Article ID Journal Published Year Pages File Type
1371995 Bioorganic & Medicinal Chemistry Letters 2009 4 Pages PDF
Abstract

A phosphate prodrug strategy was investigated to address the problem of poor aqueous solubility of pleuromutilin analogues. Water-soluble phosphate prodrugs 6a, 6b and 6c of pleuromutilin analogues were designed and synthesized. Three compounds all exhibited excellent aqueous solubility (>50 mg/mL) at near-neutral pH and sufficient stability in buffer solution. In particular, the phenol pleuromutilin prodrug 6c displayed favourable pharmacokinetic profiles and comparable potency with vancomycin against MSSA and MRSA strains in vivo.

Graphical abstractSynthesis and biological properties of phosphate prodrugs of pleuromutilin analogues are disclosed. Compound 6c was metabolized efficiently to the biologically active parent 5d in vivo, it also showed excellent antibacterial activity against MSSA and MRSA with comparable ED50 as vancomycin by iv administration in mice.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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