylococcus aureus (S. aureus), methicillin-resistant S. aureus (MRSA), and methicillin-resistant Staphylococcus epidermidis. Compound 6l, the most potent antibacterial agent created in this study, displayed a rapid bactericidal activity against MRSA, Klebsiella pneumoniae and S. aureus cfr N12. Moreover, pharmacokinetics study of compound 6l exhibited good PK performance with a low in vivo clearance (CL = 1965 mL/h/kg) and a suitable half-life (T1/2 = 11.614 ± 5.123 h). Molecular docking experiments revealed the binding model of compound 6l to the unmethylated A2503 of peptidyl transferase centre of 23S rRNA. Interaction pattern of 6l with cfr-mediated ribosomes revealed by molecular dynamics. Moreover in vivo mouse systemic infection experiments with compound 6l revealed its effectiveness against MRSA and S. aureus cfr N12 with the ED50 of 11.08 mg/kg and 14.63 mg/kg body weight, respectively.