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

被引:111
作者
Ishikawa, T [1 ]
Matsunaga, N [1 ]
Tawada, H [1 ]
Kuroda, N [1 ]
Nakayama, Y [1 ]
Ishibashi, Y [1 ]
Tomimoto, M [1 ]
Ikeda, Y [1 ]
Tagawa, Y [1 ]
Iizawa, Y [1 ]
Okonogi, K [1 ]
Hashiguchi, S [1 ]
Miyake, A [1 ]
机构
[1] Takeda Chem Ind Ltd, Div Pharmaceut Res, Yodogawa Ku, Osaka 5328686, Japan
关键词
D O I
10.1016/S0968-0896(03)00126-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2427 / 2437
页数:11
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