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  2. Aminoglycoside - Wikipedia

    en.wikipedia.org/wiki/Aminoglycoside

    Streptomycin. 2D line-angle representation.. Aminoglycoside is a medicinal and bacteriologic category of traditional Gram-negative antibacterial medications that inhibit protein synthesis and contain as a portion of the molecule an amino-modified glycoside ().

  3. Protein synthesis inhibitor - Wikipedia

    en.wikipedia.org/wiki/Protein_synthesis_inhibitor

    Chloramphenicol blocks the peptidyl transfer step of elongation on the 50S ribosomal subunit in both bacteria and mitochondria.; Macrolides (as well as inhibiting ribosomal translocation [8] and other potential mechanisms) bind to the 50s ribosomal subunits, inhibiting peptidyl transfer.

  4. 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]

  5. Lincosamides - Wikipedia

    en.wikipedia.org/wiki/Lincosamides

    Of the lincosamides, clindamycin is most commonly used within the clinic due to its higher bioavailability, higher oral absorption and efficacy within the target organism spectrum. [23] Lincosamides are generally the first-choice use antibiotic class in veterinary microbiology, most commonly used to combat skin infections.

  6. Tetracycline antibiotics - Wikipedia

    en.wikipedia.org/wiki/Tetracycline_antibiotics

    Tetracycline antibiotics are protein synthesis inhibitors. [22] They inhibit the initiation of translation in variety of ways by binding to the 30S ribosomal subunit, which is made up of 16S rRNA and 21 proteins. They inhibit the binding of aminoacyl-tRNA to the mRNA translation complex.

  7. Aminocoumarin - Wikipedia

    en.wikipedia.org/wiki/Aminocoumarin

    Aminocoumarin is a class of antibiotics that act by an inhibition of the DNA gyrase enzyme involved in the cell division in bacteria. They are derived from Streptomyces species, [1] whose best-known representative – Streptomyces coelicolor – was completely sequenced in 2002. [2] The aminocoumarin antibiotics include: [3]

  8. New antibiotic uses novel method to target deadly drug ... - AOL

    www.aol.com/news/antibiotic-uses-novel-method...

    Scientists say they have developed a new type of antibiotic to treat a bacteria that is resistant to most current antibiotics and kills a large percentage of people with an invasive infection.

  9. List of antibiotics - Wikipedia

    en.wikipedia.org/wiki/List_of_antibiotics

    Antibiotics with less reliable but occasional (depending on isolate and subspecies) activity: occasionally penicillins including penicillin, ampicillin and ampicillin-sulbactam, amoxicillin and amoxicillin-clavulnate, and piperacillin-tazobactam (not all vancomycin-resistant Enterococcus isolates are resistant to penicillin and ampicillin)