When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Discovery and development of cephalosporins - Wikipedia

    en.wikipedia.org/wiki/Discovery_and_development...

    The basic structure of 3rd generation cephalosporins. The majority of third generation cephalosporins have the aminothiazole group at position C-7. Different groups are found at the 7-α-position like 7-α-iminohydroxy and 7-α-iminomethoxy groups. Ceftibuten however possesses a 7-α-ethylidene group. This group gives ceftibuten higher ...

  3. Cephalosporin - Wikipedia

    en.wikipedia.org/wiki/Cephalosporin

    Fourth-generation cephalosporins, however, have true broad-spectrum activity. [23] The classification of cephalosporins into "generations" is commonly practised, although the exact categorization is often imprecise. For example, the fourth generation of cephalosporins is not recognized as such in Japan.

  4. Cephalosporin C - Wikipedia

    en.wikipedia.org/wiki/Cephalosporin_C

    Cephalosporin C is an antibiotic of the cephalosporin class. It was isolated from a fungus of the genus Acremonium and first characterized in 1961. [ 1 ] Although not a very active antibiotic itself, synthetic analogs of cephalosporin C, such as cefalotin , became some of the first marketed cephalosporin antibiotic drugs.

  5. Cefuroxime axetil - Wikipedia

    en.wikipedia.org/wiki/Cefuroxime_axetil

    Cefuroxime axetil is a second generation cephalosporin that, like penicillins antibiotics, contains a β-lactam ring structure. Cephalosporins work as bactericidal antibiotics; that by binding to penicillin-binding proteins (PBPs), inhibit the last step of the bacterial cell wall synthesis. Once the β-lactam ring binds to PBPs, cross-linking ...

  6. 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 ...

  7. Cefadroxil - Wikipedia

    en.wikipedia.org/wiki/Cefadroxil

    Cefadroxil is a first-generation cephalosporin antibacterial drug that is the para-hydroxy derivative of cephalexin, and is used similarly in the treatment of mild to moderate susceptible infections such as the bacterium Streptococcus pyogenes, causing the disease popularly called strep throat or streptococcal tonsillitis, urinary tract infection, reproductive tract infection, and skin infections.

  8. Cefotiam - Wikipedia

    en.wikipedia.org/wiki/Cefotiam

    Cefotiam is a parenteral third-generation cephalosporin antibiotic. It has broad-spectrum activity against Gram-positive and Gram-negative bacteria. As a beta-lactam, its bactericidal activity results from the inhibition of cell wall synthesis via affinity for penicillin-binding proteins. It was patented in 1973 and approved for medical use in ...

  9. Flomoxef - Wikipedia

    en.wikipedia.org/wiki/Flomoxef

    Toggle the table of contents. Flomoxef. 9 languages. ... It has been classified either as a second-generation [1] or fourth-generation cephalosporin. [2]