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  2. Ceftriaxone - Wikipedia

    en.wikipedia.org/wiki/Ceftriaxone

    Ceftriaxone, sold under the brand name Rocephin, is a third-generation cephalosporin antibiotic used for the treatment of a number of bacterial infections. [4] These include middle ear infections, endocarditis, meningitis, pneumonia, bone and joint infections, intra-abdominal infections, skin infections, urinary tract infections, gonorrhea, and pelvic inflammatory disease. [4]

  3. PubChem - Wikipedia

    en.wikipedia.org/wiki/PubChem

    PubChem is a database of chemical molecules and their activities against biological assays. The system is maintained by the National Center for Biotechnology Information (NCBI), a component of the National Library of Medicine , which is part of the United States National Institutes of Health (NIH).

  4. Ceftriaxone sodium - Wikipedia

    en.wikipedia.org/?title=Ceftriaxone_sodium&...

    From Wikipedia, the free encyclopedia. Redirect page

  5. Cefuroxime - Wikipedia

    en.wikipedia.org/wiki/Cefuroxime

    Cefuroxime is active against many bacteria including susceptible strains of Staphylococci and Streptococci, as well as a range of gram negative organisms. [11] As with the other cephalosporins, it is susceptible to beta-lactamase, although as a second-generation variety, it is less so.

  6. p-Cresol - Wikipedia

    en.wikipedia.org/wiki/P-cresol

    This residue contains a few percent by weight of phenol and cresols. Industrially, p-cresol is currently prepared mainly by a two-step route beginning with the sulfonation of toluene: [4] CH 3 C 6 H 5 + H 2 SO 4 → CH 3 C 6 H 4 SO 3 H + H 2 O. Basic hydrolysis of the sulfonate salt gives the sodium salt of the cresol: CH 3 C 6 H 4 SO 3 H + 2 ...

  7. Cefoxitin - Wikipedia

    en.wikipedia.org/wiki/Cefoxitin

    Cefoxitin is a beta-lactam antibiotic which binds to penicillin binding proteins, or transpeptidases. By binding to PBPs, cefoxitin prevents the PBPs from forming the cross-linkages between the peptidoglycan layers that make up the bacterial cell wall, thereby interfering with cell wall synthesis.

  8. Cefditoren - Wikipedia

    en.wikipedia.org/wiki/Cefditoren

    The most frequent adverse drug reaction was diarrhea (1.30%) that resolved or subsided during treatment or after discontinuation or completion of therapy in all cases. [ 14 ] Data from the clinical studies carried out with cefditoren in the treatment of pharyngotonsillitis from 2007 to 2010 in Japan showed that the percentage of adverse events ...

  9. Ceftiofur - Wikipedia

    en.wikipedia.org/wiki/Ceftiofur

    Ceftiofur is an antibiotic of the cephalosporin type (third generation), licensed for use in veterinary medicine.It was first described in 1987. [3] It is marketed by pharmaceutical company Zoetis as Excenel, [4] Naxcel, and Excede and is also the active ingredient in that company's Spectramast LC (lactating cow formulation) and Spectramast DC (dry cow formulation) product.