Full list of author information is available at the end of the articleGlycylcyclines, are novel group of drugs which are tetracycline analogues that circumvent resistant mechanisms against tetracycline [1]. Tigecycline is the first member of the glycylcyclines group to be launched and acts on the ribosomes by inhibiting protein synthesis [2]. Tigecycline shows very good in vitro activity against Klebsiella pneumoniae and multi drug resistant (MDR) A. baumannii, it is also active against extended-spectrum beta-lactamase (ESBL) producing strains [1]. Tigecycline does not present cross-resistance with other antibiotics such as β lactams or fluoroquinolones [3]. A. baumannii has emerged as an important, troublesome nosocomial pathogen globally....
Tigecycline activity was evaluated against 11808 pathogens isolated from 30 US medical centers. Susc...
Full list of author information is available at the end of the articleto replace current available a...
Full list of author information is available at the end of the articleDespite the impressive scienti...
Tigecycline is a new glycylcycline antibiotic structurally similar to minocycline antibiotic. It has...
Aims: Acinetobacter species usually affect hospitalized patients and are involved in many infections...
Tigecycline is a novel glycylcycline that exhibits broad-spectrum antibacterial activity against a w...
Tigecycline is unique glycylcycline class of semisynthetic antimicrobial agents developed for the tr...
bS Supporting Information ABSTRACT: A novel series of fully synthetic 8-azatetracyclines was prepare...
Purpose: Tigecycline, a glycylcycline antibiotic is a promising option for the treatment of single o...
New antimicrobial agents are urgently needed for clinical use due to the increasing prevalence and s...
Tigecycline, a semisynthetic derivative of minocycline, has a broad spectrum of activity against bot...
Tigecycline is a semisynthetic analogue of earlier tetracyclines and represents the first member of ...
The increasing antimicrobial resistance found in the many clinically important species of bacteria t...
Full list of author information is available at the end of the articleIntroduction Fluoroquinolones ...
The in vitro activity of tigecycline (former GAR-936), a new semisynthetic tetracycline, was evaluat...
Tigecycline activity was evaluated against 11808 pathogens isolated from 30 US medical centers. Susc...
Full list of author information is available at the end of the articleto replace current available a...
Full list of author information is available at the end of the articleDespite the impressive scienti...
Tigecycline is a new glycylcycline antibiotic structurally similar to minocycline antibiotic. It has...
Aims: Acinetobacter species usually affect hospitalized patients and are involved in many infections...
Tigecycline is a novel glycylcycline that exhibits broad-spectrum antibacterial activity against a w...
Tigecycline is unique glycylcycline class of semisynthetic antimicrobial agents developed for the tr...
bS Supporting Information ABSTRACT: A novel series of fully synthetic 8-azatetracyclines was prepare...
Purpose: Tigecycline, a glycylcycline antibiotic is a promising option for the treatment of single o...
New antimicrobial agents are urgently needed for clinical use due to the increasing prevalence and s...
Tigecycline, a semisynthetic derivative of minocycline, has a broad spectrum of activity against bot...
Tigecycline is a semisynthetic analogue of earlier tetracyclines and represents the first member of ...
The increasing antimicrobial resistance found in the many clinically important species of bacteria t...
Full list of author information is available at the end of the articleIntroduction Fluoroquinolones ...
The in vitro activity of tigecycline (former GAR-936), a new semisynthetic tetracycline, was evaluat...
Tigecycline activity was evaluated against 11808 pathogens isolated from 30 US medical centers. Susc...
Full list of author information is available at the end of the articleto replace current available a...
Full list of author information is available at the end of the articleDespite the impressive scienti...