Aminopenicillin
From Wikipedia, the free encyclopedia
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 they contain a beta-lactam ring that is believed to be crucial to its antibacterial activity.
Aminopenicillins feature a positively charged amino group that enhances their uptake through bacterial porin channels. This does not, however, confer resistance to bacterial beta-lactamases.[2] Members of this family include ampicillin, amoxicillin and bacampicillin.[3]
See also[edit]
References[edit]
- ^ 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. Principles of Pharmacology. Philadelphia, PA: Lippincott Williams & Wilkins. ISBN 9781608312702.
- ^ "Mayo Clinic Proceedings". Retrieved 2008-12-26.[dead link]
 |
This systemic antibacterial-related article is a stub. You can help Wikipedia by expanding it. |
