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Chemical Compound Review

CHEMBL472175     (6R,7R)-7-[[(2Z)-2-(5-amino- 1,2,4...

Synonyms: AC1NUZ4P, AKOS015950773, BCP9000505, AB1004831, 113359-04-9, ...
This record was replaced with 6858015.
 
 
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Disease relevance of SCE 2787

  • In addition, 20 g showed activity similar or slightly inferior to that of CZOP against Pseudomonas aeruginosa both in vitro and in vivo [1].
  • In an effort to discover a novel cefozopran (CZOP) derivative having excellent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA), we performed chemical modification of the alkoxyimino moiety and imidazo[1,2-b]pyridazinium group of CZOP [1].
 

High impact information on SCE 2787

  • BACKGROUND AND METHODS: We compared the bacteriological, pharmacological and histopathological effects of parenterally administered ciprofloxacin (CPFX) to those of imipenem/cilastatin (IMP/CS) and cefozopran (CZOP) in a murine model of mucoid Pseudomonas aeruginosa pneumonia mimicking ventilator-associated pneumonia [2].
 

Analytical, diagnostic and therapeutic context of SCE 2787

References

  1. Studies on anti-MRSA parenteral cephalosporins. II. Synthesis and antibacterial activity of 7beta-[2-(5-amino-1,2,4- thiadiazol-3-yl)-2(Z)-alkoxyiminoacetamido]-3-(substituted imidaz. Ishikawa, T., Kamiyama, K., Matsunaga, N., Tawada, H., Iizawa, Y., Okonogi, K., Miyake, A. J. Antibiot. (2000) [Pubmed]
  2. Effects of parenterally administered ciprofloxacin in a murine model of pulmonary Pseudomonas aeruginosa infection mimicking ventilator-associated pneumonia. Kaneko, Y., Yanagihara, K., Kuroki, M., Ohi, H., Kakeya, H., Miyazaki, Y., Higashiyama, Y., Hirakata, Y., Tomono, K., Kadota, J.I., Kohno, S. Chemotherapy. (2001) [Pubmed]
 
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