发明名称 PROCESS FOR PREPARING CEPHALOSPORIN DERIVATIVES
摘要 <p>Cephalosporins of formula (I) and their acid-addn. salts and solvates are new. In formula (I), R1 is H or a protecting gp; R2 and R3 are each Me or Et; R4 is Me, Et, n-Pr, n-Bu, allyl, 2-butenyl, 3-butenyl, CH2CH2OH, CH2CH2CH2OH, CH2NMe2, pyridylmethyl, pyridylethyl, benzyl or phenethyl. (I) are antibacterial agents active against Gram- positive and -negative bacteria, e.g. with MIC values of 0.18-0.50 mcg/ml against cephalothinresistant E. coli and K. pneumoniae and 3.2-7.9 mcg/ml against Ps. aeruginosa.</p>
申请公布号 KR900005047(B1) 申请公布日期 1990.07.18
申请号 KR19830001218 申请日期 1983.03.25
申请人 BRISTOL-MYERS RES INST 发明人 HAJIME KAMACHI;JUN OKUMURA;TAKAYUKI NAITO
分类号 C07D501/06;A61K;A61K31/34;A61K31/45;A61K31/545;A61K31/546;A61P31/04;C07D;C07D501/00;C07D501/02;C07D501/16;C07D501/20;C07D501/24;C07D501/38;C07D501/46;(IPC1-7):C07D501/46 主分类号 C07D501/06
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