摘要:
A compound of formula I or a physiologically acceptable salt thereof
wherein X represents sulphur or methylene, R, represents hydrogen, amino or an acylated or carbamylated amino group, R 2 represents hydrogen or an alkyl group and R 3 represents an alkoxy group; preparation thereof by subjecting a tripeptide of formula III, to the action of the enzyme isopenicillin N synthethase, and the tripeptide of formula III.
摘要:
The invention concerns an aminoquinoline-antibiotic hybrid compound of general formula (I): Q-(Y1)p-(U)p'-(Y2)p''-A; wherein Q represents an aminoquinoline, (Y1)p-(U)p'-(Y2)p'' is an optional spacer and A is an antibiotic residue. The invention enables the antibiotic residue activity to be unexpectedly enhanced.