Glycylcyclines: Difference between revisions
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| url = http://www.solen.cz/pdfs/far/2008/03/06.pdf
| url = http://www.solen.cz/pdfs/far/2008/03/06.pdf
| year = -2008
| year = -2008
| the_year = 3
| volume = 3
| volume = 22
| edition = 22
| pages = 113–115
| pages = 113–115
| issn = 1803-5353
| issn = 1803-5353

Revision as of 20:33, 26 January 2023

Glycylcyclines represent a new group of antibiotics that is derived from the tetracycline antibiotic minocycline. The main representative is tigecycline'. Tigecycline is a broad-spectrum ATB (effective against Gram-negative, Gram-positive and anaerobic microbes, but not effective against pseudomonads and proteums). Tigecycline is chemically a ``9-t-butylglycylamido derivative of minocycline.


Indication

They are indicated for complicated skin and soft tissue infections as well as intra-abdominal infections.

Mechanism of action

Their mechanism of action is: inhibition of proteosynthesis, (blocking of translation of protein in bacteria by binding to the ribosomal subunit 30S', blocks the entry of aminoacyl-tRNA molecules into the A site of the ribosome ).

Antimicrobial spectrum

It is a broad-spectrum antibiotic' that acts on many clinically important bacteria. Both gram-positive, gram-negative, anaerobic and atypical, including some multi-resistant, penicillin resistant Streptococcus pneumoniae, Klebsiella pneumoniae and Escherichia coli , Staphylococcus aureus, from gram-negative bacteria shows a lower sensitivity to Pseudomonas aeruginosa, Proteus mirabilis, Burkholderia cepacia and Stenotrophomonas malthophilia.

Side effects

Side effects are:


Links

Related articles

References