4.7 Article

TAK-599, a novel N-phosphono type prodrug of Anti-MRSA cephalosporin T-91825:: Synthesis, physicochemical and pharmacological properties

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 11, Issue 11, Pages 2427-2437

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0968-0896(03)00126-3

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Crystalline 1 (TAK-599) is a novel N-phosphono prodrug of anti-methicillin-resistant Staphylococcus aureus (MRSA) cephalosporin 2a (T-91825) that has high affinity for penicillin-binding protein (PBP) 2' (IC50; 0.90 mug/mL) and shows potent in vitro anti-MRSA activity (MIC against MRSA N133; 1.56 mug/mL), comparable to that of vancomycin (1.56 mug/mL). Although 2a had insufficient water solubility (2.3 mg/mL) for parenteral administration, 1 showed excellent water solubility (> 100 mg/mL, pH 7) as well as good chemical stability in the solid state and solution. In pharmacokinetic studies, when 1 was administered intravenously to rats and monkeys, it was rapidly converted into 2a in the blood. These results show that 1 (TAK-599) is a highly promising parenteral cephalosporin targeted for MRSA infection. (C) 2003 Elsevier Science Ltd. All rights reserved.

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