发明名称 CEPHALOSPORIN PYRIDINIM COMPLEX
摘要 <p>PROBLEM TO BE SOLVED: To obtain the subject derivative, which is an antibiotic substance, comprising a specific cephalosporin pyridinium derivative, having a strong and a wide range of antimicrobial activities and especially effective against methicillin-resistant Staphylococcus aureus(MRSA), enterococci, pneumococci, etc. SOLUTION: This compound is a new cephalosporin pyridinium derivative represented by formula I [R<1> is H, a lower alkyl, a cycloalkyl or acetyl; X is CH or N; (n) is 0, 1 or 2; (m) is 0 or 1; R<2> is H, a lower alkyl, anω- hydroxyalkyl, benzyl, a lower alkyl-(substituted)heterocyclic group or a group represented by the formula CH2 CONR<4> R<5> (R<4> and R<5> are each H, anω- hydroxyalkyl, phenyl, benzyl, naphthyl, heterocylic group, etc.)] and is useful as an antimicrobial agent, etc., effective against methicillin-resistant Staphylococcus aureus(MRSA), enterococci, pneumococci, etc. The compound is obtained by reacting a compound represented by formula II with a heterocyclic carboxylic acid compound represented by formula III (R<f> is H or an amino-protecting group).</p>
申请公布号 JPH10120687(A) 申请公布日期 1998.05.12
申请号 JP19970285233 申请日期 1997.10.17
申请人 F HOFFMANN LA ROCHE AG 发明人 ANGEHRN PETER;HEINZE-KRAUSS INGRID;PAGE MALCOLM;WEISS URS
分类号 C07D501/04;A61K31/545;A61K31/546;A61P31/04;C07D501/00;C07D501/16;C07D501/24;C07D501/56;(IPC1-7):C07D501/56 主分类号 C07D501/04
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