CEPHALOSPORIN COMPOUNDS, THEIR PHARMACEUTICALLY ACCEPTABLE NONTOXIC SALTS, PHYSIOLOGICALLY HYDROLYZABLE ESTERS, ISOMERS HAVING E-CONFIGURATION OF DOUBLE BOND IN PROPENYL GROUP, SYN-ISOMERS AND OPTICAL ISOMERS AND A METHOD OF THEIR SYNTHESIS

The present invention relates to a cephalosporin compound represented by the following general formula (I) : its pharmaceutically acceptable non-toxic salt, physiologically hydrolyzable ester, hydrate or solvate, or isomers thereof, in which R represents hydrogen or an amino-protecting group, R and...

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Bibliographische Detailangaben
Hauptverfasser: CHAN SIK BANG, JONG TSU KIM, DEOG KHO YANG, KHUN SEUNG OKH, SE KHO KIM, DZHAE KHUN DZHEON, DZHAE KHONG JEO, JUNG MIN VU, SAM SIK KIM, DZHONG CHAN LIM, TAE KHI LI, MU JONG KIM
Format: Patent
Sprache:eng
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