An FtsZ-targeting prodrug with oral antistaphylococcal efficacy in vivo.

Abstract

The bacterial cell division protein FtsZ represents a novel antibiotic target that has yet to be exploited clinically. The benzamide PC190723 was among the first FtsZ-targeting compounds to exhibit in vivo efficacy in a murine infection model system. Despite its initial promise, the poor formulation properties of the compound have limited its potential for clinical development. We describe here the development of an N-Mannich base derivative of PC190723 with enhanced drug-like properties and oral in vivo efficacy. The N-Mannich base derivative (TXY436) is ∼100-fold more soluble than PC190723 in an acidic aqueous vehicle (10 mM citrate, pH 2.6) suitable for oral in vivo administration. At physiological pH (7.4), TXY436 acts as a prodrug, converting to PC190723 with a conversion half-life of 18.2 ± 1.6 min. Pharmacokinetic analysis following intravenous administration of TXY436 into mice yielded elimination half-lives of 0.26 and 0.96 h for the TXY436 prodrug and its PC190723 product, respectively. In addition, TXY436 was found to be orally bioavailable and associated with significant extravascular distribution. Using a mouse model of systemic infection with methicillin-sensitive Staphylococcus aureus or methicillin-resistant S. aureus, we show that TXY436 is efficacious in vivo upon oral administration. In contrast, the oral administration of PC190723 was not efficacious. Mammalian cytotoxicity studies of TXY436 using Vero cells revealed an absence of toxicity up to compound concentrations at least 64 times greater than those associated with antistaphylococcal activity. These collective properties make TXY436 a worthy candidate for further investigation as a clinically useful agent for the treatment of staphylococcal infections.

• Authors: Malvika Kaul, Lilly Mark, Yongzheng Zhang, Ajit K Parhi, Edmond J Lavoie, Daniel S Pilch
• Journal: Antimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 57 Issue 12 Pg. 5860-9 (Dec 2013) ISSN: 1098-6596 [Electronic] United States
• PMID: 24041882 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Bacterial Agents
• Bacterial Proteins
• Benzamides
• Cytoskeletal Proteins
• FtsZ protein, Bacteria
• PC190723
• Prodrugs
• Pyridines
• TXY436
• Thiazoles

Topics

• Animals
• Anti-Bacterial Agents (metabolism, pharmacokinetics, pharmacology)
• Bacterial Proteins (antagonists & inhibitors, metabolism)
• Benzamides (metabolism, pharmacokinetics, pharmacology)
• Biological Availability
• Biotransformation
• Chlorocebus aethiops
• Cytoskeletal Proteins (antagonists & inhibitors, metabolism)
• Female
• Half-Life
• Male
• Methicillin-Resistant Staphylococcus aureus (drug effects, growth & development)
• Mice
• Mice, Inbred BALB C
• Microbial Sensitivity Tests
• Prodrugs (metabolism, pharmacokinetics, pharmacology)
• Pyridines (metabolism, pharmacokinetics, pharmacology)
• Staphylococcal Infections (drug therapy, microbiology)
• Thiazoles (metabolism, pharmacokinetics, pharmacology)
• Vero Cells