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  2. Ampicillin - Wikipedia

    en.wikipedia.org/wiki/Ampicillin

    Ampicillin is an antibiotic belonging to the aminopenicillin class of the penicillin family. The drug is used to prevent and treat several bacterial infections , such as respiratory tract infections , urinary tract infections , meningitis , salmonellosis , and endocarditis . [ 7 ]

  3. β-Lactam antibiotic - Wikipedia

    en.wikipedia.org/wiki/Β-Lactam_antibiotic

    This resistance mechanism underscores the importance of the structural integrity of the β-lactam ring for the antibiotic's function. [24] The color change from colorless or light yellow to amber or even red in an aqueous solution of a β-lactam antibiotic can denote β-lactamase hydrolysis of amide bonds in the β-lactam ring.

  4. Ampicillin/sulbactam - Wikipedia

    en.wikipedia.org/wiki/Ampicillin/sulbactam

    Ampicillin/sulbactam is a combination of a β-lactam antibiotic and a β-lactamase inhibitor. Ampicillin works by binding to penicillin-binding proteins (PBPs) to inhibit bacterial cell wall synthesis. [13] [14] This causes disruption of the bacterial cell wall and leads to bacterial cell death.

  5. Penicillin - Wikipedia

    en.wikipedia.org/wiki/Penicillin

    Penicillin molecules are small enough to pass through the spaces of glycoproteins in the cell wall. For this reason Gram-positive bacteria are very susceptible to penicillin (as first evidenced by the discovery of penicillin in 1928 [46]). [47] Penicillin, or any other molecule, enters Gram-negative bacteria in a different manner. The bacteria ...

  6. 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. SBLs and PBPs both covalently change an active site serine ...

  7. Aminopenicillin - Wikipedia

    en.wikipedia.org/wiki/Aminopenicillin

    The aminopenicillins are a group of antibiotics in the penicillin family that are structural analogs of ampicillin (which is the 2-amino derivative of benzylpenicillin, hence the name). [1] Like other penicillins and beta-lactam antibiotics , they contain a beta-lactam ring that is crucial to its antibacterial activity.

  8. List of antibiotics - Wikipedia

    en.wikipedia.org/wiki/List_of_antibiotics

    Wide range of infections; penicillin used for streptococcal infections, syphilis, and Lyme disease: Gastrointestinal upset and diarrhea; Allergy with serious anaphylactic reactions; Brain and kidney damage (rare) Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls ...

  9. Antibiotic - Wikipedia

    en.wikipedia.org/wiki/Antibiotic

    The chemical structure of penicillin was first proposed by Abraham in 1942 [151] and then later confirmed by Dorothy Crowfoot Hodgkin in 1945. Purified penicillin displayed potent antibacterial activity against a wide range of bacteria and had low toxicity in humans.