Generalized structure of aminopenicillins
ampicillin

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.[citation needed]

Aminopenicillins feature a positively charged amino group that enhances their uptake through bacterial porin channels. This does not, however, prevent resistance conferred by bacterial beta-lactamases.[2] Members of this family include ampicillin, amoxicillin and bacampicillin.[3]

See also

References

  1. ^ Cunha BA (August 1992). "Aminopenicillins in urology". Urology. 40 (2): 186–90. doi:10.1016/0090-4295(92)90525-2. PMID 1502761.
  2. ^ Golan, David E. (2011-12-15). Principles of Pharmacology. Philadelphia, PA: Lippincott Williams & Wilkins. ISBN 9781608312702.
  3. ^ "Mayo Clinic Proceedings". Archived from the original on 2020-05-26. Retrieved 2008-12-26.


source: http://en.wikipedia.org/wiki/Aminopenicillin