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Cephalosporins with a 7 beta-[2-(5-amino-1,2,4-thiadiazol-3-yl) -2-oxyiminoacetamido] side chain were synthesized and their in vitro inhibitory potency was established. The compounds exhibit a strong antibacterial activity against various Gram-positive and Gram-negative bacteria. The antimicrobial activity is related to the oxime-substituent R1 and the C-3 substituent R2. Selected amino-1,2,4-thiadiazolyl-cephems 1 show a prolonged half-life in mice.
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CSENDES et al. (1983) studied this question.
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