Chemistry:Aminopenicillin
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Short description: Group of antibiotics
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
- ↑ Cunha BA (August 1992). "Aminopenicillins in urology". Urology 40 (2): 186–90. doi:10.1016/0090-4295(92)90525-2. PMID 1502761.
- ↑ Golan, David E. (2011-12-15). Principles of Pharmacology. Philadelphia, PA: Lippincott Williams & Wilkins. ISBN 9781608312702.
- ↑ "Mayo Clinic Proceedings". http://www.mayoclinicproceedings.com/inside.asp?AID=2547.
Original source: https://en.wikipedia.org/wiki/Aminopenicillin.
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