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  2. Cefoperazone - Wikipedia

    en.wikipedia.org/wiki/Cefoperazone

    Cefoperazone contains an N-methylthiotetrazole (NMTT or 1-MTT) side chain.As the antibiotic is broken down in the body, it releases free NMTT, which can cause hypoprothrombinemia (likely due to inhibition of the enzyme vitamin K epoxide reductase) and a reaction with ethanol similar to that produced by disulfiram (Antabuse effect), due to inhibition of aldehyde dehydrogenase.

  3. Cefoperazone/sulbactam - Wikipedia

    en.wikipedia.org/wiki/Cefoperazone/sulbactam

    Cefoperazone/sulbactam is a combination drug used as an antibiotic. It is effective for the treatment of urinary tract infections . [ 2 ] It contains cefoperazone , a β-lactam antibiotic , and sulbactam , a β-lactamase inhibitor , which helps prevent bacteria from breaking down cefoperazone.

  4. Sulbactam - Wikipedia

    en.wikipedia.org/wiki/Sulbactam

    The combination cefoperazone/sulbactam (Sulperazon) is available in many countries but not in the United States. [4] The co-packaged combination sulbactam/durlobactam was approved for medical use in the United States in May 2023. [5]

  5. Cefamandole - Wikipedia

    en.wikipedia.org/wiki/Cefamandole

    Cefamandole (INN, also known as cephamandole) is a second-generation broad-spectrum cephalosporin antibiotic.The clinically used form of cefamandole is the formate ester cefamandole nafate, a prodrug which is administered parenterally.

  6. Cefbuperazone - Wikipedia

    en.wikipedia.org/wiki/Cefbuperazone

    This systemic antibiotic -related article is a stub. You can help Wikipedia by expanding it.

  7. Talk:Cefoperazone - Wikipedia

    en.wikipedia.org/wiki/Talk:Cefoperazone

    There are several relevent pubchem entries, each of which describe a unique species that is generally called "cefoperazone" or "cefoperazon". 44185 and 44187 are chiral isomers. 44185; 44186; 44187; 16052030 - sodium salt; 6420003-dihydrate; Fuzzform 22:52, 28 May 2007 (UTC)

  8. Cefmetazole - Wikipedia

    en.wikipedia.org/wiki/Cefmetazole

    The chemical structure of cefmetazole, like that of several other cephalosporins, contains an N-methylthiotetrazole (NMTT or 1-MTT) side chain.As the antibiotic is broken down in the body, it releases free NMTT, which can cause hypoprothrombinemia (likely due to inhibition of the enzyme vitamin K epoxide reductase) and a reaction with ethanol similar to that produced by disulfiram, due to ...

  9. Cefaclor - Wikipedia

    en.wikipedia.org/wiki/Cefaclor

    Cefaclor is frequently used against bacteria responsible for causing skin infections, otitis media, urinary tract infections, and others. Cefaclor has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections: Gram positive aerobes - Staphylococci (including coagulase-positive, coagulase-negative, and penicillinase-producing strains ...