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  2. Prokaryotic small ribosomal subunit - Wikipedia

    en.wikipedia.org/wiki/Prokaryotic_small...

    The 30S subunit is the target of antibiotics such as tetracycline and gentamicin. [11] These antibiotics specifically target the prokaryotic ribosomes, hence their usefulness in treating bacterial infections in eukaryotes. Tetracycline interacts with H27 in the small subunit as well as binding to the A-site in the large subunit. [11]

  3. Tetracycline antibiotics - Wikipedia

    en.wikipedia.org/wiki/Tetracycline_antibiotics

    They inhibit protein synthesis by binding reversibly to the bacterial 30S ribosomal subunit and preventing the aminoacyl tRNA from binding to the A site of the ribosome. They also bind to some extent the bacterial 50S ribosomal subunit and may alter the cytoplasmic membrane causing intracellular components to leak from bacterial cells.

  4. Antibiotic - Wikipedia

    en.wikipedia.org/wiki/Antibiotic

    Most target bacterial functions or growth processes. [8] Those that target the bacterial cell wall (penicillins and cephalosporins) or the cell membrane , or interfere with essential bacterial enzymes (rifamycins, lipiarmycins, quinolones, and sulfonamides) have bactericidal activities, killing the bacteria.

  5. List of antibiotics - Wikipedia

    en.wikipedia.org/wiki/List_of_antibiotics

    Inhibits bacterial protein synthesis by binding to the 50S subunit of the ribosome Fosfomycin: Monurol, Monuril: Acute cystitis in women: This antibiotic is not recommended for children and 75 and up of age: Inactivates enolpyruvyl transferase, thereby blocking cell wall synthesis Fusidic acid: Fucidin: Metronidazole: Flagyl

  6. Cresomycin - Wikipedia

    en.wikipedia.org/wiki/Cresomycin

    Cresomycin has been found to effective against bacteria that are resistant to multible antibiotics, including lincosamides, both in vitro and in vivo, being more potent than iboxamycin. [1] The antibiotic was found in time-kill studies to be bacteriostatic against S. aureus. In vitro safety experiments with human cells indicated low ...

  7. Beta-lactamase - Wikipedia

    en.wikipedia.org/wiki/Beta-lactamase

    The two types of beta-lactamases work on the basis of the two basic mechanisms of opening the β-lactam ring. [2]The SBLs are similar in structure and mechanistically to the β-lactam target penicillin-binding proteins (PBPs) which are necessary for cell wall building and modifying.

  8. Doxycycline - Wikipedia

    en.wikipedia.org/wiki/Doxycycline

    Doxycycline, like other tetracycline antibiotics, is bacteriostatic. It works by preventing bacteria from reproducing by inhibiting protein synthesis. [80] Doxycycline is highly lipophilic, so it can easily enter cells, meaning the drug is easily absorbed after oral administration and has a large volume of distribution.

  9. Streptomycin - Wikipedia

    en.wikipedia.org/wiki/Streptomycin

    As human and bacteria both have ribosomes, streptomycin has significant side effects in humans. At low concentrations, however, streptomycin inhibits only bacterial growth. [18] Streptomycin is an antibiotic that inhibits both Gram-positive and Gram-negative bacteria, [19] and is therefore a useful broad-spectrum antibiotic.